DOID:13208
|
-
background diabetic retinopathy
-
Aliases:
-
Non proliferative diabetic retinopathy
-
Non-Proliferative Diabetic Retinopathy
|
|
|
Homo sapiens (human)
|
DOID:1492
|
-
obsolete eye and adnexa disease
|
|
|
Homo sapiens (human)
|
DOID:11994
|
|
|
|
Homo sapiens (human)
|
DOID:2272
|
-
vulvovaginal candidiasis
-
Aliases:
-
Candidal cervix
-
Candidal vulvovaginitis
-
Candidiasis of vulva and vagina
-
Monilial vulvovaginitis
|
|
|
Homo sapiens (human)
|
DOID:13724
|
|
|
|
Homo sapiens (human)
|
DOID:5509
|
|
|
|
Homo sapiens (human)
|
DOID:6271
|
-
gastric cardia adenocarcinoma
-
Aliases:
-
adenocarcinoma of Cardia of stomach
|
|
|
Homo sapiens (human)
|
DOID:10908
|
-
hydrocephalus
-
Aliases:
-
hydrocephalus, X-linked
-
hydrocephalus, nonsyndromic, autosomal recessive
|
|
|
Homo sapiens (human)
|
DOID:0050560
|
-
Walker-Warburg syndrome
-
Aliases:
-
HARD syndrome
-
cerebroocular dysplasia-muscular dystrophy syndrome
|
|
|
Homo sapiens (human)
|
DOID:0111237
|
-
congenital muscular dystrophy-dystroglycanopathy type A1
-
Aliases:
-
MDDGA1
-
Walker-Warburg syndrome or muscle-eye-brain disease, POMT1-related
-
congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A1
|
|
|
Homo sapiens (human)
|
DOID:1686
|
|
|
|
Homo sapiens (human)
|
DOID:83
|
|
|
|
Homo sapiens (human)
|
DOID:0060287
|
|
|
|
Homo sapiens (human)
|
DOID:0060673
|
|
|
|
Homo sapiens (human)
|
DOID:1573
|
-
communicating hydrocephalus
|
|
|
Homo sapiens (human)
|
DOID:14159
|
-
obstructive hydrocephalus
|
|
|
Homo sapiens (human)
|
DOID:14524
|
-
senile degeneration of brain
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:2785
|
-
Dandy-Walker syndrome
-
Aliases:
-
Atresia of foramina of Magendie and Luschka
|
|
|
Homo sapiens (human)
|
DOID:8501
|
-
fundus dystrophy
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:5327
|
|
|
|
Homo sapiens (human)
|
DOID:11723
|
-
Duchenne muscular dystrophy
-
Aliases:
-
Muscular dystrophy, Duchenne
|
|
|
Homo sapiens (human)
|
DOID:0050557
|
-
congenital muscular dystrophy
|
|
|
Homo sapiens (human)
|
DOID:0060255
|
-
rippling muscle disease 2
-
Aliases:
-
autosomal dominant limb-girdle muscular dystrophy type 1C
|
|
|
Homo sapiens (human)
|
DOID:0080092
|
-
myofibrillar myopathy 1
-
Aliases:
-
autosomal recessive limb-girdle muscular dystrophy type 2R
-
desminopathy
|
|
|
Homo sapiens (human)
|
DOID:0070247
|
-
autosomal dominant Emery-Dreifuss muscular dystrophy 2
-
Aliases:
-
EDMD2
-
EMD2
-
Emery-Dreifuss muscular dystrophy 2, autosomal dominant
-
Emery-Dreifuss muscular dystrophy, autosomal dominant
-
Hauptmann-Thannhauser muscular dystrophy
-
autosomal dominant limb-girdle muscular dystrophy type 1B
-
muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant
-
scapuloilioperoneal atrophy with cardiopathy
|
|
|
Homo sapiens (human)
|