DOID:308
|
-
early myoclonic encephalopathy
-
Aliases:
-
Epileptic seizures - myoclonic
-
Epileptic seizures, myoclonic
-
Myoclonic seizure
-
Myoclonic seizure disorder
-
myoclonia epileptica
-
myoclonic epilepsy
|
|
|
Homo sapiens (human)
|
|
DOID:2960
|
-
photosensitive trichothiodystrophy
-
Aliases:
-
IBIDS syndrome
-
TTD-P
-
Tay syndrome
-
sulfur-deficient brittle hair syndrome
-
trichothiodystrophy with congenital ichthyosis
|
|
|
Homo sapiens (human)
|
|
DOID:10983
|
|
|
|
Homo sapiens (human)
|
|
DOID:986
|
|
|
|
Homo sapiens (human)
|
|
DOID:4329
|
|
|
|
Homo sapiens (human)
|
|
DOID:0060735
|
-
epidermolysis bullosa simplex Dowling-Meara type
-
Aliases:
-
EBS-gen sev
-
EBSDM
-
epidermolysis bullosa herpetiformis Dowling-Meara type
-
epidermolysis bullosa simplex, herpetiformis
-
generalized severe epidermolysis bullosa simplex
|
|
|
Homo sapiens (human)
|
|
DOID:0060312
|
-
angular cheilitis
-
Aliases:
-
angular cheilosis
-
angular stomatitis
-
cheilosis
-
commissural cheilitis
|
|
|
Homo sapiens (human)
|
|
DOID:0050636
|
-
familial visceral amyloidosis
-
Aliases:
-
AMYLOIDOSIS, FAMILIAL RENAL
-
German type amyloidosis
-
OSTERTAG TYPE AMYLOIDOSIS
-
systemic nonneuropathic amyloidosis
|
|
|
Homo sapiens (human)
|
|
DOID:5268
|
|
|
|
Homo sapiens (human)
|
|
DOID:0110562
|
-
autosomal dominant nonsyndromic deafness 33
-
Aliases:
-
DFNA33
-
autosomal dominant deafness 33
|
|
|
Homo sapiens (human)
|
|
DOID:6367
|
-
acral lentiginous melanoma
-
Aliases:
-
acral lentiginous melanoma, malignant
-
malignant acral lentiginous melanoma
|
|
|
Homo sapiens (human)
|
|
DOID:0060730
|
-
torsion dystonia 1
-
Aliases:
-
dystonia musculorum deformans
|
|
|
Homo sapiens (human)
|
|
DOID:8717
|
-
decubitus ulcer
-
Aliases:
-
Decubitus (pressure) ulcer
-
Decubitus ulcer any site
-
pressure sores
-
pressure ulcer
|
|
|
Homo sapiens (human)
|
|
DOID:9562
|
-
primary ciliary dyskinesia
-
Aliases:
-
ciliary motility disorder
-
immotile ciliary syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:0060857
|
-
septooptic dysplasia
-
Aliases:
-
De Morsier syndrome
-
SOD
-
septo-optic dysplasia
|
|
|
Homo sapiens (human)
|
|
DOID:4235
|
|
|
|
Homo sapiens (human)
|
|
DOID:0060770
|
-
dextro-looped transposition of the great arteries
-
Aliases:
-
D-TGA
-
DTGA1
-
congenitally uncorrected transposition of the great arteries
-
congenitally uncorrected transposition of the great vessels
-
isolated ventriculoarterial discordance
-
ventriculoarterial discordance with atrioventricular concordance
|
|
|
Homo sapiens (human)
|
|
DOID:12930
|
-
dilated cardiomyopathy
-
Aliases:
-
primary dilated cardiomyopathy
|
|
|
Homo sapiens (human)
|
|
DOID:12450
|
|
|
|
Homo sapiens (human)
|
|
DOID:1618
|
-
breast fibroadenoma
-
Aliases:
-
Complex Fibroadenoma of breast
-
Fibroadenoma of breast
-
Juvenile fibroadenoma
-
cellular Fibroadenoma
-
fibroadenoma
-
juvenile fibroadenoma of breast
|
|
|
Homo sapiens (human)
|
|
DOID:0080326
|
-
familial hypertrophic cardiomyopathy
|
|
|
Homo sapiens (human)
|
|
DOID:7997
|
|
|
|
Homo sapiens (human)
|
|
DOID:0060768
|
-
Smith-Magenis syndrome
-
Aliases:
-
17p11.2 microdeletion syndrome
-
chromosome 17p11.2 deletion syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:0080479
|
-
peroxisome biogenesis disorder 4A
-
Aliases:
-
peroxisome biogenesis disorder 4A (Zellweger)
|
|
|
Homo sapiens (human)
|
|
DOID:2548
|
-
reflex epilepsy
-
Aliases:
-
epilepsy, sensory-induced
|
|
|
Homo sapiens (human)
|
|