DOID:1455
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-
geographic tongue
-
Aliases:
-
Glossitis areata exfoliativa
-
Pityriasis linguae
-
benign migratory glossitis
|
|
|
Homo sapiens (human)
|
|
DOID:2848
|
|
|
|
Homo sapiens (human)
|
|
DOID:0070230
|
-
benign recurrent intrahepatic cholestasis
-
Aliases:
-
BRIC
-
Summerskill-Walshe-Tygstrup syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:0110550
|
-
autosomal dominant nonsyndromic deafness 20
-
Aliases:
-
DFNA20
-
DFNA26
-
autosomal dominant deafness 20
|
|
|
Homo sapiens (human)
|
|
DOID:0050834
|
|
|
|
Homo sapiens (human)
|
|
DOID:10844
|
-
Japanese encephalitis
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:10968
|
-
spastic monoplegia
-
Aliases:
-
Monoplegic infantile cerebral palsy
-
infantile monoplegic cerebral palsy
-
spastic monoplegic cerebral palsy
|
|
|
Homo sapiens (human)
|
|
DOID:0111380
|
-
solitary median maxillary central incisor
-
Aliases:
-
SMMCI
-
fused incisors
-
single central maxillary incisor
-
single median maxillary central incisor
-
single upper central incisor
|
|
|
Homo sapiens (human)
|
|
DOID:6098
|
-
thalamic neoplasm
-
Aliases:
-
malignant neoplasm of thalamus
-
malignant tumor of Thalamus
-
tumor of Thalamus
|
|
|
Homo sapiens (human)
|
|
DOID:4648
|
-
familial retinoblastoma
-
Aliases:
-
Hereditary Retinoblastoma
|
|
|
Homo sapiens (human)
|
|
DOID:9743
|
|
|
|
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:5504
|
|
|
|
Homo sapiens (human)
|
|
DOID:0081120
|
-
Graves ophthalmopathy
-
Aliases:
-
Graves orbitopathy
-
Thyroid associated ophthalmopathy
-
thyroid eye disease
|
|
|
Homo sapiens (human)
|
|
DOID:0110187
|
-
Charcot-Marie-Tooth disease type 4K
-
Aliases:
-
CMT4K
-
SURF1-related CMT4
-
SURF1-related Charcot-Marie-Tooth disease type 4
-
SURF1-related severe demyelinating Charcot-Marie-Tooth disease
-
autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4K
-
autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy type 4K
|
|
|
Homo sapiens (human)
|
|
DOID:655
|
-
inherited metabolic disorder
-
Aliases:
-
Inborn Errors of Metabolism
-
Metabolic hereditary disorder
-
inborn metabolism disorder
|
|
|
Homo sapiens (human)
|
|
DOID:0080190
|
-
malignant epithelioid hemangioendothelioma
|
|
|
Homo sapiens (human)
|
|
DOID:2660
|
|
|
|
Homo sapiens (human)
|
|
DOID:0060400
|
-
chromosome 16p12.2-p11.2 deletion syndrome
-
Aliases:
-
16p11.2-p12.2 microdeletion syndrome
-
16p11.2p12.2 microdeletion syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:3168
|
-
squamous cell neoplasm
-
Aliases:
-
Epidermoid cell tumor
-
squamous cell tumor
|
|
|
Homo sapiens (human)
|
|
DOID:5679
|
|
|
|
Homo sapiens (human)
|
|
DOID:2636
|
-
ovarian Brenner tumor
-
Aliases:
-
benign ovarian Brenner tumor
-
benign ovarian Brenner tumour
-
ovarian Brenner tumour
|
|
|
Homo sapiens (human)
|
|
DOID:1475
|
-
lymphangioma
-
Aliases:
-
Congenital lymphangioma
-
benign lymphangioma
|
|
|
Homo sapiens (human)
|
|
DOID:0050795
|
|
|
|
Homo sapiens (human)
|
|
DOID:0001816
|
|
|
|
Homo sapiens (human)
|
|