Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
Archamoebae	NCBITaxon_555406
Parkinson's disease 19A	DOID_0060891	[An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31.]
juvenile-onset Parkinson's disease	DOID_0060893	[An early-onset Parkinson's disease that is characterized by onset of motor symptoms prior to 21 years of age.]
pallor	SYMP_0000510	[Pallor is a skin and integumentary tissue symptom characterized as a deficiency of color especially of the face.]
systemic vein	UBERON_0013140
flushing	SYMP_0000511	[Flushing is a skin and integumentary tissue symptom characterized as a markedly red flush in a persons face and often other areas of the skin, from various physiological conditions. Flushing is generally distinguished, despite a close physiological relation between them, from blushing, which is milder, generally restricted to the face or cheeks, and generally assumed to reflect embarrassment. Flushing is also a cardinal symptom of carcinoid syndrome the syndrome that results from hormones (often serotonin or histamine) being secreted into systemic circulation.]
paraurethral gland	UBERON_0010145
female reproductive gland	UBERON_0005398
male accessory sex gland	UBERON_0010147
male reproductive gland	UBERON_0005399
tachycardia	SYMP_0000529	[Tachycardia is a cardiovascular system symptom consisting of a relatively rapid heart action whether physiological (as after exercise) or pathological.]
arrhythmia	SYMP_0000287	[Arrhythmia is a cardiovascular system symptom consisting of an alteration in rhythm of the heartbeat either in time or force.]
undiagnosed cardiac murmur	SYMP_0000527
transient alteration of awareness	SYMP_0000525
ascites	SYMP_0000526	[An abdominal symptom consisting of an abnormal accumulation of serous fluid in the spaces between tissues and organs in the cavity of the abdomen.]
anorexia	SYMP_0000523	[Anorexia is a nutrition, metabolism, and development symptom characterized by a loss of appetite especially when prolonged.]
polyphagia	SYMP_0000524	[Polyphagia is a nutrition, metabolism, and development symptom characterized by an excessive appetite or eating.]
intestinal hypomagnesemia 1	DOID_0060883	[A hypomagnesemia characterized by very low serum magnesium levels due to defects in intestinal absorbtion and kidney excretion and secondary hypocalcemia that has material_basis_in homozygous or compound heterozygous mutations in the TRPM6 gene on chromosome 9q21.]
renal hypomagnesemia 6	DOID_0060884	[A hypomagnesemia characterized by autosomal dominant inheritance of severely lowered serum magnesium levels without other electrolyte disturbances or abnormalities in urinary magnesium excretion that has material_basis_in heterozygous mutation in the CNNM2 gene on chromosome 10q24.]
renal hypomagnesemia 2	DOID_0060885	[A hypomagnesemia characterized by autosomal dominant inheritance of hypomagnesemia due to renal magnesium loss that has material_basis_in heterozygous mutation in the FXYD2 gene on chromosome 11q23.]