Terminology Service < Semantic Lookup Platform

All terms in HP

Label	Id	Description
Exostoses of hand bones	HP_0004276	[Abnormal formation of new bone on the surface of a bone of the hand.]
Cortical thickening of hand bones	HP_0004271
Cupped metaphyses of hand bones	HP_0004273
Cortical thinning of hand bones	HP_0004272
Irregular ossification of hand bones	HP_0004280
Increased urine urobilinogen	HP_0031890	[An elevated concentration of urobilinogen in the urine.]
Decreased eosinophil count	HP_0031891	[Abnormal reduction in the count of eosinophils in the blood per volume.]
Sclerotic foci in hand bones	HP_0004289
Irregular sclerosis of hand bones	HP_0004281
Hyperglycorrhachia	HP_0031885	[Abnormally high glucose concentration in the cerebrospinal fluid.]
Overmodelled hand bones	HP_0004285
Pointed hand bones	HP_0004287
Notched hand bones	HP_0004284
Narrow palm	HP_0004283	[For children from birth to 4 years of age, the palm width is more than 2 SD below the mean; for children from 4 to 16 years of age the palm width is below the 5th centile; or, the width of the palm appears disproportionately narrow for its length.]
Stippled calcification of hand bones	HP_0004291
Sclerosis of hand bones with transverse striations	HP_0004290
Increased proinsulin:insulin ratio	HP_0031883	[An elevated concentration of proinsulin (the prohormone precursor to insulin) to mature insulin in the circulation.]
Decreased tear drainage	HP_0031881	[A form of watery eye associated with obstruction of the nasolacrimal system. This may arise at the level of the punctum, the canaliculi, the sac or the nasolacrimal duct.]
Agyria	HP_0031882	[A congenital abnormality of the cerebral hemisphere characterized by lack of gyrations (convolutions) of the cerebral cortex. Agyria is defined as cortical regions lacking gyration with sulci great than 3 cm apart and cerebral cortex thicker than 5 mm.]
cortex of manus bone	UBERON_0005809	[The outer or sperficial part of a bone of the manus.]