DOID:0110787
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hereditary spastic paraplegia 36
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Aliases:
-
SPG36
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autosomal dominant spastic paraplegia 36
-
autosomal dominant spastic paraplegia type 36
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|
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Homo sapiens (human)
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DOID:1094
|
-
attention deficit hyperactivity disorder
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Aliases:
-
ADHD
-
attention deficit disorder
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hyperkinetic disorder
|
|
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Homo sapiens (human)
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DOID:0110254
|
-
cataract 25
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Aliases:
-
CCSSO
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CTRCT25
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central pouch-like cataract with sutural opacities
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central saccular cataract with sutural opacities
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early-onset cataract with Y-shaped suture opacities
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|
|
Homo sapiens (human)
|
DOID:0060580
|
-
Noonan syndrome 2
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Aliases:
|
|
|
Homo sapiens (human)
|
DOID:10328
|
|
|
|
Homo sapiens (human)
|
DOID:0110448
|
-
dilated cardiomyopathy 1HH
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Aliases:
|
|
|
Homo sapiens (human)
|
DOID:9245
|
-
Alagille syndrome
-
Aliases:
-
Alagille-Watson syndrome
-
Arteriohepatic dysplasia
|
|
|
Homo sapiens (human)
|
DOID:11486
|
-
Horner's syndrome
-
Aliases:
-
Bernard Horner syndrome
-
Horner syndrome
-
cervical sympathetic paralysis
|
|
|
Homo sapiens (human)
|
DOID:1686
|
|
|
|
Homo sapiens (human)
|
DOID:678
|
-
progressive supranuclear palsy
-
Aliases:
-
Steele-Richardson-Olszewski syndrome
-
progressive supranuclear ophthalmoplegia
|
|
|
Homo sapiens (human)
|
DOID:0050801
|
-
androgenic alopecia
-
Aliases:
-
alopecia androgenetica, male pattern baldness
-
androgenetic alopecia
|
|
|
Homo sapiens (human)
|
DOID:0110444
|
-
dilated cardiomyopathy 1X
-
Aliases:
-
CMD1X
-
dilated cardiomyopathy with mild or no proximal muscle weakness
|
|
|
Homo sapiens (human)
|
DOID:0070124
|
-
congenital nongoitrous hypothyroidism 2
-
Aliases:
-
CHNG2
-
congenital hypothyroidism due to thyroid dysgenesis or hypoplasia
|
|
|
Homo sapiens (human)
|
DOID:0080070
|
-
mucolipidosis II alpha/beta
-
Aliases:
-
I-cell disease
-
inclusion-cell disease
-
mucolipidosis II
|
|
|
Homo sapiens (human)
|
DOID:12842
|
-
Guillain-Barre syndrome
-
Aliases:
-
Infectious neuronitis
-
Post-infectious polyneuritis
-
Postinfectious polyneuritis
-
acute infective polyneuritis
-
acute inflammatory demyelinating polyradiculopathy
-
acute postinfectious polyneuropathy
|
|
|
Homo sapiens (human)
|
DOID:0080502
|
-
GM1 gangliosidosis type 1
|
|
|
Homo sapiens (human)
|
DOID:0060745
|
-
Doyne honeycomb retinal dystrophy
-
Aliases:
-
DHRD
-
Doyne honeycomb degeneration of retina
|
|
|
Homo sapiens (human)
|
DOID:0110592
|
-
autosomal dominant nonsyndromic deafness 70
-
Aliases:
-
DFNA70
-
autosomal dominant deafness 70
|
|
|
Homo sapiens (human)
|
DOID:9649
|
|
|
|
Homo sapiens (human)
|
DOID:0060844
|
-
Norrie disease
-
Aliases:
-
Episkopi blindness
-
Norrie-Warburg disease
-
atrophia bulborum hereditaria
|
|
|
Homo sapiens (human)
|
DOID:10871
|
-
age related macular degeneration
-
Aliases:
-
Age Related Maculopathies
-
Age Related Maculopathy
-
Senile macular degeneration
-
Senile macular retinal degeneration
-
age-related macular degeneration
|
|
|
Homo sapiens (human)
|
DOID:3284
|
-
thymic carcinoma
-
Aliases:
-
Thymoma, malignant
-
malignant Thymoma
|
|
|
Homo sapiens (human)
|
DOID:5213
|
-
chronic inflammatory demyelinating polyradiculoneuropathy
|
|
|
Homo sapiens (human)
|
DOID:1073
|
|
|
|
Homo sapiens (human)
|
DOID:11723
|
-
Duchenne muscular dystrophy
-
Aliases:
-
Muscular dystrophy, Duchenne
|
|
|
Homo sapiens (human)
|