Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
Viridiplantae	NCBITaxon_33090
right lower quadrant abdominal tenderness	SYMP_0000500
familial hyperinsulinemic hypoglycemia 1	DOID_0070219	[A hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of hyperinsulinemic hypoglycemia that is resistant to diazoxide treatment that has_material_basis_in mutation in the ABCC8 gene on chromosome 11p15.]
generalized abdominal pain	SYMP_0000518
oxoacid derivative	CHEBI_33241
sulfur molecular entity	CHEBI_26835
abnormal feces	SYMP_0000519
lump in chest	SYMP_0000516
hemoptysis	SYMP_0000517	[Hemoptysis is a respiratory system and chest symptom characterized by an expectoration of blood from some part of the respiratory tract.]
hiccough	SYMP_0000515	[Hiccough is a respiratory system and chest symptom characterized by a spasmodic inhalation with closure of the glottis accompanied by a peculiar sound.]
male stress incontinence	SYMP_0000512
stress incontinence	SYMP_0000853	[Stress incontinence is a urinary incontinence characterized by an involuntary leakage of urine from the bladder accompanying physical activity (as in laughing, coughing, sneezing, or physical exercise) which places increased pressure on the abdomen.]
stridor	SYMP_0000513	[Stridor is a respiratory system and chest symptom characterized by a harsh vibrating sound heard during respiration in cases of obstruction of the air passages.]
Parkinson's disease 4	DOID_0060895	[A late onset Parkinson disease that has_material_basis_in heterozygous triplication of the alpha-synuclein gene on chromosome 4q22.]
late onset Parkinson's disease	DOID_0060892	[A Parkinson's disease characterized by onset of motor symptoms typically after 60 years of age.]
Parkinson's disease 23	DOID_0060896	[An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22.]
Parkinson's disease 17	DOID_0060897	[A late-onset Parkinson disease that has_material_basis_in heterozygous mutation in the VPS35 gene on chromosome 16q13.]
Parkinson's disease 20	DOID_0060898	[An early-onset Parkinson disease that has_material_basis_in homozygous mutation in the SYNJ1 gene on chromosome 21q22.]
ectopic Cushing syndrome	DOID_0060890	[A primary hyperaldosteronism that is characterized by a tumor outside the pituitary gland produces a hormone called adrenocorticotropic hormone.]
primary hyperaldosteronism	DOID_446	[An adrenal gland hyperfunction disease that results in the overproduction of aldosterone by the adrenal glands.]