Terminology Service < Semantic Lookup Platform

All terms in HP

Label	Id	Description
Megaloblastic erythroid hyperplasia	HP_0200143
brainstem motor neuron	CL_2000047	[Any motor neuron that is part of a brainstem.]
Abnormal liver function tests during pregnancy	HP_0200148
ventricular cardiac muscle cell	CL_2000046	[Any cardiac muscle cell that is part of a cardiac ventricle.]
obsolete Anaphylactoid purpura	HP_0200144
embryonic fibroblast	CL_2000042	[Any fibroblast that is part of a embryo.]
Neuronal loss in basal ganglia	HP_0200147	[A reduction in the number of nerve cells in the basal ganglia.]
Unilateral brachydactyly	HP_0006008
Gonadal dysgenesis, male	HP_0008668	[Unusual gonadal development in a person with a 46,XY male karyotype, leading to an unassigned sex differentiation.]
Hypotrophy of the small hand muscles	HP_0006006
Impaired histidine renal tubular absorption	HP_0008666
Clitoral hypertrophy	HP_0008665	[Hypertrophy of the clitoris.]
Urethral sphincter sclerosis	HP_0008664
Renal sarcoma	HP_0008663	[A sarcoma of the kidney.]
Renotubular dysgenesis	HP_0008660	[A developmental defect characterized by absence or poor development of proximal renal tubules.]
Bilateral choanal atresia/stenosis	HP_0200138
Bilateral choanal atresia	HP_0004502	[Bilateral absence (atresia) of the posterior nasal aperture (choana).]
Epileptic encephalopathy	HP_0200134	[A condition in which epileptiform abnormalities are believed to contribute to the progressive disturbance in cerebral function. Epileptic encephalaopathy is characterized by (1) electrographic EEG paroxysmal activity that is often aggressive, (2) seizures that are usually multiform and intractable, (3) cognitive, behavioral and neurological deficits that may be relentless, and (4) sometimes early death.]
Lumbosacral meningocele	HP_0200133
splenic endothelial cell	CL_2000053	[Any endothelial cell that is part of a spleen.]