DOID:1455
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-
geographic tongue
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Aliases:
-
Glossitis areata exfoliativa
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Pityriasis linguae
-
benign migratory glossitis
|
|
|
Homo sapiens (human)
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|
DOID:6098
|
-
thalamic neoplasm
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Aliases:
-
malignant neoplasm of thalamus
-
malignant tumor of Thalamus
-
tumor of Thalamus
|
|
|
Homo sapiens (human)
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|
DOID:4648
|
-
familial retinoblastoma
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Aliases:
-
Hereditary Retinoblastoma
|
|
|
Homo sapiens (human)
|
|
DOID:14753
|
-
isovaleric acidemia
-
Aliases:
-
Isovaleryl-CoA dehydrogenase deficiency
-
isovaleric acid CoA dehydrogenase deficiency
-
isovaleric aciduria
|
|
|
Homo sapiens (human)
|
|
DOID:1171
|
-
hyperlipoproteinemia type V
-
Aliases:
-
Fredrickson type V lipaemia
-
familial hyperlipoproteinemia type V
-
familial type 5 hyperlipoproteinemia
|
|
|
Homo sapiens (human)
|
|
DOID:655
|
-
inherited metabolic disorder
-
Aliases:
-
Inborn Errors of Metabolism
-
Metabolic hereditary disorder
-
inborn metabolism disorder
|
|
|
Homo sapiens (human)
|
|
DOID:2660
|
|
|
|
Homo sapiens (human)
|
|
DOID:3168
|
-
squamous cell neoplasm
-
Aliases:
-
Epidermoid cell tumor
-
squamous cell tumor
|
|
|
Homo sapiens (human)
|
|
DOID:0080566
|
-
congenital disorder of glycosylation In
-
Aliases:
-
congenital disorder of glycosylation 1n
|
|
|
Homo sapiens (human)
|
|
DOID:2636
|
-
ovarian Brenner tumor
-
Aliases:
-
benign ovarian Brenner tumor
-
benign ovarian Brenner tumour
-
ovarian Brenner tumour
|
|
|
Homo sapiens (human)
|
|
DOID:13800
|
-
inclusion conjunctivitis
-
Aliases:
-
Chlamydial conjunctivitis
-
Inclusion blennorrhoea
-
adult inclusion conjunctivitis
-
inclusion blenorrhea
|
|
|
Homo sapiens (human)
|
|
DOID:0110587
|
-
autosomal dominant nonsyndromic deafness 66
-
Aliases:
-
DFNA66
-
autosomal dominant deafness 66
|
|
|
Homo sapiens (human)
|
|
DOID:0080596
|
-
hyper IgE recurrent infection syndrome 4
|
|
|
Homo sapiens (human)
|
|
DOID:0090105
|
-
autosomal recessive hypercholesterolemia
-
Aliases:
-
ARH
-
ARH1
-
ARH2
-
FHCB1
-
FHCB2
-
autosomal recessive hypercholesterolemia 1
-
autosomal recessive hypercholesterolemia 2
-
familial autosomal recessive hypercholesterolemia
|
|
|
Homo sapiens (human)
|
|
DOID:0090109
|
-
autosomal dominant hypocalcemia
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:890
|
-
mitochondrial encephalomyopathy
|
|
|
Homo sapiens (human)
|
|
DOID:8618
|
-
oral cavity cancer
-
Aliases:
-
malignant neoplasm of floor of mouth
|
|
|
Homo sapiens (human)
|
|
DOID:0060216
|
-
Cogan syndrome
-
Aliases:
-
Cogan's syndrome
-
diffuse interstitual keratitis
|
|
|
Homo sapiens (human)
|
|
DOID:0090122
|
-
aromatase excess syndrome
-
Aliases:
-
AEXS
-
familial hyperestrogenism
-
hereditary prepubertal gynecomastia
-
increased aromatase activity
|
|
|
Homo sapiens (human)
|
|
DOID:1703
|
-
Richter's syndrome
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:0090091
|
-
hypogonadotropic hypogonadism 23 with or without anosmia
-
Aliases:
-
46,XY DSD due to LHB deficiency
-
46,XY DSD due to luteinizing hormone subunit beta deficiency
-
46,XY disorder of sex development due to LHB deficiency
-
46,XY disorder of sex development due to luteinizing hormone subunit beta deficiency
-
Leydig cell hypoplasia due to luteinizing hormone subunit beta deficiency
-
Pasqualini syndrome
-
fertile eunuch syndrome
-
leydig cell hypoplasia due to LHB deficiency
|
|
|
Homo sapiens (human)
|
|
DOID:0060398
|
-
chromosome 16p11.2 deletion syndrome, 220-kb
-
Aliases:
-
distal 16p11.2 microdeletion syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:7210
|
|
|
|
Homo sapiens (human)
|
|
DOID:10825
|
-
essential hypertension
-
Aliases:
-
idiopathic hypertension
-
primary hypertension
|
|
|
Homo sapiens (human)
|
|
DOID:0110035
|
-
Alzheimer's disease 2
-
Aliases:
-
AD2
-
Alzheimer disease 2, late onset
-
Alzheimer disease associated with APOE4
-
Alzheimer disease-2
|
|
|
Homo sapiens (human)
|
|