Disease Index

9,486 diseases
Machado-Joseph disease type 1
Machado-Joseph disease type 1 is a rare, usually severe subtype of Machado-Joseph disease (SCA3/MJD, see this term) characterized by the presence of marked pyramidal and extrapyramidal signs
Machado-Joseph disease type 2
Machado-Joseph disease type 3
Machado-Joseph disease type 3 is a subtype of Machado-Joseph disease (SCA3/MJD, see this term) of milder severity characterized by late onset, slower progression, and peripheral amyotrophy
macrocephaly-autism syndrome
human disease
MeSH: C565342
Macrocephaly-capillary malformation
disease
MeSH: C536142
macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome
human disease
macrocephaly-short stature-paraplegia syndrome
MeSH: C537718
macrocephaly-spastic paraplegia-dysmorphism syndrome
MeSH: C563963
macrocephaly, dysmorphic facies, and psychomotor retardation
human disease
macrocystic lymphatic malformation
human disease
macrodactylia of fingers
Human disease
ICD: Q74.0MeSH: C537720
macrodactylia of toes
Human disease
MeSH: C537719
Macrodactyly of fingers, bilateral
human disease
Macrodactyly of fingers, unilateral
human disease
Macrodactyly of toes, bilateral
human disease
Macrodactyly of toes, unilateral
human disease
macroglossia
enlargement of the tongue
ICD: Q38.2MeSH: D008260
macrophage activation syndrome
complication of several chronic rheumatic diseases of childhood
MeSH: D055501
macrophage or histiocytic tumor
human disease
macrophagic myofasciitis
human disease
MeSH: C537829
Macrosomia-microphthalmia-cleft palate syndrome
human disease
ICD: Q87.0MeSH: C537830
macrostomia
unusually wide mouth
ICD: Q18.4MeSH: D008265
macrostomia-preauricular tags-external ophthalmoplegia syndrome
macrothrombocytopenia with mitral valve insufficiency
human disease
macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome
human disease
macular amyloidosis
macular coloboma-cleft palate-hallux valgus syndrome
MeSH: C565686
macular corneal dystrophy
corneal dystrophy that is characterized by corneal haze, severe photophobia at night ,gradual vision impairment ,bilateral loss of vision, eventually necessitating corneal transplantation resulting from progressive punctate opacities in the cornea
macular degeneration
retinal degeneration characterized by gradual deterioration of light-sensing cells in the tissues at the back of the eye
MeSH: D008268
macular dystrophy, vitelliform, 3
human disease
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