Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
obsolete Pars plana primary cyst	DOID_11145
pes anserinus tendinitis or bursitis	DOID_12475
Charcot-Marie-Tooth disease axonal type 2V	DOID_0110178	[A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NAGLU gene on chromosome 17q21.]
miliaria rubra	DOID_11153	[A miliaria that is characterized by erythematous papules resulting in leakage of sweat into the deeper, subcorneal layers of the epidermis provoking a local inflammatory reaction.]
cholecystolithiasis	DOID_11151
obsolete glaucoma due to raised episcleral venous pressure	DOID_11150
developing anatomical structure	UBERON_0005423
obsolete disorder of optic chiasm associated with non-pituitary neoplasm	DOID_11158
hypohidrosis	DOID_11155	[A sweat gland disease that is characterized by reduced ability to sweat, has_symptom hyperthermia and dry skin of affected areas, and has_material_basis_in trauma to the sweat glands.]
chief cell of parathyroid gland	CL_0000446
epithelial cell of parathyroid gland	CL_0002260
band keratopathy	DOID_11164
Charcot-Marie-Tooth disease dominant intermediate B	DOID_0110197	[A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in mutation in the gene encoding dynamin-2 (DNM2).]
common wart	DOID_11165	[A viral infectious disease that results_in infection located_in skin, has_material_basis_in human papillomavirus (types 2 and 4). This infection has_symptom raised wart with roughened surface, most common on hands, but can grow anywhere on the body.]
anterior spinal artery	UBERON_0005431
Charcot-Marie-Tooth disease recessive intermediate C	DOID_0110198	[A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in homozygous or compound heterozygous mutation in the PLEKHG5 gene on chromosome 1p36.]
Charcot-Marie-Tooth disease type 4E	DOID_0110195	[A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or heterozygous mutation in the EGR2 gene on chromosome 10q21 or by heterozygous mutation in the MPZ gene on chromosome 1q23.]
obsolete apnea of prematurity	DOID_11163
Charcot-Marie-Tooth disease type 4G	DOID_0110196	[A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the HK1 gene on chromosome 10q22.]
Charcot-Marie-Tooth disease type 4F	DOID_0110193	[A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the periaxin gene (PRX) on chromosome 19q13.]