DOID:0110859
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polycystic kidney disease 2
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Aliases:
-
Apkd2
-
Pkd2
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Polycystic Kidney Disease, Adult, Type II
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Homo sapiens (human)
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DOID:0070186
|
-
Y-linked spermatogenic failure 1
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Aliases:
-
SPGFY1
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Y-linked Sertoli cell-only syndrome
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type I Sertoli cell-only syndrome
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Homo sapiens (human)
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|
DOID:170
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-
endocrine gland cancer
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Aliases:
-
Endocrine tumor
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endocrine neoplasm
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malignant Endocrine tumor
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malignant neoplasm of endocrine gland
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malignant tumour of endocrine gland
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neoplasm of endocrine gland
-
neoplasm of endocrine system
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Homo sapiens (human)
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DOID:1325
|
-
bronchus cancer
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Aliases:
-
malignant neoplasm of bronchus and lung
-
malignant neoplasm of bronchus or lung
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|
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Homo sapiens (human)
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|
DOID:12506
|
-
Bell's palsy
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Aliases:
-
Bell palsy
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Bell's (facial) palsy
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|
|
Homo sapiens (human)
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|
DOID:0070519
|
-
early-onset vitamin B6-dependent epilepsy 4
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Aliases:
-
AASA dehydrogenase deficiency
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EPEO4
-
PDE-ALDH7A1
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antiquitin deficiency
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|
|
Homo sapiens (human)
|
|
DOID:0080561
|
-
congenital disorder of glycosylation Ii
-
Aliases:
-
congenital disorder of glycosylation 1i
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|
|
Homo sapiens (human)
|
|
DOID:0060738
|
-
junctional epidermolysis bullosa non-Herlitz type
-
Aliases:
-
GABEB
-
JEB-nH gen
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JEN-nH
-
generalized atrophic benign epidermolysis bullosa
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generalized junctional epidermolysis bullosa, non-Herlitz type
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junctional epidermolysis bullosa generalisata mitis
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junctional epidermolysis bullosa, Disentis type
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|
|
Homo sapiens (human)
|
|
DOID:14735
|
-
hereditary angioedema
-
Aliases:
-
HANE
-
Hereditary angioneurotic edema
|
|
|
Homo sapiens (human)
|
|
DOID:2273
|
|
|
|
Homo sapiens (human)
|
|
DOID:999
|
-
hypereosinophilic syndrome
-
Aliases:
-
Eosinophilic leukocytosis
-
eosinophilia
|
|
|
Homo sapiens (human)
|
|
DOID:14757
|
-
Ehlers-Danlos syndrome hypermobility type
-
Aliases:
-
Ehlers-Danlos syndrome, type 3
-
type III Ehlers-Danlos syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:0110135
|
-
Bardet-Biedl syndrome 13
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:13372
|
-
alpha 1-antitrypsin deficiency
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:0110808
|
-
hereditary spastic paraplegia 56
-
Aliases:
-
SPG56
-
autosomal recessive spastic paraplegia 56
-
autosomal recessive spastic paraplegia type 56
|
|
|
Homo sapiens (human)
|
|
DOID:0050452
|
-
mevalonic aciduria
-
Aliases:
-
Mevalonate Kinase Deficiency
|
|
|
Homo sapiens (human)
|
|
DOID:14203
|
-
childhood type dermatomyositis
-
Aliases:
-
Juvenile dermatomyositis
-
childhood Dermatomyositis
|
|
|
Homo sapiens (human)
|
|
DOID:9766
|
-
xanthogranulomatous cholecystitis
|
|
|
Homo sapiens (human)
|
|
DOID:0110568
|
-
autosomal dominant nonsyndromic deafness 43
-
Aliases:
-
DFNA43
-
autosomal dominant deafness 43
|
|
|
Homo sapiens (human)
|
|
DOID:3137
|
-
obsolete multiple symmetrical lipomatosis
|
|
|
Homo sapiens (human)
|
|
DOID:5695
|
-
childhood liposarcoma
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:10534
|
-
stomach cancer
-
Aliases:
-
gastric cancer
-
gastric neoplasm
|
|
|
Homo sapiens (human)
|
|
DOID:495
|
-
sclerosing hemangioma
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:8337
|
-
appendicitis
-
Aliases:
-
acute appendicitis
-
acute appendicitis with generalized peritonitis
-
acute appendicitis with peritoneal abscess
|
|
|
Homo sapiens (human)
|
|
DOID:5773
|
-
oral submucous fibrosis
-
Aliases:
-
Oral cavity Submucous Fibrosis
-
Oral submucosal fibrosis
-
Oral submucosal fibrosis, including of tongue
|
|
|
Homo sapiens (human)
|
|