DOID:14320
|
-
generalized anxiety disorder
|
|
|
Drosophila melanogaster (fruit fly)
|
|
DOID:10652
|
-
Alzheimer's disease
-
Aliases:
-
Alzheimer disease
-
Alzheimers dementia
|
|
|
Homo sapiens (human)
|
|
DOID:0080600
|
-
COVID-19
-
Aliases:
-
2019 Novel Coronavirus (2019-nCoV)
-
2019-nCoV infection
-
COVID19
-
SARS-CoV-2 infection
-
Wuhan coronavirus infection
-
Wuhan seafood market pneumonia virus infection
|
|
|
Homo sapiens (human)
|
|
DOID:2377
|
-
multiple sclerosis
-
Aliases:
-
Generalized multiple sclerosis
-
insular sclerosis
|
|
|
Homo sapiens (human)
|
|
DOID:14330
|
-
Parkinson's disease
-
Aliases:
-
Parkinson disease
-
paralysis agitans
|
|
|
Homo sapiens (human)
|
|
DOID:2320
|
-
obstructive lung disease
-
Aliases:
-
respiratory airway obstruction
|
|
|
Homo sapiens (human)
|
|
DOID:13208
|
-
background diabetic retinopathy
-
Aliases:
-
Non proliferative diabetic retinopathy
-
Non-Proliferative Diabetic Retinopathy
|
|
|
Homo sapiens (human)
|
|
DOID:10754
|
|
|
|
Homo sapiens (human)
|
|
DOID:14115
|
-
toxic shock syndrome
-
Aliases:
|
|
|
Rattus norvegicus (Norway rat)
|
|
DOID:583
|
-
hemolytic anemia
-
Aliases:
|
|
|
Rattus norvegicus (Norway rat)
|
|
DOID:9164
|
-
achalasia
-
Aliases:
-
Lack of reflex relaxation of lower oesophageal sphincter
-
achalasia of cardia
-
achalasia of esophagus
-
cardiospasm
-
esophageal achalasia
-
hypertensive lower esophageal sphincter
|
|
|
Homo sapiens (human)
|
|
DOID:0050602
|
-
triple-A syndrome
-
Aliases:
-
AAAS
-
Achalasia-Addisonianism-Alacrimia syndrome
-
Allgrove Syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:0111866
|
-
trichothiodystrophy
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:0080451
|
-
developmental and epileptic encephalopathy 29
-
Aliases:
-
DEE29
-
early infantile epileptic encephalopathy 29
|
|
|
Homo sapiens (human)
|
|
DOID:10579
|
|
|
|
Homo sapiens (human)
|
|
DOID:0110177
|
-
Charcot-Marie-Tooth disease axonal type 2N
-
Aliases:
-
CMT2N
-
Charcot-Marie-Tooth neuropathy axonal type 2N
-
autosomal dominant Charcot-Marie-Tooth disease type 2N
-
autosomal dominant axonal Charcot-Marie-Tooth disease type 2N
|
|
|
Homo sapiens (human)
|
|
DOID:0111479
|
-
combined oxidative phosphorylation deficiency 8
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:0070396
|
-
progressive leukoencephalopathy with ovarian failure
|
|
|
Homo sapiens (human)
|
|
DOID:12858
|
-
Huntington's disease
-
Aliases:
-
HD
-
Huntington disease
-
Huntington's chorea
|
|
|
Homo sapiens (human)
|
|
DOID:0060174
|
-
GABA aminotransferase deficiency
-
Aliases:
-
Gamma-amino butyric acid transaminase deficiency
-
gamma-aminobutyric acid transaminase deficiency
|
|
|
Homo sapiens (human)
|
|
DOID:9352
|
-
type 2 diabetes mellitus
-
Aliases:
-
NIDDM
-
insulin resistance
-
non-insulin-dependent diabetes mellitus
-
type 2 diabetes
-
type II diabetes mellitus
|
|
|
Homo sapiens (human)
|
|
DOID:3393
|
-
coronary artery disease
-
Aliases:
-
CHD
-
Coronary disease
-
coronary arteriosclerosis
-
coronary heart disease
|
|
|
Homo sapiens (human)
|
|
DOID:9970
|
|
|
|
Homo sapiens (human)
|
|
DOID:1387
|
-
hypolipoproteinemia
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:1388
|
-
Tangier disease
-
Aliases:
-
familial alpha-lipoprotein deficiency
-
familial high density lipoprotein deficiency
|
|
|
Homo sapiens (human)
|
|