Terminology Service < Semantic Lookup Platform

All terms in HP

Label	Id	Description
accessory ciliary ganglion	UBERON_0035776	[A parasympathetic ganglion located on the short ciliary nerve differentiated from the main ciliary ganglion by virtue of the fact that it had no root derived directly from the inferior trunk of the oculomotor nerve and it never attaches to this nerve]
regulation of chromosome organization	GO_0033044	[Any process that modulates the frequency, rate or extent of a process involved in the formation, arrangement of constituent parts, or disassembly of a chromosome.]
negative regulation of sister chromatid segregation	GO_0033046	[Any process that stops, prevents, or reduces the frequency, rate or extent of sister chromatid segregation.]
regulation of sister chromatid segregation	GO_0033045	[Any process that modulates the frequency, rate or extent of sister chromatid segregation.]
regulation of mitotic sister chromatid segregation	GO_0033047	[Any process that modulates the frequency, rate or extent of sister chromatid segregation during mitosis.]
regulation of microtubule-based movement	GO_0060632	[Any process that modulates the rate, frequency, or extent of microtubule-based movement, the movement of organelles, other microtubules and other particles along microtubules, mediated by motor proteins.]
Nasal regurgitation	HP_0011469	[Regurgitation of milk through the nose.]
Childhood onset	HP_0011463	[Onset of disease at the age of between 1 and 5 years.]
Aganglionosis of the small intestine	HP_0011464	[A lack of intestinal ganglion cells (i.e., an aganglionic section of bowel) affecting the small intestine.]
toxin	CHEBI_27026	[Poisonous substance produced by a biological organism such as a microbe, animal or plant.]
Fetal onset	HP_0011461	[Onset prior to birth but after 8 weeks of gestation.]
Young adult onset	HP_0011462	[Onset of disease at the age of between 16 and 40 years.]
Absent gallbladder	HP_0011467	[A developmental defect in which the gallbladder fails to form.]
Facial tics	HP_0011468	[Sudden, repetitive, nonrhythmic motor movements (spasms), involving the eyes and muscles of the face.]
glycine transporter inhibitor	CHEBI_85425	[Any substance that inhibits the action of glycine transporters.]
Duodenal aganglionosis	HP_0011465	[A lack of intestinal ganglion cells (i.e., an aganglionic section of bowel) affecting the duodenum.]
Embryonal onset	HP_0011460	[Onset of disease at up to 8 weeks of gestation.]
EC 2.1.2.1 (glycine hydroxymethyltransferase) inhibitor	CHEBI_64570	[An EC 2.1.2.* (hydroxymethyl-, formyl- and related transferases) inhibitor that interferes with the action of glycine hydroxymethyltransferase (EC 2.1.2.1).]
Persistent stapedial artery	HP_0011475	[Persistence of the stapedial artery, which normally regresses during embryonic life.]
Abnormality of small intestinal villus morphology	HP_0011472