DOID:1074
|
|
|
|
Rattus norvegicus (Norway rat)
|
DOID:1678
|
-
chronic interstitial cystitis
|
|
|
Homo sapiens (human)
|
DOID:2660
|
|
|
|
Homo sapiens (human)
|
DOID:5289
|
-
uterus leiomyosarcoma
-
Aliases:
-
leiomyosarcoma of Corpus Uteri
|
|
|
Homo sapiens (human)
|
DOID:11723
|
-
Duchenne muscular dystrophy
-
Aliases:
-
Muscular dystrophy, Duchenne
|
|
|
Homo sapiens (human)
|
DOID:6576
|
-
childhood optic nerve glioma
-
Aliases:
-
glioma of the pediatric visual pathway
|
|
|
Homo sapiens (human)
|
DOID:11111
|
|
|
|
Homo sapiens (human)
|
DOID:8778
|
-
Crohn's disease
-
Aliases:
-
Crohn disease
-
Crohn's disease of colon
-
Crohn's disease of large bowel
-
Granulomatous Colitis
-
Pediatric Crohn's disease
|
|
|
Danio rerio (zebrafish)
|
DOID:0110004
|
-
3-methylglutaconic aciduria type 3
-
Aliases:
-
3-methylglutaconic aciduria type III
-
Costeff optic atrophy syndrome
-
Costeff syndrome
-
Iraqi-Jewish optic atrophy plus
-
MGA3
-
autosomal recessive optic atrophy plus syndrome
-
autosomal recessive optic atrophy type 3
-
infantile optic atrophy with chorea and spastic paraplegia
|
|
|
Homo sapiens (human)
|
DOID:2741
|
-
bilirubin metabolic disorder
-
Aliases:
-
hereditary hyperbilirubinemia
-
hyperbilirubinemia
|
|
|
Xenopus tropicalis (tropical clawed frog)
|
DOID:11724
|
-
limb-girdle muscular dystrophy
-
Aliases:
-
Erb's muscular dystrophy
-
Leyden-Mbius muscular dystrophy
-
limb girdle muscular dystrophy
|
|
|
Rattus norvegicus (Norway rat)
|
DOID:0050012
|
|
|
|
Homo sapiens (human)
|
DOID:0070218
|
-
familial hyperinsulinemic hypoglycemia 2
-
Aliases:
-
Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency
-
HHF2
-
hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia
|
|
|
Rattus norvegicus (Norway rat)
|
DOID:0090090
|
-
hypogonadotropic hypogonadism 19 with or without anosmia
|
|
|
Homo sapiens (human)
|
DOID:0060295
|
-
complement component 2 deficiency
|
|
|
Homo sapiens (human)
|
DOID:9408
|
-
acute myocardial infarction
|
|
|
Rattus norvegicus (Norway rat)
|
DOID:0060706
|
-
X-linked lymphoproliferative syndrome 2
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0110801
|
-
hereditary spastic paraplegia 49
-
Aliases:
-
SPG49
-
autosomal recessive spastic paraplegia 49
-
autosomal recessive spastic paraplegia type 49
|
|
|
Homo sapiens (human)
|
DOID:9854
|
-
lingual-facial-buccal dyskinesia
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:2237
|
-
hepatitis
-
Aliases:
-
acute and subacute liver necrosis
-
acute hepatitis
-
acute/subac. necrosis of liver
-
animal hepatitis
-
chronic hepatitis
-
chronic persistent hepatitis
|
|
|
Rattus norvegicus (Norway rat)
|
DOID:705
|
-
Leber hereditary optic neuropathy
-
Aliases:
-
Leber's hereditary optic neuropathy
-
Leber's optic atrophy
|
|
|
Mus musculus (house mouse)
|
DOID:0060284
|
-
paroxysmal nocturnal hemoglobinuria
|
|
|
Mus musculus (house mouse)
|
DOID:0110113
|
-
atrial heart septal defect 8
-
Aliases:
-
ASD8
-
atrial septal defect 8
|
|
|
Homo sapiens (human)
|
DOID:0110282
|
-
autosomal recessive limb-girdle muscular dystrophy type 2H
-
Aliases:
-
LGMD2H
-
limb-girdle muscular dystrophy due to TRIM32 deficiency
-
muscular dystrophy Hutterite type
-
sarcotubular myopathy
|
|
|
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)
|