DOID:9993
|
|
|
|
Homo sapiens (human)
|
|
DOID:0080568
|
-
congenital disorder of glycosylation Iq
-
Aliases:
-
congenital disorder of glycosylation 1q
|
|
|
Homo sapiens (human)
|
|
DOID:4647
|
-
trilateral retinoblastoma
|
|
|
Homo sapiens (human)
|
|
DOID:0070432
|
-
hyperphosphatasia with impaired intellectual development syndrome 5
-
Aliases:
-
GPIBD11
-
HPMRS5
-
glycosylphosphatidylinositol biosynthesis defect 11
-
hyperphosphatasia with mental retardation syndrome 5
|
|
|
Homo sapiens (human)
|
|
DOID:2058
|
-
chronic mucocutaneous candidiasis
|
|
|
Homo sapiens (human)
|
|
DOID:0110515
|
-
autosomal recessive nonsyndromic deafness 63
-
Aliases:
-
DFNB63
-
autosomal recessive deafness 63
|
|
|
Homo sapiens (human)
|
|
DOID:4248
|
-
coronary stenosis
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:12594
|
-
Potter's syndrome
-
Aliases:
-
Potter sequence
-
Potter syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:0110445
|
-
dilated cardiomyopathy 1KK
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:3451
|
|
|
|
Homo sapiens (human)
|
|
DOID:0060248
|
-
Simpson-Golabi-Behmel syndrome type 1
-
Aliases:
-
DGSX Golabi-Rosen syndrome
-
Golabi-Rosen syndrome
-
SGB syndrome
-
Sara Angers syndrome
-
Simpson dysmorphia syndrome
-
X-linked dysplasia gigantism syndrome
-
bulldog syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:0110107
|
-
atrial heart septal defect 2
-
Aliases:
-
ASD2
-
atrial septal defect 2
|
|
|
Homo sapiens (human)
|
|
DOID:0050523
|
-
adult T-cell leukemia/lymphoma
-
Aliases:
-
Adult T-cell leukemia/lymphoma (HTLV-1 positive)
-
adult T-cell leukemia
|
|
|
Homo sapiens (human)
|
|
DOID:4677
|
|
|
|
Homo sapiens (human)
|
|
DOID:0110131
|
-
Bardet-Biedl syndrome 9
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:11249
|
-
vitamin K deficiency bleeding
-
Aliases:
-
deficiency of vitamin K
-
vitamin K deficiency
-
vitamin K deficiency hemorrhagic disease
|
|
|
Homo sapiens (human)
|
|
DOID:10314
|
|
|
|
Homo sapiens (human)
|
|
DOID:1405
|
-
primary angle-closure glaucoma
-
Aliases:
-
primary Angle Closure Glaucoma
|
|
|
Homo sapiens (human)
|
|
DOID:203
|
-
exostosis
-
Aliases:
-
bone spur
-
bony outgrowth
-
orbital exostosis
-
osteophyte
-
swimmer's exostosis
|
|
|
Homo sapiens (human)
|
|
DOID:0111672
|
-
primary hyperoxaluria type 3
-
Aliases:
-
HP3
-
PH III
-
primary hyperoxaluria type III
|
|
|
Homo sapiens (human)
|
|
DOID:12733
|
|
|
|
Homo sapiens (human)
|
|
DOID:12139
|
-
dysthymic disorder
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:0110467
|
-
autosomal recessive nonsyndromic deafness 12
-
Aliases:
-
DFNB12
-
autosomal recessive deafness 12
|
|
|
Homo sapiens (human)
|
|
DOID:0050566
|
-
X-linked nonsyndromic deafness
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:11396
|
|
|
|
Homo sapiens (human)
|
|