DOID:1142
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Homo sapiens (human)
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DOID:0110229
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-
cataract 6 multiple types
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Aliases:
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|
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Homo sapiens (human)
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DOID:9268
|
-
glycine encephalopathy
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Aliases:
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Non-ketotic hyperglycinemia
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nonketotic hyperglycinemia
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|
|
Homo sapiens (human)
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DOID:0110205
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-
Charcot-Marie-Tooth disease dominant intermediate E
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Aliases:
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CMTDIE
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Charcot-Marie-Tooth disease-nephropathy syndrome
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Charcot-Marie-Tooth neuropathy with focal segmental glomerulonephritis
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autosomal dominant intermediate Charcot-Marie-Tooth disease type E
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|
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Homo sapiens (human)
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DOID:0060395
|
-
chromosome 15q24 deletion syndrome
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Aliases:
-
15q24 microdeletion syndrome
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|
|
Homo sapiens (human)
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DOID:1793
|
-
pancreatic cancer
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Aliases:
-
Ca body of pancreas
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Ca head of pancreas
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Ca tail of pancreas
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malignant neoplasm of body of pancreas
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malignant neoplasm of head of pancreas
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malignant neoplasm of tail of pancreas
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pancreas neoplasm
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pancreatic neoplasm
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pancreatic tumor
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|
|
Homo sapiens (human)
|
DOID:9719
|
-
neovascular inflammatory vitreoretinopathy
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Aliases:
-
ADNIV
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Retinitis proliferans
-
autosomal dominant neovascular inflammatory vitreoretinopathy
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proliferative vitreoretinopathy
|
|
|
Homo sapiens (human)
|
DOID:2012
|
-
Nezelof syndrome
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Aliases:
-
Nezelof's syndrome
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T-cell immunodeficiency with thymic aplasia
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TIDTA
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thymic aplasia
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thymic dysplasia with normal immunoglobulins
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|
|
Homo sapiens (human)
|
DOID:13374
|
-
fibrodysplasia ossificans progressiva
-
Aliases:
-
Stone Man Syndrome
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myositis ossificans progressiva
-
progressive myositis ossificans
-
progressive ossifying myositis
|
|
|
Homo sapiens (human)
|
DOID:5566
|
|
|
|
Homo sapiens (human)
|
DOID:2755
|
-
Mycobacterium avium complex disease
-
Aliases:
-
Infection due to Mycobacterium intracellulare
-
MAC disease
-
Mycobacterium Avium Infection
-
Mycobacterium avium Complex
|
|
|
Homo sapiens (human)
|
DOID:10241
|
-
thalassemia
-
Aliases:
-
Sickle-cell thalassemia with crisis
-
Sickle-cell thalassemia without crisis
-
thalassemia Hb-S disease with crisis
-
thalassemia Hb-S disease without crisis
|
|
|
Homo sapiens (human)
|
DOID:0050486
|
|
|
|
Homo sapiens (human)
|
DOID:0040085
|
|
|
|
Homo sapiens (human)
|
DOID:9253
|
-
gastrointestinal stromal tumor
-
Aliases:
-
GANT
-
GIST
-
Stromal tumor of gastrointestinal tract
-
Stromal tumour of gastrointestinal tract
-
gastrointestinal stromal tumour
|
|
|
Homo sapiens (human)
|
DOID:10690
|
-
mastitis
-
Aliases:
-
Inflammatory breast disease
-
Inflammatory disease of breast
-
breast inflammation
|
|
|
Homo sapiens (human)
|
DOID:10175
|
-
optic papillitis
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:468
|
-
intramuscular hemangioma
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:10325
|
-
silicosis
-
Aliases:
-
Pneumoconiosis due to silicates
-
Silica pneumoconiosis
-
Silicotic fibrosis of lung
-
silicotuberculosis
|
|
|
Homo sapiens (human)
|
DOID:0060415
|
-
chromosome 2p16.1-p15 deletion syndrome
-
Aliases:
-
2p15p16.1 microdeletion syndrome
|
|
|
Homo sapiens (human)
|
DOID:0050885
|
-
IMAGe syndrome
-
Aliases:
-
intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, genital abnormalities
|
|
|
Homo sapiens (human)
|
DOID:0110509
|
-
autosomal recessive nonsyndromic deafness 53
-
Aliases:
-
DFNB53
-
autosomal recessive deafness 53
|
|
|
Homo sapiens (human)
|
DOID:0050567
|
|
|
|
Homo sapiens (human)
|
DOID:0110159
|
-
Charcot-Marie-Tooth disease type 2B
-
Aliases:
-
CMT2B
-
Charcot-Marie-Tooth neuropathy type 2B
-
HMSN IIB
-
HMSN2B
-
autosomal dominant Charcot-Marie-Tooth disease type 2B
-
hereditary motor and sensory nueropathy IIB
|
|
|
Homo sapiens (human)
|
DOID:13272
|
-
Klebsiella pneumonia
-
Aliases:
-
Pneumonia due to Klebsiella pneumoniae
-
Pneumonia due to Klebsiella pneumoniae (disorder)
|
|
|
Homo sapiens (human)
|