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* Nome italiano[Sinonimi]•Nome inglese[Synonyms]•Nome francese[Synonymes]•Nome spagnolo[Sinónimos]•{n.indice OMIM}•<Vedi legenda >

 

M
* Maaswinkel Mooij Stokvis Brantsma Sindrome di••Maaswinkel mooij stokvis brantsma syndrome de••{}
* MacDermot Patton Williams Sindrome di•Hypertrichosis cubiti•Mac dermot patton williams syndrome de[Hypertrichose cubitale petite taille]••{139600}
* MacDermot Winter Sindrome di•MacDermot-Winter syndrome•Mac dermot winter syndrome de••{247900}
* Maccario Mena Sindrome di••Maccario mena syndrome de[Neuroaxonale dystrophie acidose tubulaire]••{}
* Machado-Joseph Malattia di••Machado-Joseph, maladie de[Ataxie spinocérébelleuse autosomique dominante/ Ataxie cérébelleuse autosomique dominante]•Machado Joseph, Enfermedad de•{109150-117200-117210-117400-183086-183090-212900-600223-600224-603680}
* Macchie caffe' latte Sindrome••••{}
* Macias Flores Garcia Cruz Sindrome di••Macias flores garcia cruz syndrome de[Hypertrichose generalisee liee a l x]••{307150}
* Mackay Shek Carr Sindrome di••Mackay shek carr syndrome de[Degenerescence retinienne microphtalmie glaucome]••{267760}
* Macleod Fraser Sindrome di••Macleod fraser syndrome de[Micromelie retard mental myopie]••{}
* Macrocefalia(//)

/Macrocefalia amartoma mesodermico Sindrome con

/Macrocefalia anomalie della pigmentazione, estremità grosse

/Macrocefalia arti corti sordità

/Macrocefalia bassa statura paraplegia

/Macrocefalia dominante

/Macrocefalia mesomelia piedi torti

/Macrocefalia ritardo mentale dismorfismi facciali

•macrocephaly with feeblemindedness and encephalopathy with peculiar deposits

macrocephaly-cutis marmorata telangiectatica congenita syndrome

macrocephaly-facial abnormalities-disproportionate tall stature-mental retardation syndrome

macrocephaly-hamartomas syndrome

macrocephaly-hypertelorism-short limbs-hearing loss-developmental delay syndrome

macrocephaly-multiple lipomas-hemangiomata syndrome

macrocephaly-pseudoepithelioma-multiple hemangiomas syndrome

•Macrocephalie hamartome mesodermique syndrome

Macrocephalie membres courts surdite

Macrocephalie mesomelie pieds bots

Macrocephalie petite taille paraplegie

Macrocephalie pigmentation anomalies extremites grandes

Macrocephalie retard mental dysmorphie faciale

•Macrocefalia, Lipomas y Hamartomas Múltiples

Macrocefalia, Pseudopapiledema y Hamartomas Múltiples

•{}
* Macrocefalia dominante••Macrocephalie dominante[Megalencephalie familiale]••{153470}
* Macroglobulinemia[Malattia di Waldenstrom/Macroglobulinemia essenziale]•••Macroglobulinemia[Waldenstrom, Síndrome de]•{}
* Macroglossia dominante[Lingua gigante/Macroglossia gigante]•Macroglossia[Enlarged Tongue/Giant Tongue]•Macroglossie dominante••{153630}
* Macropoliadenomatosi surrenale••Macropolyadénomatose surrénalienne i[Syndrome de Cushing familial]••{}
* Macrotrombocitopenia sordità progressiva[Sindrome di Bertrand-Soulier/Deficit del fattore recettore Von Willebrand]•[Giant platelet syndrome/ Bernard-Soulier Syndrome/BSS/Platelet Glycoprotein Ib, Deficiency of/Glycoprotein Ib, platelet, Alpha polypeptide/GP1BA/GP Ib, Alpha subunit/Glycocalicin/Platelet Glycoprotein Ib, polymorphism of/Von Willebrand factor receptor, deficiency of/Macrothrobocytopenia, familial, Bernard-Soulier Type/Von Willebrand disease, platelet Type/Bernard-Soulier Syndrome, autosomal dominant/Bernard-Soulier Syndrome, Type A]•Macrothrombocytopenie surdite progressive•Macrotrombocitopenia Familiar, Tipo Bernard Soulier Hemorrágica/Glicoproteína Plaquetaria Ib,[Bernard Soulier, Síndrome de/Distrófia Trombocitopénica Déficit de la/Glicoproteína Plaquetaria Ib, Polimorfismo de la/Factor Receptor de Von Willebrand, Déficit de]•{231200}
* Madelung Malattia di[Lipomatosi multipla simmetrica]•Madelung's Disease•Madelung, maladie de•Madelung, Enfermedad de[ Lipomatosis Cervical Simétrica Benigna/Lipomatosis Cervical Simétrica Múltiple/Launois Bensaude, Síndrome de]•{151800}
* Madokoro Ohdo Sonoda Sindrome di••Madokoro ohdo sonoda syndrome de••{}
* Maestre de San Juan-Kallmann-de Morsier Sindrome di[Ipogonadismo-anosmia Sindrome/Displasia olfattogenitale]•Maestre de San Juan-Kallmann-de Morsier syndrome[Kallmann syndrome 3/de Morsier syndrome/de Morsier-Gauthier syndrome/Kallmann-de Morsier syndrome/Maestre-Kallmann-de Morsier syndrome/Mastre de San Juan-Kallmann syndrome/congenital anosmia-hypogonadotropic hypogonadism syndrome/hypogonadism-anosmia syndrome/hypogonadotropic hypogonadism-anosmia (HHA) syndrome/hyposmia-hypogonadotropic hypogonadism syndrome/idiopathic hypothalamic hypogonadism (IHH)/olfacto-ethmoidohypothalamic dysplasia/olfacto-ethmoidodypothalamic dysraphia/olfactogenital dysplasia/olfactogenital syndrome]•••{244200-308700}
* MAFFUCCI SINDROME DI/Maffucci Malattia di[Discondroplasia con emangiomi/Condrodistrofia con amartomi vascolari/Sindrome di Kast/Sindrome di Maffucci-Kast/Discondroplasia, discromia cutanea]•Maffucci Syndrome•Maffucci, maladie de••{166000}•S•M
* Magersucht Sindrome di•••Magersucht, Síndrome de•{}
* Maghazaji Sindrome di••Maghazaji syndrome de••{}
* Majewski Ozturk Sindrome dii••Majewski ozturk syndrome de••{}
* Malaria[Paludismo]•Malaria•Paludisme•Malaria[M. Aguda/M. Autóctona/M. Crónica/M. Intermitente/Paludismo]•{-}
* MALASSORBIMENTO CONGENITO DI SACCAROSIO ED ISOMALTOSIO•Sucrose Isomaltose Malabsorption, Congenital[Disaccharide Intolerance I SI Deficiency/Sucrase-Isomaltase Deficiency, Congenital/Sucrose Intolerance, Congenital/CSID]••Malabsorción Congénita de Sucrosa Isomaltosa•{}
* Malassorbimento del Triptofano Sindrome del•••Malabsorción del Triptofano, Síndrome de[Drummond, Síndrome de/Hipercalcemia Familiar con Nefrocalcinosis e Indicanuria/Pañal Azul, Síndrome de]•{}
* Malattia celiaca => Vedi Celiachia
* MALATTIA DA INCLUSIONE DEI MICROVILLI••{251850}
* MALATTIA DEL FEGATO POLICISTICO•Polycystic Liver Disease•••{}
* Malattia del Rene Policistico/M R P Autosomica Dominante/M. R. P. Autosomica Recessiva/Rene policistico tipo adulto/Rene policistico tipo dominante/Rene policistico tipo infantile/Rene policistico tipo recessivo •Polycystic Kidney Diseases•••{}
* MALATTIA DELLE URINE A SCIROPPO DI ACERO•Maple Syrup Urine Disease•Sirop d'érable, maladie du••{}
* MALATTIA DI GAUCHER•Gaucher Disease•Gaucher, maladie de••{230800}•D•A

MALATTIA GRANULOMATOSA CRONICA/MALATTIA GRANULOMATOSA CRONICA••••{306400}
* MALATTIA DI HUNTINGTON••••{}
* Malattie Lisosomiali•Lysosomal Storage Diseases•••{}
* Malattia periodica =>Vedi Febbre Mediterranea Familiare
* MALATTIE SPINOCEREBELLARI••••{}
* Malattie Metaboliche Ereditarie••••{}•S•A
* Mallory Weiss Sindrome di[Lacerazioni della mucosa dell'esofago o del giunto gastroesofageo/Sindrome di lacerazione gastroesofagea-emorragica]•Mallory Weiss Syndrome••Mallory Weiss, Síndrome de•{}
* Malouf Sindrome di•Malouf syndrome•Malouf syndrome de••{}
* Malpuech Sindrome di•Malpuech syndrome[Facial clefting syndrome, Gypsy type]•••{248340}
* Malpuech Demeocq Palcoux Sindrome di••Malpuech demeocq palcoux syndrome de••{}
* Mani e piedi assenza••Absence de mains et pieds••{}
* Mani e piedi a specchio anomalie del naso••••{}
* Mani e piedi, deformazioni delle, faccia piatta••••{}
* Mano-piede-utero Sindrome••••{}
* Mano Schisi della, agenesia della tibia••••{}
* Marashi Gorlin Sindrome di••Marashi gorlin syndrome de••{}
* Marchiafava-Micheli Malattia di[Degenerazione primitiva del corpo calloso/Encefalopatia demielinizzante del calloso/Malattia di Marchiafava/Degenerazione trabeale degli alcolisti]•••Marchiafava Bignami, Enfermedad de[Enfermedad de Marchiafava/Degeneración Primaria del Cuerpo Calloso/Degeneración del Cuerpo Calloso, Síndrome de]•{}
* MARCHIAFAVA-MICHELI SINDROME DI[Emoglobinuria parossistica notturna /Anemia emolitica tipo Marchiafava/sindrome di Marchiafava-Nazari-Micheli/Sindrome di Strubing-Marchiafava]••Marchiafava-Micheli, maladie de•Marchiafava Michelli, Síndrome de•{311770}
* Marden Walker-like Sindrome di•Marden Walker Syndrome/Marden-Walker syndrome (MWS)•Marden walker syndrome de•Marden Walker, Síndrome de•{}
* MARFAN SINDROME DI/Marfan Sindrome di•Marfan Syndrome•Marfan, syndrome de•Marfan, Síndrome de•{154700}•D•A
* Marie-Sainton Sindrome di[Disostosi cleidocranica ereditaria/Sindrome di Scheuthaurer/Sindrome di Hulkcrantz/Disostosi cleido-cranio-dentaria/Displasia osteodentaria]•Marie-Sainton syndrome••Marie Sainton, Enfermedad de•{}
* Marie Strumpell Malattia di[Spondilosi rizomelica]•Marie-Strumpell Spondylitis[Ankylosing Spondylitis/AS/Bechchterew Syndrome]••Marie Strumpell, Enfermedad de[Bechterew, Síndrome de/Espondilitis de MarieStrumpell/Von Bechterew Strumpell, Síndrome de/Espondilitis Anquilopoyética]•{106300}
* Marie-Tooth Malattia di=>Vedi Charcot-MarieTooth Malattia
* MARINESCO-SJOGREN SINDROME DI/Marinesco-Sjogren Sindrome di[Degenerazione cerebellare oligofrenica ereditaria/Sindrome cataratta-oligofrenia/Sindrome di Garland-Moorhause/Sindrome di Marinesco-Garland/Sindrome di Sjogren/Sindrome cataratta-oligofrenia]•Marinesco Sjogren Syndrome/Marinesco-Sjögren-Garland syndrome[Marinesco-Sjögrensyndrome/MSS/ Marinesco-Garland syndrome/Torsten Sjögren syndrome/cataract-oligophrenia syndrome/hereditary oligophrenic cerebellolental degeneration]••{248800}
* Marinesco Sjogren-like Sindrome (MSLS)•Marinesco-Sjögren-like syndrome (MSLS)•Marinesco sjogren like syndrome de••{}
* Marion Mayers Sindrome di••Marion mayers syndrome de••{}
* Markel Vikkula Mulliken Sindrome di[Malformazioni venose familiari]• Malformations, Multiple Cutaneous and mucosal/VMCM•Markel vikkula mulliken syndrome de[Malformations veineuses familiales]••{600195}
* Marles Greenberg Persaud Sindrome di••Marles greenberg persaud syndrome de••{}
* Maroteaux Cohen Solal Bonaventure Sindrome di••Maroteaux cohen solal bonaventure syndrome de••{}
* Maroteaux Fonfria Sindrome di••Maroteaux fonfria syndrome de••{}
* Maroteaux-Lamy Malattia di•Maroteaux-Lamy disease/Maroteaux Lamy Syndrome•••{}
* Maroteaux Le Merrer Bensahel Sindrome di••Maroteaux le merrer bensahel syndrome de••{}
* Maroteaux-Malamut Sindrome di•Maroteaux-Malamut syndrome•••{}
* Maroteaux Stanescu Cousin Sindrome di••Maroteaux stanescu cousin syndrome de••{}
* Maroteaux Verloes Stanescu Sindrome di••Maroteaux verloes stanescu syndrome de••{}
* MAROTEAUX-LAMY SINDROME DI•Maroteaux Lamy Syndrome/Maroteaux-Lamy syndrome•Maroteaux-Lamy, maladie de•Maroteaux Lamy, Síndrome de•{}
* Marsden Nyhan Sakati Sindrome di••Marsden nyhan sakati syndrome de••{}
* MARSHALL SINDROME DI/Marshall Sindrome di•Marshall Syndrome/Marshall syndrome•Marshall, syndrome de•Marshall, Síndrome de•{154780}
* MARSHALL-SMITH SINDROME DI/Marshall-Smith Sindrome di•Marshall Smith Syndrome/Marshall-Smith syndrome (MSS)/Marshall-Smith-Weaver syndrome/Marshall-Weaver syndrome•Marshall-Smith, syndrome de•Marshall Smith, Síndrome de•{602535}
* Marsolf Sindrome di•Martsolf syndrome•Marsolf syndrome de••{}
* Martin Bell, Sindrome di/Fra-X sindrome/X fragile, sindrome dell'[FRAXA/FRAXE/Ritardo Mentale X-fragile/FraX/X SINDROME DA X FRAGILE]•Fragile X Syndrome/Martin-Bell syndrome (MBS)•X fragile, syndrome de l'[Fra-X syndrome]•Martin Bell, Síndrome de[X Frágil, Síndrome]•{309550-309548}•D•S
* Martin-Bell-Renpenning Sindrome di•Martin-Bell-Renpenning syndrome•••{}
* Martinez Monasterio Pinheiro Sindrome di••Martinez monasterio pinheiro syndrome de••{}
* Martorell Sindrome di•••Martorell, Síndrome de•{}
* Martsolf Reed Hunter Sindrome di••Martsolf reed hunter syndrome de[Pierre robin nanisme polydactylie]••{}
* MASA sindrome•MASA Syndrome[Mental retardation, Aphasia, Shuffling gait, and Adducted thumbs/Gareis-Mason Syndrome]•MASA syndrome•MASA, Síndrome de[Retraso Mental y Pulgares en Adducción, ligado al Cromosoma X, Síndrome de/Pulgares en adducción y Retraso Mental/Retraso Mental, Afasia, Marcha Arrastrando los Pies y Pulgares en Adducción/Garies Mason, Síndrome de/Pulgar en Garra Congénito con Retraso Mental]•{303350}
* Massa Casaer Ceulemans Sindrome di••Massa casaer ceulemans syndrome de••{}
* Mastocitosi ereditaria•Mastocytosis•Mastocytose systémique••{154800}•D
* Mastocitosi midollare••••{}
* Mastre de San Juan-Kallmann Sindrome di•Mastre de San Juan-Kallmann syndrome•••{}
* Mastroiacovo De Rosa Satta Sindrome di••Mastroiacovo de rosa satta syndrome de••{}
* Mastroiacovo Gambi Segni Sindrome di••Mastroiacovo gambi segni syndrome de••{}
* Mathieu De Broca Bony Sindrome di••Mathieu de broca bony syndrome de••{}
* Matsoukas Liarikos Giannika Sindrome di••Matsoukas liarikos giannika syndrome de••{}
* Maxillo nasale tipo Binder Displasia•Maxillonasal Dysplasia, Binder Type•Maxillo nasale dysplasie type binder••{}
* Maxillofacciale Disostosi•Maxillofacial Dysostosis•••{}
* May Hegglin Anomalia[Sindrome mielopatica a corpi di Dohle]•May Hegglin Anomaly•••{}
* Mayer Rokitansky Kuster Hauser Sindrome di[Anomalia MRK/Atresia utero-vaginale congenita/Ipoplasia o assenza congenita della vagina associata a qualche forma di utero rudimentale, anormale o assente/Uterus bicornis rudimentarius/Uterus bipartitus solidus rudimentarius cum vagina solida/Sindrome di Rokitansky/Sindrome di Rokitansky-Kuster-Hauser(Sindrome RKH)]•Mullerian Aplasia•Absence congenitale d uterus et de vagin•Mayer Rokitansky Kuster Hauser, Síndrome de[Aplasia Mulleriana]•{277000-158330-266810}•S
* McAlister Coe White Sindrome di••Mcalister coe white syndrome de••{277000}
* McAlister Crane Sindrome di••Mcalister crane syndrome de••{}
* McArdle Malattia di•McArdle Disease••McArdle, Enfermedad de[Depósito de Glucógeno Tipo V, Enfermedad por/Miofosforilasa, Déficit de/Glucogenosis Tipo V]•{232600}
* McCallum Macadam Johnston Sindrome di••Mccallum macadam johnston syndrome de••{}
* MCCUNE-ALBRIGHT SINDROME DI/McCune-Albright, Sindrome di/McCune-Albright Sindrome di[Sindrome di Albright/Osteosi Fibrosa Diffusa PFD/Displasia Fibrosa Poliostotica/OSTEITE FIBROSA DISSEMINATA/POFD/Sindrome di Fuller-Albright/sindrome di Albright-McCune-Sternberg/Pubertà precoce con fibrosi poliostotica e pigmentazione non normale]•McCune Albright SyndromeMAS[Polyostic Fibrous Dysplasia/PFD/POFD/ Albright Syndrome]•McCune-Albright, syndrome de•McCune Albright, Síndrome de[Displasia Fibrosa/Displasia Monostótica Fibrosa/Displasia Fibrosa Poliostótica/Jaffe Lichenstein, Enfermedad de/Osteofibrosis/Displasia Fibrosa Juvenil]•{}•A•S
* McDonough Sindrome di••Mcdonough syndrome de•McDonough syndrome•{}
* McDowal Sindrome di••Mcdowal syndrome de••{}
* McGillivray Sindrome di••Mcgillivray syndrome de••{}
* McKusick Kaufman Sindrome di••Mckusick kaufman syndrome de••{}
* McLain Debakian Sindrome di••Mclain debakian syndrome de••{}
* McPherson Clemens Sindrome di••Mcpherson clemens syndrome de••{}
* Mcpherson Robertson Cammarano Sindrome di••Mcpherson robertson cammarano syndrome de••{}
* Meacham Winn Culler Sindrome di••Meacham winn culler syndrome de••{}
* Meadows Sindrome di•Meadow syndrome•Meadows syndrome de••{}
* MEB (Muscle-Eye-Brain) Sindrome••MEB (Muscle-Eye-Brain) syndrome[Syndrome muscle-oeil-cerveau]••{}
* MECKEL SINDROME DI/Meckel Sindrome di[Disencefalia splancnocistica]•Meckel Syndrome•Meckel, syndrome de•Meckel, Síndrome de[Disencefalia Esplacnocística/Meckel Gruber, Síndrome de/Gruber, Síndrome de]•{249000-603194}
* Meckel-like Sindrome••Meckel like syndrome••{}
* Medeira Dennis Donnai Sindrome di••Medeira dennis donnai syndrome de••{}
* Medokoro Ohdo Sonoda Sindrome di••Madokoro ohdo sonoda syndrome de••{}
* Medrano Roldan Sindrome di••Medrano roldan syndrome de••{}
* Medulloblastoma•Medulloblastoma•Médulloblastome••{}
* MEESMANN DISTROFIA DI[DISTROFIA CORNEALE EPITELIALE GIOVANILE]••••{}
* Mehes Sindrome di••Mehes syndrome de[Retard de langage asymetrie faciale strabisme incisure du lobe]••{182875}
* Meier Gorlin Sindrome di[Microtia, assenza rotula, micrognatia Sindrome/Microtia, anomalie scheletriche, bassa statura Sindrome/Orecchio, rotula, bassa statura Sindrome]•Ear, patella, short stature syndrome[EPS/Microtia, absent patellae, micrognathia syndrome/Meier-Gorlin Syndrome]•Meier gorlin syndrome de[Microtie squelette anomalies petite taille]••{224690}
* Meier Rotschild Sindrome di••Meier rotschild syndrome de••{}
* Meige Malattia di/Meigel Malattia diLinfoedema ereditario/Linfedema congenito ereditario/Malattia di Meige-Milroy/Trofoedema cronico primario/Elefantiasi nostras/Linfoedema primario/Pseudoelelefantiasi neuro-artritica di Nonne-Milroy/Linfedema congenito ereditario]•Congenital hereditary lymphoedema••Meige, Enfermedad de[Milroy, Enfermedad de/Linfedema Hereditario/Linfedema Primario]•{153100-153200-153400}
* Meige Sindrome di [Distonia Orofacciale/Malattia di Meig-Milroy/Malattia di Milroy/Malattia o Sindrome di Nonne-Milroy]•••Meige Syndrome•Meige, Síndrome de[Nonne Milroyb Meige, Síndrome de/Distonía Orofacial Bucal/Blefarospasmo Idiopático y Distonía Oromandibular, Síndrome del/Brueghel, Síndrome de/Distonía Craneal Segmentaria]•{}•A(Vedi =>Distonia)•S
* Meigel Malattia di••Meigel maladie de••{}
* Meinecke Sindrome di••Meinecke syndrome de[Pouces larges retard mental]••{}
* Meinecke Peper Sindrome di••Meinecke peper syndrome de[Dysplasie frontonasale phocomelie anomalies congenitales]••{}
* Melanoma CDKN24••••{600160}•D
* Melanoma familiare CDK4••Mélanome familial••{155600}•D
* Melanoma maligno•Melanoma,0 Malignant•••{}
* MELAS SINDROME/MELAS sindrome•MELAS Syndrome•MELAS syndrome•MELAS•{540000}•D
* Meleda Malattia di[Mal di Meleda/Cheratodermia di Meleda]•Meleda Disease[MDM/Keratosis Palmoplantaris Transgradiens of Siemens]•Mal de Meleda[Kératodermie de Meleda]•Meleda, Enfermedad de[Mal de Meleda]•{248300}
* Melhem Fahl Sindrome di••Melhem fahl syndrome de••{}
* MELKERSSON-ROSENTHAL SINDROME DI/Melkersson Rosenthal Sindrome di[Sindrome di Melkersson/Paralisi recidivanti del facciale ed edema del viso/Cheilite di Miescher/Cheilite granulomatosa/Sindrome del ganglio genicolato]•Melkersson Rosenthal Syndrome•Melkersson rosenthal syndrome de•Melkersson Rossenthal, Síndrome de[Síndrome de Melkersson]•{155900}
* Melnick-Fraser Sindrome di[Sindrome Bor/Sindrome branchio-oto-renale]••BOR syndrome•Melnick Fraser, Síndrome de•{}
* Melnick-Needles Sindrome di•Melnick Needles Syndrome•Melnick-Needles, syndrome de••{}
* Mende Sindrome di•••Mende, Síndrome de•{}
* Mendes da Costa Sindrome di[Eritrocheratodermia variabile]•Erythrokertodermia variabilis[EKV/Erythrokertodermia figurata, congenital familial, in plaques/Erythrokertodermia variabilis with erythema gyratum repens/Greither disease/Keratosis palmoplantaris transgrediens et progrediens]••Mendes da Costa, Síndrome de[Eritroqueratodermia Variable/Greither, Enfermedad de/Eritroqueratodermia Figurata/Transtorno de la Queratinización 18/Queratosis Rubra Figurata]•{133200}
* Menetrier Malattia di[Gastrite ipertrofica a pliche giganti/Gastropatia ipertrofica/Muco-adenomatosi gastrica/Gastrite pseudo-tumorale/Gastrite ipertrofica gigante]••Menetrier maladie de•Menetrier, Enfermedad de•{}
* Mengel Konigsmark Sindrome di••Mengel konigsmark sindrome de••{}
* Meniere Malattia di Sindrome di[Vertigine labirintica parossistica /Vertigine ricorrete con acufeni e sordità/Idrope endolinfatica labirintica/Vertigine auricolare/Vertigine aurale/Ipertensione idiopatica dell'endolinfa/Oticodinia]•Meniere Disease•••{}
* Meningioma•Meningioma•Meningiome••{}
* Meningite•Meningitis[Spinal arachnoiditis]••Meningitis Serosa Circunscrita[Aracnoiditis Espinal/Aracnoiditis Cerebral/Aracnoiditis Crónica Adhesiva]•{182950}
* Meningite meningococcica/Meningite da meningococci•Meningitis, Meningococcal[Bacterial Meningococcal Meningitis/Epidemic Cerebrospinal Meningitis/Meningococcal Meningitis]•••{-}

Meningite tubercolare•Meningitis, Tuberculous•••{}
* Meningiti batteriche•Meningitis, Bacterial••Meningitis Criptocócica[Meningitis Torular]/Meningitis por Listeria•{}
* Meningococcemia•Meningococcemia•••{}
* Menkes Sindromedi Malattia di/Menkes Sindrome di[Sindrome o malattia dei capelli attorcigliati/malattia dei capelli di acciaio]•Menkes Disease/Menkes syndrome/Menkes disease•Menkes, syndrome de•Menkes I, Síndrome de/Menkes, Enfermedad de/Menkes I, Síndrome de•{}
* Menkes-Kaplan Sindrome di•Menkes-Kaplan syndrome•••{}
* Menopausa precoce di origine genetica••Ménopause précoce d'origine génétique••{}
* Meretoja sindrome di••Meretoja syndrome de••{}
* Merlob Sindrome di••Merlob syndrome de••{}
* Merlob Grunebaum Reisner Sindrome di••Merlob grunebaum reisner syndrome de••{}
* MERRF SINDROME/MERRF SINDROME/MERRF sindrome•MERRF Syndrome•MERRF syndrome••{545000}•D
* Mehta Lewis Patton Sindrome di••Mehta lewis patton syndrome de••{}
* Meier Blumberg Imahorn Syndrome di••Meier blumberg imahorn syndrome de••{}
* Mesenterite Retrattile•Mesenteritis, Retractile[Mesenteric Panniculitis/Nodular Mesenteritis/Non-specific Sclerosing Mesenteritis/Sclerosing Panniculitis]••{}
* Metacondromatosi••Metachondromatose••{156250}
* Metalli pesanti Avvelenamento da••Heavy Metal Poisoning••{-}
* Meulengracht Malattia di Sindrome di[Ittero giovanile intermittente costituzionale/Sindrome di Gilbert Lereboullet]•••Meulengracht, Enfermedad de[Síndrome Gilbert Lereboullet]•{}
* Meyer-Schwinkerath and Weyers Sindrome di•Meyer-Schwinkerath and Weyers syndrome•••{}
* Meyer-Schwinkerath Sindrome di•Meyer-Schwinkerath syndrome••Meyer Schwickerath, Sindrome de•{}
* Mialgia eosinofila•Eosinophilia Myalgia•Myalgie eosinophilie liees au tryptophane••{}
* Miastenia acquisita••••{}
* Miastenia Gravis/Miastenia grave•Myasthenia Gravis•Myasthenia gravis[Myasthénie acquise]•Miastenia Gravis[M.G. Congénita /M. G.Generalizada/M. G. Infantil Familiar/M.G. Neonatal Transitoria/M.G.Pseudoparalítica]•{}
* Michelin Bebe Malattia del••••{}
* Michels Sindrome di•Michels syndrome•Michels syndrome de••{}
* Michels Caskey Sindrome di••Michels caskey syndrome de••{}
* Mickleson Sindrome di••Mickleson syndrome de••{}
* MICROANGIOPATIE TROMBOTICHE••Microangiopathie thrombotique familiale••{}
* MICROCEFALIA(//)

/Microcefalia

/Microcefalia albinismo anomalie digitali

/Microcefalia autosomica dominante

/Microcefalia brachidattilia cifoscoliosi

/Microcefalia calcificazioni intracraniche

/Microcefalia capelli radi ritardo mentale epilessia

/Microcefalia cardiomiopatia

/Microcefalia cardiopatia malsegmentazione polmonare

/Microcefalia displasia corio-retinica tipo recessivo

/Microcefalia fusione delle vertebre cervicali

/Microcefalia -immunodeficienza Malattia H4457linforeticolare

/Microcefalia ipogammaglobulinemia anomalie immunitarie

/Microcefalia ipogonadismo ipergonadotropico bassa statura

/Microcefalia ipoplasia cerebrale spasticità

/Microcefalia ipoplasia ponto-cerebellare discinesia

/Microcefalia linfedema corioretinite displasia

/Microcefalia linfedema Sindrome

/Microcefalia mesobrachifalangia fistola tracheo-esofagea

/Microcefalia microcornea sindrome tipo Seemanova

/Microcefalia microftalmia cecità

/Microcefalia micropene convulsioni

/Microcefalia ritardo mentale retinopatia

/Microcefalia ritardo mentale spasticità epilessia

/Microcefalia schisi labio-palatina polidattilia

/Microcefalia schisi palatina sindrome autosomica dominante

/Microcefalia sindrome nefrotica sclerosi mesangiale

/Microcefalia sordità

•microcephalic dwarfism

microcephalic primordial dwarfism 1

microcephalic primordial dwarfism-cataracts syndrome

microcephaly-calcification of cerebral white matter syndrome {251290}

microcephaly-cardiomyopathy syndrome

microcephaly-chorioretinopathy syndrome

microcephaly-deafness syndrome {156620}

microcephaly-digital anomalies syndrome

microcephaly-hiatus hernia-nephrotic syndrome

microcephaly-hypergonadotropic hypogonadism-short stature syndrome

microcephaly-infantile spasms-psychomotor retardation-nephrotic syndrome

microcephaly-mental retardation-cataract-hypogonadism syndrome

microcephaly-mental retardation-retinopathy syndrome

microcephaly-mesobrachyphalangy-tracheoesophageal fistula (MMT) syndrome

microcephaly-microphthalmia-ectrodactyly-prognathism (MMEP) syndrome

microcephaly-mild developmental delay-short stature-distinctive face syndrome

microcephaly-mild mental retardation-short stature-skeletal anomalies syndrome[microcephaly-cervical spine fusion anomalies] 251250

microcephaly-muscular build-rhizomelia-cataracts syndrome

microcephaly-oculo-digito-esophageal-duodenal (MODED) syndrome

microcephaly-sparse hair-mental retardation-seizures syndrome

microcephaly-spastic diplegia syndrome

•Microcephalie

Microcephalie albinisme anomalies digitales

Microcephalie autosomique dominant

Microcephalie brachydactylie cyphoscoliose

Microcephalie calcifications intracraniennes

Microcephalie cardiomyopathie[Winship viljoen leary syndrome de]

Microcephalie cardiopathie malsegmentation pulmonaire

Microcephalie cheveux rares retard mental epilepsie

Microcephalie dysplasie chorio retinienne type recessif

Microcephalie epilepsie retard mental cardiopathie

Microcephalie fente labiopalatine polydactylie

Microcephalie fente palatine syndrome autosomique dominant

Microcephalie fusions cervicales vertebrales

Microcephalie hypogammaglobulinemie immunite anormale

Microcephalie hypogonadisme hypergonadotropic petite taille

Microcephalie hypoplasie cerebrale spasticite

Microcephalie hypoplasie pontocerebelleuse dyskinesie

Microcephalie lymphoedeme chorioretine dysplasie

Microcephalie lymphoedeme syndrome

Microcephalie mesobrachyphalange fistule tracheo oesophagienne

Microcephalie microcornee syndrome type seemanova

Microcephalie micropenis convulsions

Microcephalie microphtalmie cecite

Microcephalie retard mental retinopathie

Microcephalie retard mental spasticite epilepsie

Microcephalie surdite

Microcephalie syndactylie brachymesophalangie

Microcephalie syndrome nephrotique sclerose mesangiale

Microcéphalie-immunodéficience-lymphoréticulome[Nijmegen breakage syndrome]

••{}
* Microcitemia=>Talassemie
* Microftalmia

/Microftalmia

/Microftalmia anomalie degli arti

/Microftalmia aplasia dermica sclerocornea

/Microftalmia camptodattilia ritardo mentale

/Microftalmia cataratta

/Microftalmia cisti colobomatose bilaterali rene policistico

/Microftalmia colobomatosi

/Microftalmia ernia diaframmatica Fallot

/Microftalmia microtia acinesia ritardo mentale

/Microftalmia ritardo mentale

/Microftalmia tipo Lenz

••••

{}
* Mielinolisi centrale diffusa••Myélinolyse centrale diffuse••{}
* Mielite•Myelitis•••{}
* Mielofibrosi idiopatica•Myelofibrosis, Idiopathic••Mielofibrosis Idiopática[Mielofibrosis Primaria /Mielofibrosis y Metaplasia Mieloide/Mielofibrosis y Osteosclerosis/Mieloesclerosis]•{}
* Mieloma multiplo[Malattia di Kahler]•Myeloma, Multiple•Myélome multiple•Mieloma Múltiple[Mieloma de Células Plasmáticas/Mielomatosis]•{254500}
* Mielomeningocele••Myéloméningocèle••{}
* Miescher 2 Sindrome di•Miescher syndrome 2•••{}
* Mietens Sindrome di•Mietens syndrome•Mietens syndrome de••{}
* Mietens-Weber Sindrome di•Mietens-Weber syndrome•••{}
* Mievis Verellen Dumounin Sindrome di••Mievis verellen dumounin syndrome de••{}
* Mikati Najjar Sahli Sindrome di••Mikati najjar sahli syndrome de••{}
* Mikulicz Sindrome di[Acroacitosi]•Mikulicz Syndrome•••{}
* Miles Sindrome di Malattia di•Miles syndrome•••{}
* Miles-Carpenter Sindrome di[MCS]•Miles-Carpenter syndrome (MCS)•••{}
* Miller Fisher Sindrome di[Polinevrite acuta idiopatica associata a oftalmoplegia/ Sindrome oftalmoplegia-atassia-areflessia/Sindrome di Fisher-Miller]••Miller fisher syndrome••{}
* Miller Sindrome di=>Disostosi acrofacciale postassiale
* Miller-Dieker Sindrome di•Miller-Dieker syndrome (MDS)/Miller-Dieker lissencephaly syndrome (MDLS)•Miller-Dieker, syndrome de••{247200}•D
* Milner Khallouf Gibson Sindrome di••Milner khallouf gibson syndrome••{}
* Milroy Malattia di =>Vedi Meige Malattia di
* Minkowski-Chauffard Malattia diSindrome di Gansslen/Malattia di Chauffard/Ittero emolitico congenito familiare/ Sferocitosi ereditaria/Ittero acolurico/Ittero familiare cronico]••Minkowski-Chauffard, maladie de••{}
* Minot Von Willebrand Malattia di•••Minot Von Willebrand, Enfermedad de[Willebrand Juergens, Enfermedad/Hemofilia Vascular/Pseudohemofilia/Von Willebrand, Enfermedad de/Trombopatía Constitucional/Angiohemofilia]•{}
* Minoxidil, esposizione prenatale al••••{-}
* Miocardiopatia mitocondriale••••{251900}•D
* MIOCLONO ESSENZIALE EREDITARIO•Myoclonus, General•••{159900}
* Miofibromatosi infantile•••Miofibromatosis•{}
* MIOPATIA CENTRAL CORE/Miopatia congenita 'central core'•Central Core Disease•Myopathie congénitale à cores centraux••{}
* MIOPATIA CENTRONUCLEARE[Miopatia miotubulare]/Miopatia congenita centronucleare•Central Core Disease of Muscle•Myopathie congénitale centronucléaire•Miopatía Centro Nuclear[Miopatía Congenita no Progresiva con Núcleo Central /Miopatía Fibrilar Central]•{117000}•M
* Miopatia scapulo-peronale•Myopathy, Scapuloperoneal•••{}
* MIOPATIE CONGENITE EREDITARIE

/Miopatia cardioscheletrica-neutropenia

/Miopatia cataratta ipogonadismo

/Miopatia con aggregati tubolari

/Miopatia con autofagia eccessiva

/Miopatia con sovraccarico lipidico

/Miopatia congenita con inclusioni citoplasmatiche

/Miopatia congenita multi-minicores
* /Miopatia da lisi delle miofibrille di tipo 1

/Miopatia da sovraccarico lipidico multisistemico

/Miopatia distale con debolezza delle corde vocali

/Miopatia distale di tipo Markesbery-Griggs

/Miopatia distale di tipo Nonaka

/Miopatia distale di tipo Welander, tipo svedese

/Miopatia distale (termine generico)

/Miopatia dominante benigna

/Miopatia e diabete melito

/Miopatia ereditaria con inclusioni filamentose intranucleari

/Miopatia miotonica prossimale (PROMM)

/Miopatia miotubulare congenita

/Miopatia mitocondriale acidosi lattica

/Miopatia mitocondriale anemia sideroblastica

/Miopatia mitocondriale cataratta

/Miopatia Moebius Robin Sindrome di

/Miopatia oftalmoplegia ipoacusia ariflessia

/Miopatia ritardo di crescita ritardo mentale ipospadia

/Miopatia siringomelia

/Miopatia tibiale di Udd

/Miopatia tipo Bethlem

/Miopatia tipo hutterita

/Miopatia tipo McArdle

/Miopatia vacuolare

/Miopatia viscerale familiare

/Miopatia viscerale familiare oftalmoplegia esterna

•myopathy-lactic acidosis-sideroblastic anemia syndrome

myopathy-myxedema syndrome

•Myopathie avec agregats tubulaires

Myopathie avec autophagie excessive

Myopathie avec surcharge en desmine

Myopathie avec surcharge lipidique

Myopathie cardiosquelettique-neutropénie

Myopathie cataracte hypogonadisme

Myopathie congénitale avec inclusions cytoplasmiques

Myopathie congénitale centronucléair

Myopathie congénitale à bâtonnets

Myopathie congénitale à cores centraux

Myopathie congénitale à multi-minicores

Myopathie distale

Myopathie distale avec faiblesse des cordes vocales

Myopathie distale de type Markesbery-Griggs

Myopathie distale de type Nonaka

Myopathie distale de type Welander, type suédois

Myopathie dominante bénigne

Myopathie et diabete sucre

Myopathie héréditaire à inclusions filamentaires intranucléaires

Myopathie mitochondriale acidose lactique

Myopathie mitochondriale anemie sideroblastique

Myopathie mitochondriale cataracte

Myopathie moebius robin syndrome

Myopathie myotonique proximale (PROMM)

Myopathie ophtalmoplegie hypoacousie areflexie

Myopathie par lyse des myofibrilles de type 1

Myopathie retard de croissance retard mental hypospadias

Myopathie syringomelie

Myopathie tibiale de Udd

Myopathie type Bethlem

Myopathie type hutterite

Myopathie type Mc Ardle

Myopathie viscerale familiale

Myopathie viscerale familiale ophtalmoplegie externe

Myopathie à corps cytoplasmiques

Myopathie à surcharge lipidique multisystémique

•Miopatía Centro Nuclear

Miopatía con Déficit de Carnitin Palmitoil Transferasa

Miopatía Congenita no Progresiva con Núcleo Central

Miopatía Congenita no Progresiva

Miopatía de los Bastones

Miopatía Farmacogénica

Miopatía Fibrilar Central

Miopatía Lipídica asociada con Déficit de SCAD

Miopatía Metabólica por Déficit de Carnitin Palmitoil Transferasa

Miopatía por Déficit de Carnitina

•{}
* Miopatia Congenita tipo Batten Turner•Myopathy, Congenital, Batten Turner Type•••{}
* Miopatia Congenita di Thomsen, autosomica••Myotonie congénitale de Thomsen••{160800}•D
* MIOPATIA DESMIN STORAGE/Miopatia con sovraccarico di desmina•Myopathy, Desmin Storage•••{}
* Miopatia miotubulare congenita•Myopathy, Myotubular•Myopathie congénitale myotubulaire• Miopatía Miotubular •{310400}•D
* MIOPATIA NEMALINICA/Miopatia nemalinica•Nemaline Myopathy[Congenital Rod Disease/NM/Rod Myopathy]•Myopathie némaline•Miopatía Nemalínica•{256030}•D
* MIOPATIA MITOCONDRIALE- ENCEFALOPATIA- ACIDOSI LATTICA-ICTUS/Miopatia mitocondriale-encefalopatia-acidosi lattica••Myopathie mitochondriale-encéphalopathie-acidose lactique•Miopatía, Encefalopatía Mitocondrial, Acidosis Láctica y Episodios Stroke Like•{540000}
* Miopia infantile grave••Myopie infantile forte••{255500}
* Miopia grave[Miopia alto grado autosomica dominante]•Myopia, high-grade, autosomal dominant 1[Myopia 2/MYP2]•Myopie sévère••{160700}
* Miosite ossificante progressiva••Myosite ossifiante progressive•Miositis Osificante Progresiva•{}
* Miotonia ritardo mentale anomalie scheletriche••Myotonie retard mental anomalies squelettiques••{}
* Miotonia condrodistrofica•myotonia chondrodystrophica•Myotonie chondrodystrophique••{}
* Miotonia congenita di Becker/Miotonia congenita di Thomsen•Myotonia Congenita•Myotonie congénitale de Becker••{}
* Mirhosseini Holmes Walton Sindrome di•Mirhosseini-Holmes-Walton syndrome•Mirhosseini holmes walton syndrome••{}
* Mitchell Malattia di•••Mitchell, Enfermedad de[Eritromelalgia/Eritermalgia/Weir Mitchell, Enfermedad de/Gerhardt, Enfermedad de]•{}
* Mitocondriali Malattie[Citopatie mitocondriali (termine generico)]

••Maladies mitochondriales (terme générique)

Maladies mitochondriales d origine nucleaire

Maladies mitochondriales, cliniquement non définies

••{}
* Miura Sindrome di••Miura syndrome de••{}
* Mixoma atriale••Myxome auriculaire••{}
* Mixoma-iperpigmentazione-iperattività endocrina••Myxome-hyperpigmentation-hyperactivité endocrinienne••{}
* MOEBIUS SINDROME DI/MOEBIUS SINDROME DI/Moebius Sindrome di[Paralisi congenita del VI e del VII/ Paralisi oculofacciale congenita/ agenesia o aplasia nucleare congenita/Diplegia Facciale Congenita/ Paralisi congenita abducente-facciale/Sindrome di Von Graefe]•Moebius Syndrome/MBS1[FACIAL DIPLEGIA, CONGENITAL]/MBS2/MBS3•Moebius, syndrome de•Moebius, Síndrome de•{157900-601471-604185}•A•S
* Moerman Vandenberghe Fryns Sindrome di••Moerman vandenberghe fryns syndrome••{}
* Moeschler Claren Sindrome di••Moeschler claren syndrome de••{}
* Molari piramidali glaucoma anomalia del labbro superiore••••{}
* Mohr Sindrome di[Sindrome OFD tipo II]•Mohr syndrome•Mohr syndrome de••{}
* Mohr-Claussen Sindrome di•Mohr-Claussen syndrome•••{}
* Mohr-Tranebjaerg Sindrome di[MTS]•Mohr-Tranebjaerg syndrome (MTS)•••{}
* Moloney sindrome di••Moloney syndrome de••{}
* Mollica syndrome•Mollica syndrome•••{}
* Mollica Pavone Antener Sindrome di•Mollica-Pavone-Anterer syndrome•Mollica pavone antener syndrome de••{}
* Mongolismo=>Sindrome di Down
* Mononen Karnes senac Sindrome di••Mononen karnes senac syndrome••{}
* Monosomia[delezione]=>Vedi Cromosoma(//)
* Montagna forma acuta Mal di[ipobaropatia]••Mountain Sickness, Acute••{}
* Montefiore Sindrome di•Montefiore syndrome•Montefiore syndrome de••{}
* Moore Federman Sindrome di••Moore federman syndrome de••{}
* Moore Smith Weaver Sindrome di••Moore smith weaver syndrome de••{}
* Moore Weaver Sindrome di••Moore weaver syndrome de••{}
* Morbillo•Measles[Morbilli/Nine Day Measles/Rubeola]•••{-}
* Moreno Zachai Kaufman Sindrome di••Moreno zachai kaufman syndrome de••{}
* Morgagni Stewart Morel Sindrome di[Iperostosi frontale interna/Endocraniosi iperostosica di Morgagni/Sindrome di Morgagni-Morel/Sindrome di Stewart-Morel/Craniopatia metabolica]•••Morgagni Stewart Morel, Síndrome de•{}
* Morgagni-Turner Sindrome di•Morgagni-Turner syndrome•••{}
* Morgagni Turner Albright Sindrome di•Morgagni-Turner-Albright syndrome••Morgagni Turner Albright, Síndrome de•{}
* Morillo Cucci Passarge Sindrome di••Morillo cucci passarge syndrome de••{}
* MORQUIO MALATTIA DI/Morquio Malattia di[Mucopolisaccaridosi tipo IV/Condrodistrofia ereditaria /Condrodisplasia spondiloepifisaria/Cheratosulfaturia/Condrodistrofia tarda/Condrodistrofia atipica/Sindrome di Morquio-Ullrich/Sindrome di Brailsford]•Morquio Syndrome/Morquio syndrome or disease•Morquio, maladie de[Mucopolysaccharidosetype 4]•Morquio, Enfermedad de•{}
* Morquio-Brailsford Sindrome di Malattia di•Morquio-Brailsford syndrome or disease•••{}
* Morquio-Ullrich Sindrome di Malattia di•Morquio-Ullrich syndrome or disease[mucopolysaccharidosis(MPS) IV (A, B)]•••{}
* Morrison Young Sindrome di••Morrison young syndrome de••{}
* Morse Rawnsley Sargent Sindrome di••Morse rawnsley sargent syndrome de••{}
* MORNING GLORY ANOMALIA DI••••{120330}
* Morte neonatale deficit immunitario/Morte improvvisa del lattante••Mort neonatale deficit immunitaire[Woods black norbury syndrome de]/Sudden Infant Death Syndrome••Muerte Súbita Infantil•{}
* Morte nera=>Peste
* MOSCHOWITZ SINDROME DI[PORPORA TROMBOTICA TROMBOCITOPENICA/Trombosi piastrinica disseminata arteriolare-capillare/ Anemia emolitica trombotica microangiopatica/Sindrome trombotica piastrinica/Acroangiomatosi trombocitica/Trombosi piastrinica disseminata arteriolare-capillare/Anemia emolitica trombotica microangiopatica/Sindrome di Moschowitz-Singer-Symmers]•Purpura, Thrombotic Thrombocytopenic••Moschowitz, Enfermedad de•{}
* Mounier-Kuhn Sindrome di[Tracheobroncomegalia/Tracheobroncopatia malacica bronchiectasica/Megatrachea idiopatica con tracheomalacia e tracheo broncoectasie/Sindrome sinusite-bronchiectasie]••Mounier-Kuhn, syndrome de••{}
* Mount Reback Sindrome diCoreoatetosi parossistica familiare]•Paroxysmal nonkinesigenic dyskinesia[PNKD/Paroxysmal dystonic choreoathetosis/PDC/Choreoathetosis, Familial Paroxysmal/FPD1/Mount Reback Sy ndrome/Choreoathetosis, nonkinesigenic/Dystonia 8/DYT8]•Mount reback syndrome[Choreoathetose paroxystique familiale]••{118800}
* Mousa Al Din Al Nassar Sindrome di[Degenerazione spinocerebellare con distrofia maculo-corneale, cataratta congenita, e miopia]•Bedouin spastic ataxia Syndrome[Spinocerebellar degeneratione with macular corneal dystrophy, congenital cataracts, and myopia]•Mousa al din al nassar syndrome d••{271320}
* Moyamoya Malattia di[Moya-Moya Malattia di/Malattia di Nishimoto]•Moyamoya Disease•Moya-Moya, maladie de•Moya Moya, Enfermedad de[Nishimoto, Enfermedad de]•{252350}•M
* Moynahan Sindrome di•Moynahan syndrome 1/Moynahan alopecia syndrome•Moynahan syndrome de••{}
* Mucha Habermann Malattia di[Pitiriasi lichenoide varioliforme acuta /Malattia di Habermann/Malattia di Mucha/Malattia di Wise/Parapsoriasi varioliforme/Pitiriasi lichenoisd e varioliforme acuta]•Mucha Habermann Disease••Mucha Habermann, Enfermedad de[Parapsoriasis en Gotas/Parapsoriasis Guttata/Pitiriasis Liquenoide y Varioliforme Aguda]•{}
* Muckle-Wells Sindrome di/Sindrome di Muckle-Wells[MWS]••Muckle-Wells, syndrome de••{}
* MUCOLIPIDOSI[ML]•Mucolipidosis IV•Mucolipidose type 1 /type 2 /type 3 /type 4•Mucolipidosis Tipo I/Mucolipidosis Tipo IV•{-252650}
* MUCOPOLISACCARIDOSI[MPS]

/Mucopolisaccaridosi tipo 1

/Mucopolisaccaridosi tipo 2

/Mucopolisaccaridosi tipo 3

/Mucopolisaccaridosi tipo 4

/Mucopolisaccaridosi tipo 6

/Mucopolisaccaridosi tipo 7

•Mucopolysaccharidosis

mucopolysaccharidosis (MPS) I

mucopolysaccharidosis (MPS) II

mucopolysaccharidosis (MPS) III (A, B, C, D)

mucopolysaccharidosis (MPS) IV (A, B)

mucopolysaccharidosis (MPS) VI

mucopolysaccharidosis (MPS) VII

mucopolysaccharidosis (MPS) VIII

mucopolysaccharidosis F

•Mucopolysaccharidose type 1

Mucopolysaccharidose type 2

Mucopolysaccharidose type 3

Mucopolysaccharidose type 4

Mucopolysaccharidose type 6

Mucopolysaccharidose type 7

•Mucopolisacaridosis Tipo I

Mucopolisacaridosis Tipo II

Mucopolisacaridosis Tipo III

Mucopolisacaridosis IV

Mucopolisacaridosis Tipo VI

Mucopolisacaridosis Tipo VII

•{252700-309900-252900}•D•A•S
* Mucoviscidosi=>Fibrosi Cistica
* Muir-Torre Sindrome di••Muir-Torre, syndrome de••{}
* Muller Sindrome[Sindrome Sturge-Weber/SBS/Angioma capillare e venoso calcificante/angiomatosi encefalofacciale/Amgiomatosi cerebrocutanea/Angiomatosi meningofacciale]•Müller syndrome[Sturge-Weber syndrome/SWS/Dimitri disease/Jahnke syndrome/Kalischer syndrome/Lawford syndrome/Parkes Weber syndrome/Parkes Weber and Dimitri syndrome/Schirmer syndrome/Sturge disease/Sturge syndrome/Sturge-Kalischer-Weber syndrome/Sturge-Weber angiomatosis/Sturge-Weber anomalad/Sturge-Weber-Dimitri syndrome/Sturge-Weber-Krabbe syndrome/Sturge-Weber-Thoma syndrome/Weber syndrome/Weber-Dimitri syndrome/angioma capillare et venosum calcificans/angiomatosis encephalofacialis/angiomatosis meningoulofacialis/angiomatosis-oculo-orbito-thalamo-encephalic syndrome/cerebrocutaneous angiomatosis/cutaneocerebral angioma/ectoneurodermal hamartoma/encephalocraniofacial angiomatosis/encephalofacial angiomatosis/encephalofacial neuroangiomatosis/encephalotrigeminal angiomatosis/encephalotrigeminal syndrome/fourth phacomatosis/meningeal capillary angiomatosis/meningofacial angiomatosis/meningo-oculofacial angiomatosis/neuroangiomatosis encephalofacialis/neurocutaneous syndrome/neuroectodermal hamartoma/neuro-oculocutaneous angiomatosis/neuroretinoangiomatosis/nevoid amentia/trigemino-encephalo-angiomatosis]•••{185300}
* Muller Barth Menger Sindrome di[Malformazioni cerebrali, ipertricosi, camptodattilia]•Cerebral malformation, seizures, hypertrichosis, and overlapping fingers•Muller barth menger syndrome de[Malformations cerebrales hypertrichose camptodactylie]••{213820}
* Mulliez Roux Loterman Sindrome di••Mulliez roux loterman syndrome de••{}
* Mulvihill Smith Sindrome di•Mulvihill Smith Syndrome/Mulvihill-Smith syndrome•Mulvihill smith syndrome de••{}
* MURCS associazione•MURCS Association•Murcs association•