List of diseases (M)

This is a list of diseases starting with the letter "M".

Ma

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

Mal

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

Man

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

Mc

Me

Mea–Med
  • Meacham–Winn–Culler syndrome
  • Meadows syndrome, names for:
  • 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

Men

Mend–Meno

Ment
Menta
Mental

Mental d – Mental m

  • Mental deficiency-epilepsy-endocrine disorders
  • Mental mixed retardation deafness 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-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

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

Mi

Mib
  • Mibies syndrome

Mic

Mich–Mick

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 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

Ml–Mn
  • MLS syndrome
  • MMEP syndrome
  • MMT syndrome
  • MN1
  • MNGIE syndrome

Mo

Mob–Mom

Mon–Moo

Mor–Moy
  • Morel's ear
  • Moreno–Zachai–Kaufman syndrome
  • Morgani–Turner–Albright 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 (Müllerian 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
  • 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
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

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

Mye–Myi

Myo

Myoa–Myon

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
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