List of diseases

A list of diseases in the English wikipedia.

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

Contents 1 Ma 1.1 Mac 1.1.1 Maci-Macr 1.1.2 Macu 1.2 Mad-Mag 1.3 Mal 1.3.1 Mala-Mall 1.3.2 Malo-Malp 1.4 Man 1.5 Mar 1.5.1 Mara-Marg 1.5.2 Mari-Mart 1.6 Mas-May 2 Mc 3 Me 3.1 Mea-Med 3.2 Meg-Mei 3.3 Mel-Mem 3.4 Men 3.4.1 Mend-Meno 3.4.2 Ment 3.4.2.1 Menta 3.4.2.1.1 Mental 3.5 Mer-Mes 3.6 Met 3.6.1 Meta 3.6.2 Meth 3.7 Mev-Mey 4 Mi 4.1 Mic 4.1.1 Mich-Mick 4.1.2 Micr 4.1.2.1 Mircre 4.1.2.2 Micro 4.1.2.2.1 Microb 4.1.2.2.2 Microc 4.1.2.2.3 Microd-Microv 4.1.3 Micu 4.2 Mid-Mir 4.3 Mis-Mix 5 Ml-Mn 6 Mo 6.1 Mob-Mom 6.2 Mon-Moo 6.3 Mor-Moy 7 Mp-Mt 8 Mu 8.1 Muc-Mue 8.2 Mul 8.2.1 Muli-Mull 8.2.2 Mult 8.2.2.1 Multi 8.2.2.1.1 Multic-Multin 8.2.2.1.2 Multip 8.3 Mum-Mut 9 My 9.1 Mya-Myc 9.2 Mye-Myi 9.3 Myo 9.3.1 Myoa-Myon 9.3.2 Myop 9.3.3 Myos-Myot 9.4 Myx

Ma

Mac

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

Mad-Mag

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

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 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 hyperthermia
• Malignant mesenchymal tumor
• Malignant mixed Mullerian 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 type II
• Marfan Syndrome type III
• Marfan Syndrome type IV
• Marfan Syndrome type V
• Marfan syndrome
• 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 Sjogren like syndrome
• Marinesco-Sjogren 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 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

• 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
• 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 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
• Mental retardation-polydactyly-uncombable hair

Mer-Mes

• Mercury poisoning
• 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 adenosyl transferase 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

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 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 quadriplegia
• Microcephaly, holoprosencephaly, and intrauterine growth retardation
• Microcephaly, primary autosomal recessive
• Microcephaly

Microco

• Microcoria, congenital
• Microcornea corectopia 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 camptodactyly mental retardation
• Microphthalmia cataract
• Microphthalmia diaphragmatic hernia Fallot
• Microphthalmia mental deficiency
• Microphthalmia microtia fetal akinesia
• Microphthalmia, Lentz type
• Microphthalmia
• 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' Disease
• Mikulicz syndrome
• Miller Fisher syndrome
• Miller-Dieker syndrome
• Milner Khallouf Gibson syndrome
• MILS syndrome
• Minkowski-Chauffard disease
• Minoxidil antenatal infection
• Miosis, congenital
• 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 Diseases
• 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 sclerosing bone dystrophy

Ml-Mn

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

Mo

Mob-Mom

• Mobius syndrome
• MODY syndrome
• Moebius axonal neuropathy hypogonadism
• Moebius syndrome
• Moerman Van den berghe Fryns syndrome
• Moeschler Clarren syndrome
• Mohr syndrome
• Mohr-Tranebjaerg 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
• Morhosseini Holmes Walton syndrome
• 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 (Mullerian Agenesis)
• MSBD syndrome
• MTHFR deficiency

Mu

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
• Mucosulfatidosis
• Muenke Syndrome

Mul

Muli-Mull

• Mulibrey Nanism syndrome
• Muller Barth Menger syndrome
• Mullerian agenesis
• Mullerian aplasia
• Mullerian derivatives lymphangiectasia polydactyly
• Mullerian derivatives, persistent
• Mullerian duct abnormalities galactosemia
• Mulliez Roux Loterman syndrome

Mult

Multi

Multic-Multin

• Multicentric osteolysis nephropathy
• Multicentric reticulohistiocytosis
• Multifocal heterotopia
• Multifocal motor neuropathy with conduction block
• Multifocal ventricular premature beats
• 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
• Munchausen by proxy syndrome
• 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

• 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 progressive familial epilepsy
• Myoclonus ataxia
• Myoclonus cerebellar ataxia deafness
• Myoclonus epilepsy partial seizure
• Myoclonus epilepsy
• Myoclonus hereditary progressive distal muscular atrophy
• Myoclonus progressive epilepsy of Unverricht and Lundborg
• Myoclonus with epilepsy with ragged red fibers (mitochondria)
• 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