DOID:9778
|
-
irritable bowel syndrome
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:3877
|
-
functional colonic disease
|
|
|
Homo sapiens (human)
|
|
DOID:12918
|
-
thromboangiitis obliterans
-
Aliases:
-
Buerger's disease
-
Presenile gangrene
|
|
|
Homo sapiens (human)
|
|
DOID:0110337
|
-
osteogenesis imperfecta type 7
-
Aliases:
-
OI7
-
osteogenesis imperfecta type VII
|
|
|
Homo sapiens (human)
|
|
DOID:0050861
|
-
colorectal adenocarcinoma
|
|
|
Homo sapiens (human)
|
|
DOID:7474
|
-
malignant pleural mesothelioma
-
Aliases:
-
malignant mesothelioma of pleura
|
|
|
Homo sapiens (human)
|
|
DOID:7148
|
-
rheumatoid arthritis
-
Aliases:
-
Arthritis or polyarthritis, rheumatic
-
atrophic Arthritis
|
|
|
Homo sapiens (human)
|
|
DOID:934
|
-
viral infectious disease
-
Aliases:
-
Viral Infection
-
Viral disease
-
virus infection
|
|
|
Homo sapiens (human)
|
|
DOID:2256
|
-
osteochondrodysplasia
-
Aliases:
-
Cartilage Development disorder
-
Congenital anomaly of cartilage
-
Osteochondrodysplasia syndrome
-
chondrodystrophy
-
skeletal dysplasia
|
|
|
Homo sapiens (human)
|
|
DOID:10871
|
-
age related macular degeneration
-
Aliases:
-
Age Related Maculopathies
-
Age Related Maculopathy
-
Senile macular degeneration
-
Senile macular retinal degeneration
-
age-related macular degeneration
|
|
|
Homo sapiens (human)
|
|
DOID:10595
|
-
Charcot-Marie-Tooth disease
-
Aliases:
-
CMT - Charcot-Marie-Tooth disease
|
|
|
Homo sapiens (human)
|
|
DOID:3144
|
|
|
|
Homo sapiens (human)
|
|
DOID:0070135
|
-
autosomal recessive cutis laxa type IA
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:0070136
|
-
autosomal dominant cutis laxa 2
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:3534
|
-
Lafora disease
-
Aliases:
-
Lafora Progressive Myoclonic Epilepsy
-
Lafora's disease
-
MYOCLONIC EPILEPSY OF LAFORA
|
|
|
Mus musculus (house mouse)
|
|
DOID:0060611
|
-
abdominal obesity-metabolic syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:0070054
|
-
Vulto-van Silfout-de Vries syndrome
-
Aliases:
-
IDDISBAS
-
MRD24
-
VSVS
-
autosomal dominant mental retardation 24
-
autosomal dominant non-syndromic intellectual disability 24
-
intellectual developmental disorder with impaired expressive speech and behavioral abnormalities, with or without seizures
|
|
|
Homo sapiens (human)
|
|
DOID:0111974
|
-
immunodeficiency 59
-
Aliases:
-
IMD59
-
granulocytopenia with immunoglobin abnormality
-
immunodeficiency 59 and hypoglycemia
|
|
|
Homo sapiens (human)
|
|
DOID:0050983
|
-
spinocerebellar ataxia type 36
|
|
|
Homo sapiens (human)
|
|
DOID:0050951
|
|
|
|
Homo sapiens (human)
|
|
DOID:9277
|
-
primary cerebellar degeneration
|
|
|
Homo sapiens (human)
|
|
DOID:0070411
|
-
autosomal recessive spinocerebellar ataxia 30
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:5082
|
-
liver cirrhosis
-
Aliases:
-
Cirrhosis
-
cirrhosis of liver
|
|
|
Mus musculus (house mouse)
|
|
DOID:2237
|
-
hepatitis
-
Aliases:
-
acute and subacute liver necrosis
-
acute hepatitis
-
acute/subac. necrosis of liver
-
animal hepatitis
-
chronic hepatitis
-
chronic persistent hepatitis
|
|
|
Mus musculus (house mouse)
|
|
DOID:12365
|
|
|
|
Homo sapiens (human)
|
|