DOID:0060462
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Desbuquois dysplasia
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Aliases:
-
Desbuquois syndrome
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micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification
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|
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Homo sapiens (human)
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DOID:1595
|
-
melancholic depression
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Aliases:
-
endogenous depression
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major depressive disorder with melancholic features
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melancholia
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|
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Homo sapiens (human)
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DOID:0110859
|
-
polycystic kidney disease 2
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Aliases:
-
Apkd2
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Pkd2
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Polycystic Kidney Disease, Adult, Type II
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|
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Homo sapiens (human)
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DOID:0110679
|
-
congenital myasthenic syndrome 4C
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Aliases:
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CMS Id
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CMS1D
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CMS4C
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FIM1
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congenital myasthenic syndrome 4C associated with acetylcholine receptor deficiency
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congenital myasthenic syndrome type Id
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familial infantile myasthenia 1
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|
|
Homo sapiens (human)
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DOID:750
|
-
peptic ulcer disease
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Aliases:
-
acute peptic ulcer with hemorrhage
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acute peptic ulcer with hemorrhage and perforation
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acute peptic ulcer without hemorrhage and without perforation
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|
|
Homo sapiens (human)
|
DOID:1742
|
-
drug psychosis
-
Aliases:
-
Drug-induced psychosis
-
Drug-induced psychotic disorder
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|
|
Homo sapiens (human)
|
DOID:0111385
|
-
inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1
-
Aliases:
-
IBMPFD1
-
MSP1
-
multisystem proteinopathy 1
|
|
|
Homo sapiens (human)
|
DOID:417
|
-
autoimmune disease
-
Aliases:
-
autoimmune hypersensitivity disease
-
hypersensitivity reaction type II disease
|
|
|
Homo sapiens (human)
|
DOID:4926
|
-
bronchiolo-alveolar adenocarcinoma
-
Aliases:
-
Bronchioalveolar lung carcinoma
-
Bronchioloalveolar carcinoma
-
Minimally Invasive Lung Adenocarcinoma
|
|
|
Homo sapiens (human)
|
DOID:13250
|
|
|
|
Homo sapiens (human)
|
DOID:11254
|
-
Brill-Zinsser disease
-
Aliases:
-
Brill Zinsser disease
-
Brill's disease
-
Recrudescent typhus
|
|
|
Homo sapiens (human)
|
DOID:0110812
|
-
hereditary spastic paraplegia 61
-
Aliases:
-
SPG61
-
autosomal recessive spastic paraplegia 61
-
autosomal recessive spastic paraplegia type 61
|
|
|
Homo sapiens (human)
|
DOID:3210
|
-
Pelizaeus-Merzbacher disease
-
Aliases:
-
HLD1
-
Leukodystrophy, sudanophilic
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PMD
-
Pelizaeus Merzbacher brain sclerosis
-
Pelizaeus-Merzbacher brain sclerosis
-
diffuse familial brain sclerosis
-
hypomyelinating leukodystrophy 1
-
sudanophilic leukodystrophy, Paelizeus-Merzbacher type
|
|
|
Homo sapiens (human)
|
DOID:12382
|
-
complex partial epilepsy
-
Aliases:
-
Complex partial epileptic seizure
-
epilepsy, psychomotor
-
psychomotor epilepsy
|
|
|
Homo sapiens (human)
|
DOID:0110543
|
-
autosomal dominant nonsyndromic deafness 11
-
Aliases:
-
DFNA11
-
autosomal dominant deafness 11
|
|
|
Homo sapiens (human)
|
DOID:12384
|
|
|
|
Homo sapiens (human)
|
DOID:3410
|
-
carotid artery thrombosis
|
|
|
Homo sapiens (human)
|
DOID:0110551
|
-
autosomal dominant nonsyndromic deafness 21
-
Aliases:
-
DFNA21
-
autosomal dominant deafness 21
|
|
|
Homo sapiens (human)
|
DOID:0090026
|
-
split hand-foot malformation 6
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0050647
|
-
Arts syndrome
-
Aliases:
-
ARTS
-
Lethal ataxia with deafness and optic atrophy
-
MRXS18
-
MRXSARTS
-
fatal X-linked ataxia with deafness and loss of vision
-
syndromic X-linked mental retardation 18
-
syndromic X-linked mental retardation Arts type
|
|
|
Homo sapiens (human)
|
DOID:10590
|
|
|
|
Homo sapiens (human)
|
DOID:1474
|
-
aggressive periodontitis
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:3055
|
-
paratyphoid fever
-
Aliases:
-
Paratyphoid
-
Paratyphoid A fever
-
Paratyphoid B fever
-
Paratyphoid C fever
-
Paratyphoid fever A
-
Paratyphoid fever B
-
Paratyphoid fever C
-
paratyphoid a
-
paratyphoid b
-
paratyphoid c
|
|
|
Homo sapiens (human)
|
DOID:0111135
|
-
congenital generalized lipodystrophy type 1
-
Aliases:
-
Berardinelli-Seip Congenital Lipodystrophy, Type 1
-
Brunzell syndrome AGPAT2-related
|
|
|
Homo sapiens (human)
|
DOID:0050729
|
-
Chanarin-Dorfman syndrome
-
Aliases:
-
neutral lipid storage disease
|
|
|
Homo sapiens (human)
|