List of diseases (M)

A list of diseases.

Diseases
Alphabetical list
0–9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
See also
Health Exercise Nutrition

Ma • Mc • Me • Mi • Ml–Mn • Mo • Mp–Mt • Mu • My

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Ma

Mac • Mad–Mak • Mal • Man • Mar • Mas–May

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Mac

• Mac Dermot Patton Williams syndrome
• Mac Dermot Winter syndrome

Maci–Macr

• Macias–Flores–Garcia–Cruz–Rivera syndrome
• Mackay–Shek–Carr syndrome
• Macleod–Fraser syndrome
• Macrocephaly cutis marmorata telangiectatica
• Macrocephaly dominant type
• Macrocephaly mental retardation facial dysmorphism
• Macrocephaly mesodermal hamartoma spectrum
• Macrocephaly mesomelic arms talipes
• Macrocephaly pigmentation large hands feet
• Macrocephaly short stature paraplegia
• Macrodactyly of the foot
• Macrodactyly of the hand
• Macroepiphyseal dysplasia Mcalister Coe type
• Macroglobulinemia
• Macroglossia dominant
• Macroglossia exomphalos gigantism
• Macrogyria pseudobulbar palsy
• Macrophagic myofasciitis
• Macrosomia developmental delay dysmorphism
• Macrosomia microphthalmia cleft palate
• Macrothrombocytopenia progressive deafness
• Macrothrombocytopenia with leukocyte inclusions

Macu

• Macular corneal dystrophy
• Macular degeneration
  • Macular degeneration juvenile
  • Macular degeneration, age-related
  • Macular degeneration, polymorphic
• Macular dystrophy, vitelliform
• Macules hereditary congenital hypopigmented and hyperpigmented

Mad–Mak

• Mad cow disease
• Madelung's disease
• Madokoro–Ohdo–Sonoda syndrome
• Maffucci syndrome
• Maghazaji syndrome
• Magnesium defect in renal tubular transport of
• Magnesium wasting renal
• Major depressive disorder

Mal

• Mal de debarquement

Mala–Mall

• Malakoplakia
• Malaria
• Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase deficiency
• Male pseudohermaphroditism due to 5-alpha-reductase 2 deficiency
• Male pseudohermaphroditism due to defective LH molecule
• Malformations in neuronal migration
• Malignant astrocytoma
• Malignant fibrous histiocytoma
• Malignant germ cell tumor
• Malignant hyperthermia arthrogryposis torticollis
• Malignant hyperthermia

• Malignant hyperthermia susceptibility type 1
• Malignant hyperthermia susceptibility type 2
• Malignant hyperthermia susceptibility type 3
• Malignant hyperthermia susceptibility type 4
• Malignant hyperthermia susceptibility type 5
• Malignant hyperthermia susceptibility type 6

• Malignant mesenchymal tumor
• Malignant mixed Müllerian tumor
• Malignant paroxysmal ventricular tachycardia
• Mallory–Weiss syndrome

Malo–Malp

• Malonic aciduria
• Malonyl-CoA decarboxylase deficiency
• Malouf syndrome
• Malpuech facial clefting syndrome

Man

• Mandibuloacral dysplasia
• Mandibulofacial dysostosis deafness postaxial polydactyly
• Manic Depression, Bipolar
• Manic-depressive psychosis, genetic types
• Mannosidosis
• Manouvrier syndrome
• Mansonelliasis
• Mantle cell lymphoma

Mar

Mara–Marg

• Marashi–Gorlin syndrome
• Marburg fever
• Marchiafava–Bignami disease
• Marchiafava–Micheli disease
• Marcus Gunn phenomenon
• Marden–Walker-like syndrome
• Marden–Walker syndrome
• Marek disease
• Marfan syndrome
  • Marfan Syndrome type II
  • Marfan Syndrome type III
  • Marfan Syndrome type IV
  • Marfan Syndrome type V
• Marfan-like syndrome, Boileau type
• Marfan-like syndrome
• Marfanoid craniosynostosis syndrome
• Marfanoid hypermobility
• Marfanoid mental retardation syndrome autosomal
• Marginal glioneuronal heterotopia

Mari–Mart

• Marie type ataxia
• Marie–Unna congenital hypotrichosis
• Marinesco–Sjögren like syndrome
• Marinesco–Sjögren syndrome
• Marion–Mayers syndrome
• Markel–Vikkula–Mulliken syndrome
• Marles–Greenberg–Persaud syndrome
• Maroteaux–Cohen–Solal–Bonaventure syndrome
• Maroteaux–Fonfria syndrome
• Maroteaux–Le Merrer–Bensahel syndrome
• Maroteaux–Stanescu–Cousin syndrome
• Maroteaux–Verloes–Stanescu syndrome
• Maroteaux–Lamy syndrome
• Marphanoid syndrome type De Silva
• Marsden–Nyhan–Sakati syndrome
• Marsden syndrome
• Marshall syndrome
• Marshall–Smith syndrome
• Martinez–Monasterio–Pinheiro syndrome
• Martsolf–Reed–Hunter syndrome
• Martsolf syndrome

Mas–May

• MASA syndrome
• Mass psychogenic illness
• MASS syndrome
• Massa–Casaer–Ceulemans syndrome
• Mast cell disease
• Mastocytosis, short stature, hearing loss
• Mastocytosis
• Mastoiditis
• Mastroiacovo–De Rosa–Satta syndrome
• Mastroiacovo–Gambi–Segni syndrome
• MAT deficiency
• Maternal hyperphenylalaninemia
• Maternally inherited diabetes and deafness
• Mathieu–De Broca–Bony syndrome
• Matsoukas–Liarikos–Giannika syndrome
• Matthew–Wood syndrome
• Maturity onset diabetes of the young
• Maumenee syndrome
• Maxillary double lip
• Maxillofacial dysostosis
• Maxillonasal dysplasia, Binder type
• Mayer–Rokitanski–Kuster syndrome
• May–Hegglin anomaly

Mc

• McAlister–Crane syndrome
• McArdle disease
• McCallum–Macadam–Johnston syndrome
• McCune–Albright syndrome
• McDonough syndrome
• McDowall syndrome
• McGillivray syndrome
• McKusick–Kaufman syndrome
• McKusick type metaphyseal chondrodysplasia
• McLain–Debakian syndrome
• McPherson–Clemens syndrome
• McPherson–Robertson–Cammarano syndrome

Me

Mea–Med • Meg–Mei • Mel–Mem • Men • Mer–Mes • Met • Mev–Mey

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Mea–Med

• Meacham–Winn–Culler syndrome
• Meadows syndrome
• Measles
• Meckel like syndrome
• Meckel syndrome
• Medeira Dennis Donnai syndrome
• Median cleft lip corpus callosum lipoma skin polyps
• Median nodule of the upper lip
• Mediastinal endodermal sinus tumors
• Mediastinal syndrome
• Mediterranean fever
• Medium-chain Acyl-CoA dehydrogenase deficiency
• Medrano Roldan syndrome
• Medullary cystic disease
• Medullary thyroid carcinoma
• Medulloblastoma

Meg–Mei

• Megacystis microcolon intestinal hypoperistalsis syndrome
• Megaduodenum
• Mega-epiphyseal dwarfism
• Megalencephalic leukodystrophy
• Megalencephaly-cystic leukodystrophy
• Megaloblastic anemia
• Megalocornea mental retardation syndrome
• Megalocytic interstitial nephritis
• Mehes syndrome
• Mehta–Lewis–Patton syndrome
• Meier–Blumberg–Imahorn syndrome
• Meier–Rotschild syndrome
• Meige syndrome
• Meigel disease
• Meinecke–Pepper syndrome
• Meinecke syndrome

Mel–Mem

• Melanoma type 1
• Melanoma type 2
• Melanoma, familial
• Melanoma, malignant
• Melanoma-astrocytoma syndrome
• Melanosis neurocutaneous
• MELAS
• Meleda disease
• Melhem–Fahl syndrome
• Melioidosis
• Melkersson–Rosenthal syndrome
• Melnick–Needles osteodysplasty
• Melnick–Needles syndrome
• Membranoproliferative glomerulonephritis (type II)

Men

Mend–Meno

• Mendelian susceptibility to atypical mycobacteria
• Menetrier's disease
• Mengel–Konigsmark syndrome
• Ménière's disease
• Meningeal angiomatosis cleft hypoplastic left heart
• Meningioma 1
• Meningioma
• Meningitis, meningococcal
• Meningitis
• Meningocele
• Meningococcemia
• Meningoencephalocele
• Meningoencephalocele-arthrogryposis-hypoplastic thumb
• Meningomyelocele

Ment

Menta

Mental

Mental d – Mental m

• Mental deficiency-epilepsy-endocrine disorders
• Mental mixed retardation deafnes clubbed digits

Mental r

• Mental retardation

Mental retardation a – Mental retardation m

• Mental retardation anophthalmia craniosynostosis
• Mental retardation arachnodactyly hypotonia telangiectasia
• Mental retardation athetosis microphthalmia
• Mental retardation blepharophimosis obesity web neck
• Mental retardation Buenos Aires type
• Mental retardation cataracts calcified pinnae myopathy
• Mental retardation coloboma slimness
• Mental retardation contractural arachnodactyly
• Mental retardation dysmorphism hypogonadism diabetes
• Mental retardation epilepsy bulbous nose
• Mental retardation epilepsy
• Mental retardation gynecomastia obesity X linked
• Mental retardation hip luxation G6PD variant
• Mental retardation hypocupremia hypobetalipoproteinemia
• Mental retardation hypotonia skin hyperpigmentation
• Mental retardation macrocephaly coarse facies hypotonia
• Mental retardation microcephaly phalangeal facial
• Mental retardation microcephaly unusual facies
• Mental retardation Mietens–Weber type
• Mental retardation multiple nevi
• Mental retardation myopathy short stature endocrine defect
• Mental retardation nasal hypoplasia obesity genital hypoplasia

Mental retardation n – Mental retardation s

• Mental retardation nasal papillomata
• Mental retardation osteosclerosis
• Mental retardation progressive spasticity
• Mental retardation psychosis macroorchidism
• Mental retardation short broad thumbs
• Mental retardation short stature absent phalanges
• Mental retardation short stature Bombay phenotype
• Mental retardation short stature cleft palate unusual facies
• Mental retardation short stature deafness genital
• Mental retardation short stature hand contractures genital anomalies
• Mental retardation short stature heart and skeletal anomalies
• Mental retardation short stature hypertelorism
• Mental retardation short stature microcephaly eye
• Mental retardation short stature ocular and articular anomalies
• Mental retardation short stature scoliosis
• Mental retardation short stature unusual facies
• Mental retardation short stature wedge shaped epiphyses
• Mental retardation skeletal dysplasia abducens palsy
• Mental retardation Smith–Fineman–Myers type
• Mental retardation spasticity ectrodactyly

Mental retardation u – Mental retardation x

• Mental retardation unusual facies Ampola type
• Mental retardation unusual facies Davis–Lafer type
• Mental retardation unusual facies talipes hand anomalies
• Mental retardation unusual facies
• Mental retardation Wolff type
• Mental retardation X linked Atkin type
• Mental retardation X linked borderline Maoa metabolism anomaly
• Mental retardation X linked Brunner type
• Mental retardation X linked dysmorphism
• Mental retardation X linked dystonia dysarthria
• Mental retardation X linked severe Gustavson type
• Mental retardation X linked short stature obesity
• Mental retardation X linked Tranebjaerg type seizures psoriasis
• Mental retardation, unexplained
• Mental retardation, X linked, Marfanoid habitus
• Mental retardation, X linked, nonspecific
• Mental retardation, X-linked 14
• Mental retardation-polydactyly-uncombable hair

Mer–Mes

• Mercury poisoning (Mercurialism)
• Meretoja syndrome
• Merkle tumors
• Merlob–Grunebaum–Reisner syndrome
• Merlob syndrome
• Mesangial sclerosis, diffuse
• Mesenteric ischemia
• Mesenteric panniculitis
• Mesodermal defects lower type
• Mesomelia synostoses
• Mesomelia
• Mesomelic dwarfism cleft palate camptodactyly
• Mesomelic dwarfism Langer type
• Mesomelic dwarfism Nievergelt type
• Mesomelic dwarfism Reinhardt–Pfeiffer type
• Mesomelic dysplasia skin dimples
• Mesomelic dysplasia Thai type
• Mesomelic syndrome Pfeiffer type
• Mesothelioma

Met

Meta

• Metabolic acidosis
• Metabolic disorder
• Metabolic syndrome X
• Metacarpals 4 and 5 fusion
• Metachondromatosis
• Metageria
• Metaphyseal anadysplasia
• Metaphyseal chondrodysplasia Schmid type
• Metaphyseal chondrodysplasia Spahr type
• Metaphyseal chondrodysplasia, others
• Metaphyseal dysostosis mental retardation conductive deafness
• Metaphyseal dysplasia maxillary hypoplasia brachydactyly
• Metaphyseal dysplasia Pyle type
• Metastatic insulinoma
• Metatarsus adductus
• Metatrophic dysplasia
• Metatropic dwarfism

Meth

• Methimazole antenatal infection
• Methionine adenosyltransferase deficiency
• Methyl mercury antenatal infection
• Methylcobalamin deficiency cbl G type
• Methylcobalamin deficiency, cbl E complementation type
• Methylenetetrahydrofolate reductase deficiency
• Methylmalonic acidemia with homocystinuria
• Methylmalonic acidemia
• Methylmalonic aciduria microcephaly cataract
• Methylmalonicacidemia with homocystinuria, cbl D
• Methylmalonicaciduria with homocystinuria, cbl F
• Methylmalonicaciduria, vitamin B12 unresponsive, mut-0
• Methylmalonyl-Coenzyme A mutase deficiency

Mev–Mey

• Mevalonate kinase deficiency
• Mevalonicaciduria
• Meyenburg–Altherr–Uehlinger syndrome

Mi

Mib • Mic • Mid–Mir • Mis–Mix

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Mib

• Mibies syndrome

Mic

Mich–Mick

• Michelin tire baby syndrome
• Michels Caskey syndrome
• Michels syndrome
• Mickleson syndrome

Micr

Mircre

• Micrencephaly corpus callosum agenesis
• Micrencephaly olivopontocerebellar hypoplasia

Micro

• Micro syndrome

Microb

• Microbrachycephaly ptosis cleft lip

Microc

Microcephalic

• Microcephalic osteodysplastic primordial dwarfism
• Microcephalic primordial dwarfism Toriello type
• Microcephalic primordial dwarfism

Microcephaly

• Microcephaly

Microcephaly a – Microcephaly l

• Microcephaly albinism digital anomalies syndrome
• Microcephaly autosomal dominant
• Microcephaly brachydactyly kyphoscoliosis
• Microcephaly brain defect spasticity hypernatremia
• Microcephaly cardiac defect lung malsegmentation
• Microcephaly cardiomyopathy
• Microcephaly cervical spine fusion anomalies
• Microcephaly chorioretinopathy recessive form
• Microcephaly cleft palate autosomal dominant
• Microcephaly deafness syndrome
• Microcephaly developmental delay pancytopenia
• Microcephaly facial clefting preaxial polydactyly
• Microcephaly glomerulonephritis Marfanoid habitus
• Microcephaly hiatus hernia nephrotic syndrome
• Microcephaly hypergonadotropic hypogonadism short stature
• Microcephaly immunodeficiency lymphoreticuloma
• Microcephaly intracranial calcification
• Microcephaly lymphoedema chorioretinal dysplasia
• Microcephaly lymphoedema syndrome

Microcephaly m – Microcephaly w

• Microcephaly mental retardation retinopathy
• Microcephaly mental retardation spasticity epilepsy
• Microcephaly mesobrachyphalangy tracheoesophageal fistula syndrome
• Microcephaly microcornea syndrome Seemanova type
• Microcephaly micropenis convulsions
• Microcephaly microphthalmos blindness
• Microcephaly nonsyndromal
• Microcephaly pontocerebellar hypoplasia dyskinesia
• Microcephaly seizures mental retardation heart disorders
• Microcephaly sparse hair mental retardation seizures
• Microcephaly syndactyly brachymesophalangy
• Microcephaly with chorioretinopathy, autosomal dominant form
• Microcephaly with normal intelligence, immunodeficiency
• Microcephaly with spastic q­riplegia
• Microcephaly, holoprosencephaly, and intrauterine growth retardation
• Microcephaly, primary autosomal recessive

Microco

• Microcoria, congenital
• Microcornea correctopia macular hypoplasia
• Microcornea glaucoma absent frontal sinuses

Microd – Microv

• Microdontia hypodontia short stature
• Microencephaly
• Microgastria limb reduction defect
• Microgastria short stature diabetes
• Microinfarct
• Micromelic dwarfism Fryns type
• Micromelic dysplasia dislocation of radius
• Microphtalmos bilateral colobomatous orbital cyst
• Microphthalmia
• Microphthalmia, Lentz type
• Microphthalmia camptodactyly mental retardation
• Microphthalmia cataract
• Microphthalmia diaphragmatic hernia Fallot
• Microphthalmia mental deficiency
• Microphthalmia microtia fetal akinesia
• Microphthalmia with limb anomalies
• Microphthalmos, microcornea, and sclerocornea
• Microscopic polyangiitis

• Microsomia hemifacial radial defects
• Microspherophakia metaphyseal dysplasia
• Microsporidiosis
• Microtia, meatal atresia and conductive deafness
• Microvillus inclusion disease

Micu

• Miculicz syndrome

Mid–Mir

• MIDAS syndrome
• Midline cleft of lower lip
• Midline defects autosomal type
• Midline defects recessive type
• Midline developmental field defects
• Midline field defects
• Midline lethal granuloma
• Mietens syndrome
• Mievis–Verellen–Dumoulin syndrome
• Migraine
• Mikulicz syndrome
• Mild cognitive impairment
• Miller Fisher syndrome
• Miller–Dieker syndrome
• Milner–Khallouf–Gibson syndrome
• MILS syndrome
• Minamata disease
• Minkowski–Chauffard syndrome
• Minoxidil antenatal infection
• Miosis, congenital
• Mirhosseini–Holmes–Walton syndrome
• Mirror hands feet nasal defects
• Mirror polydactyly segmentation and limbs defects

Mis–Mix

• Mitochondrial cytopathy (generic term)
• Mitochondrial diseases of nuclear origin
• Mitochondrial diseases, clinically undefinite
• Mitochondrial disease
• Mitochondrial encephalomyopathy aminoacidopathy
• Mitochondrial genetic disorders
• Mitochondrial myopathy lactic acidosis
• Mitochondrial myopathy-encephalopathy-lactic acidosis
• Mitochondrial PEPCK deficiency
• Mitochondrial trifunctional protein deficiency
• Mitral atresia
• Mitral regurgitation deafness skeletal anomalies
• Mitral valve prolapse, familial, autosomal dominant
• Mitral valve prolapse, familial, X linked
• Mitral valve prolapse
• Miura syndrome
• Mixed connective tissue disease
• Mixed Müllerian tumor
• Mixed receptive-expressive language disorder
• Mixed sclerosing bone dystrophy

Ml–Mn

• MLS syndrome
• MMEP syndrome
• MMT syndrome
• MN1
• MNGIE syndrome

Mo

Mob–Mom • Mon–Moo • Mor–Moy

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Mob–Mom

• Möbius syndrome
• MODY syndrome
• Möbius axonal neuropathy hypogonadism
• Moerman Van den berghe Fryns syndrome
• Moeschler–Clarren syndrome
• Mohr syndrome
• Mohr–Tranebjærg syndrome
• Mollica–Pavone–Antener syndrome
• Molluscum contagiosum
• Moloney syndrome
• Molybdenum cofactor deficiency
• MOMO syndrome

Mon–Moo

• Mondini dysplasia
• Mondor's disease
• Monge's disease
• Monilethrix
• Monoamine oxidase A deficiency
• Monoclonal gammopathy of undetermined significance
• Monodactyly tetramelic
• Mononen–Karnes–Senac syndrome
• Mononeuritis multiplex
• Monosomy 8q12 21
• Monosomy 8q21 q22
• Monosomy X
• Montefiore syndrome
• Moore–Federman syndrome
• Moore–Smith–Weaver syndrome

Mor–Moy

• Morel's ear
• Moreno–Zachai–Kaufman syndrome
• Morgani–Turner–Albright syndrome
• Morgellons disease
• Morillo–Cucci–Passarge syndrome
• Morphea scleroderma
• Morphea, generalized
• Morquio disease, type A
• Morquio disease, type B
• Morquio syndrome
• Morrison–Young syndrome
• Morse–Rawnsley–Sargent syndrome
• Motor neuron disease
• Motor neuro-ophthalmic disorders
• Motor neuropathy peripheral dysautonomia
• Motor neuropathy
• Motor sensory neuropathy type 1 aplasia cutis congenita
• Mounier-Kuhn syndrome
• Mount–Reback syndrome
• Mousa Al din Al Nassar syndrome
• Moyamoya disease

Mp–Mt

• MPO deficiency
• MPS III-A
• MPS III-B
• MPS III-C
• MPS III-D
• MPS VI
• MRKH Syndrome (Müllerian agenesis)
• MSBD syndrome
• MTHFR deficiency

Mu

Muc–Mue • Mul • Mum–Mut

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Muc–Mue

• Mucha–Habermann disease
• Muckle–Wells syndrome
• Mucoepithelial dysplasia
• Mucolipidosis type 1
• Mucolipidosis type 3
• Mucolipidosis type 4
• Mucopolysaccharidosis type 3
• Mucopolysaccharidosis type 4
• Mucopolysaccharidosis type I Hurler syndrome
• Mucopolysaccharidosis type I Hurler/Scheie syndrome
• Mucopolysaccharidosis type I Scheie syndrome
• Mucopolysaccharidosis type II Hunter syndrome- mild form
• Mucopolysaccharidosis type II Hunter syndrome- severe form
• Mucopolysaccharidosis type IV-A Morquio syndrome
• Mucopolysaccharidosis type IV-B
• Mucopolysaccharidosis type V
• Mucopolysaccharidosis type VI Maroteaux-Lamy - severe, intermediate
• Mucopolysaccharidosis type VII Sly syndrome
• Mucopolysaccharidosis
• Mucormycosis
• Mucosulfatidosis
• Muenke syndrome

Mul

Muli–Mull

• Mulibrey nanism
• Müller–Barth–Menger syndrome
• Müllerian agenesis
• Müllerian aplasia
• Müllerian derivatives lymphangiectasia polydactyly
• Müllerian derivatives, persistent
• Müllerian duct abnormalities galactosemia
• Mulliez–Roux–Loterman syndrome

Mult

Multi

Multic–Multin

• Multicentric osteolysis nephropathy
• Multicentric reticulohistiocytosis
• Multifocal heterotopia
• Multifocal motor neuropathy
• Multifocal ventricular premature beats
• Multi-infarct dementia
• Multinodular goiter cystic kidney polydactyly

Multip

Multiple a – Multiple p

• Multiple acyl-CoA deficiency
• Multiple carboxylase deficiency, biotin responsive
• Multiple carboxylase deficiency, late onset
• Multiple carboxylase deficiency, propionic acidemia
• Multiple chemical sensitivity
• Multiple congenital anomalies mental retardation, growth failure and cleft lip palate
• Multiple congenital contractures
• Multiple contracture syndrome Finnish type
• Multiple endocrine neoplasia type 1
• Multiple endocrine neoplasia, type 2
• Multiple fibrofolliculoma familial
• Multiple hereditary exostoses
• Multiple joint dislocations metaphyseal dysplasia
• Multiple myeloma
• Multiple organ failure
• Multiple pterygium syndrome lethal type
• Multiple pterygium syndrome

Multiple s – Multiple v

• Multiple sclerosis ichthyosis factor VIII deficiency
• Multiple sclerosis
• Multiple subcutaneous angiolipomas
• Multiple sulfatase deficiency
• Multiple synostoses syndrome 1
• Multiple system atrophy
• Multiple vertebral anomalies unusual facies

Mum–Mut

• Mumps
• Münchausen syndrome
• Münchausen syndrome by proxy
• Muscle-eye-brain syndrome
• Muscular atrophy ataxia retinitis pigmentosa diabetes mellitus
• Muscular dystrophy congenital infantile cataract hypogonadism
• Muscular dystrophy congenital, merosin negative
• Muscular dystrophy, facioscapulohumeral
• Muscular dystrophy Hutterite type
• Muscular dystrophy limb girdle type 2A, Erb type
• Muscular dystrophy limb-girdle autosomal dominant
• Muscular dystrophy limb-girdle type 2B, Myoshi type
• Muscular dystrophy limb-girdle with beta-sarcoglycan deficiency
• Muscular dystrophy limb-girdle with delta-sarcoglyan deficiency
• Muscular dystrophy white matter spongiosis
• Muscular dystrophy, congenital, merosin-positive
• Muscular dystrophy, Duchenne and Becker type
• Muscular dystrophy
• Muscular fibrosis multifocal obstructed vessels
• Muscular phosphorylase kinase deficiency
• Mutations in estradiol receptor

My

Mya–Myc • Mye–Myi • Myo • Myx

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Mya–Myc

• Myalgia eosinophilia associated with tryptophan
• Myalgic encephalomyelitis
• Myasthenia gravis congenital
• Myasthenia gravis
• Myasthenia, familial
• Mycetoma
• Mycobacterium avium complex infection
• Mycoplasmal pneumonia
• Mycosis fungoides lymphoma
• Mycosis fungoides, familial
• Mycosis fungoides
• Mycositis fungoides

Mye–Myi

• Myelinopathy
• Myelitis
• Myelocerebellar disorder
• Myelodysplasia
• Myelodysplastic syndromes
• Myelofibrosis, idiopathic
• Myelofibrosis
• Myelofibrosis-osteosclerosis
• Myeloid splenomegaly
• Myeloperoxidase deficiency
• Myhre–Ruvalcaba–Graham syndrome
• Myhre–Ruvalcaba–Kelley syndrome
• Myhre–School syndrome
• Myhre syndrome
• Myiasis

Myo

Myoa–Myon

• Myoadenylate deaminase deficiency
• Myocarditis
• Myocardium disorder
• Myoclonic dystonia
• Myoclonic epilepsy
• Myoclonic epilepsy with ragged red fibres (MERRF syndrome)
• Myoclonic progressive familial epilepsy
• Myoclonus ataxia
• Myoclonus cerebellar ataxia deafness
• Myoclonus epilepsy partial seizure
• Myoclonus hereditary progressive distal muscular atrophy
• Myoclonus progressive epilepsy of Unverricht and Lundborg
• Myoclonus
• Myofibrillar lysis
• Myofibroblastic tumors
• Myoglobinuria dominant form
• Myoglobinuria recurrent
• Myoglobinuria
• Myoneurogastrointestinal encephalopathy syndrome

Myop

• Myopathy and diabetes mellitus
• Myopathy cataract hypogonadism
• Myopathy congenital multicore with external ophthalmoplegia
• Myopathy growth and mental retardation hypospadias
• Myopathy Hutterite type
• Myopathy mitochondrial cataract
• Myopathy Moebius Robin syndrome
• Myopathy ophthalmoplegia hypoacousia areflexia
• Myopathy tubular aggregates
• Myopathy with lactic acidosis and sideroblastic anemia
• Myopathy with lysis of myofibrils
• Myopathy, centronuclear
• Myopathy, desmin storage
• Myopathy, McArdle type
• Myopathy, myotubular
• Myopathy, X-linked, with excessive autophagy
• Myopathy
• Myophosphorylase deficiency
• Myopia
• Myopia, infantile severe
• Myopia, severe
• Myotubular myopathy

Myos–Myot

• Myositis ossificans post-traumatic
• Myositis ossificans progressiva
• Myositis ossificans
• Myositis, inclusion body
• Myositis
• Myotonia atrophica
• Myotonia mental retardation skeletal anomalies

Myx

• Myxedema
• Myxoid liposarcoma
• Myxoma-spotty pigmentation-endocrine overactivity
• Myxomatous peritonitis
• Myxozoa