DOID:809
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|
|
|
Homo sapiens (human)
|
|
DOID:5299
|
-
endometrial clear cell adenocarcinoma
-
Aliases:
-
Clear cell carcinoma of Endometrium
|
|
|
Homo sapiens (human)
|
|
DOID:0060869
|
-
late-onset retinal degeneration
-
Aliases:
-
LORD
-
autosomal dominant late-onset retinal degeneration
|
|
|
Homo sapiens (human)
|
|
DOID:0060696
|
|
|
|
Homo sapiens (human)
|
|
DOID:6676
|
-
Froelich syndrome
-
Aliases:
-
Babinski-Froelich syndrome
-
Froehlich syndrome
-
Froehlich's syndrome
-
Froelich's syndrome
-
adiposogenital syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:2891
|
|
|
|
Homo sapiens (human)
|
|
DOID:4780
|
-
anti-basement membrane glomerulonephritis
-
Aliases:
-
anti-GBM glomerulonephritis
|
|
|
Homo sapiens (human)
|
|
DOID:0111394
|
-
mucopolysaccharidosis type IIIB
-
Aliases:
-
MPS3B
-
MPSIIIB
-
Mucopoly-saccharidosis type 3B
-
Mucopolysaccharidosis type 3B
-
N-acetyl-alpha-glucosaminidase deficiency
-
NAGLU deficiency
-
Sanfilippo syndrome type B
-
mucopolysaccharidosis type IIIB (Sanfilippo B)
|
|
|
Homo sapiens (human)
|
|
DOID:0070263
|
-
congenital disorder of glycosylation type IIk
-
Aliases:
-
CDG IIk
-
CDG syndrome type IIk
-
CDG2K
-
CDGIIdk
-
Carbohydrate deficient glycoprotein syndrome type IIk
-
Congenital disorder of glycosylation type 2k
-
TMEM165-CDG
|
|
|
Homo sapiens (human)
|
|
DOID:0110414
|
-
retinitis pigmentosa 3
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:14499
|
-
Fabry disease
-
Aliases:
-
Alpha-galactosidase A deficiency
-
Angiokeratoma Corporis Diffusum
-
Fabry Disease, Cardiac Variant
-
Fabry's disease
-
alpha galactosidase deficiency
-
deficiency of melibiase
|
|
|
Homo sapiens (human)
|
|
DOID:0110538
|
-
autosomal recessive nonsyndromic deafness 96
-
Aliases:
-
DFNB96
-
autosomal recessive deafness 96
|
|
|
Homo sapiens (human)
|
|
DOID:0070120
|
-
Meckel syndrome 6
-
Aliases:
-
MKS6
-
Meckel-Gruber syndrome, type 6
|
|
|
Homo sapiens (human)
|
|
DOID:5165
|
-
uterine corpus sarcoma
-
Aliases:
-
sarcoma of Corpus Uteri
-
sarcoma of uterus
|
|
|
Homo sapiens (human)
|
|
DOID:0110778
|
-
hereditary spastic paraplegia 27
-
Aliases:
-
SPG27
-
autosomal recessive spastic paraplegia 27
-
autosomal recessive spastic paraplegia type 27
|
|
|
Homo sapiens (human)
|
|
DOID:0110294
|
-
autosomal recessive limb-girdle muscular dystrophy type 2T
-
Aliases:
-
LGMD2T
-
MDDGC14
-
muscular dystrophy limb-girdle type 2T
-
muscular dystrophy-dystroglycanopathy (limb-girdle) type C14
-
muscular dystrophy-dystroglycanopathy limb-girdle GMPPB-related
|
|
|
Homo sapiens (human)
|
|
DOID:0050778
|
|
|
|
Homo sapiens (human)
|
|
DOID:13911
|
|
|
|
Homo sapiens (human)
|
|
DOID:1751
|
-
malignant conjunctival melanoma
-
Aliases:
-
Conjunctival melanoma
-
malignant melanoma of conjunctiva
|
|
|
Homo sapiens (human)
|
|
DOID:9476
|
-
Sheehan syndrome
-
Aliases:
-
Postpartum Hypopituitarism
-
Sheehan's syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:0110477
|
-
autosomal recessive nonsyndromic deafness 2
-
Aliases:
-
DFNB2
-
autosomal recessive deafness 2
|
|
|
Homo sapiens (human)
|
|
DOID:4468
|
-
clear cell adenocarcinoma
-
Aliases:
-
Mesonephroid Clear cell carcinoma
-
Mesonephroma, malignant
-
Water-clear cell adenocarcinoma
-
Water-clear cell carcinoma
-
Wolffian duct neoplasm
-
malignant Mesonephroma
-
mesonephroma
|
|
|
Homo sapiens (human)
|
|
DOID:4362
|
-
cervical cancer
-
Aliases:
-
cervical neoplasm
-
cervix cancer
-
cervix uteri cancer
-
neoplasm of uterine cervix
-
tumor of the Cervix Uteri
-
uterine cervical neoplasm
|
|
|
Homo sapiens (human)
|
|
DOID:2444
|
|
|
|
Homo sapiens (human)
|
|
DOID:0110480
|
-
autosomal recessive nonsyndromic deafness 22
-
Aliases:
-
DFNB22
-
autosomal recessive deafness 22
|
|
|
Homo sapiens (human)
|
|