Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
Phthiraptera	NCBITaxon_85819
Psocodea	NCBITaxon_1930602
synovitis	SYMP_0000646	[Synovitis is a joint inflammation characterized by an inflammation of a synovial membrane usually with pain and swelling of the joint.]
joint inflammation	SYMP_0000313
sulfonic acid derivative	CHEBI_33552
sulfur oxoacid derivative	CHEBI_33424
tache noire	SYMP_0000647	[Tache noire is a skin ulcer characterized by a small dark-centered ulcer that appears at the site of a tick bite and is the primary lesion of boutonneuse fever.]
ruffled feather	SYMP_0000644
Miura type epiphyseal chondrodysplasia	DOID_0070316	[A bone developmental disease characterized by tall stature, scoliosis and macrodactyly of the great toes that has_material_basis_in heterozygous mutation in the NPR2 gene on chromosome 9p13.]
bone development disease	DOID_0080006	[A bone disease that results_in abnormal growth and development located_in bone or located_in cartilage.]
wet beriberi	DOID_0070317	[A beriberi that is located_in the cardiovascular system and has_symptom increased heart rate, swelling of lower legs, and shortness of breath.]
beriberi	DOID_13725	[A thiamine deficiency disease that is characterized by being severe and chronic.]
obstructive nephropathy	DOID_0070314	[A kidney disease characterized by kidney damage and dysfunction resulting from urinary tract obstruction.]
hypoplastic right heart syndrome	DOID_0070315	[A congenital heart disease characterized by underdevelopment of the structures on the right side of the heart commonly associated with atrial septal defect.]
obsolete Peters-Plus Syndrome	DOID_0070312	[A syndrome that is characterized by anterior chamber eye anomalies, short limbs with broad distal extremities, characteristic facial features, cleft lip or palate, and variable developmental delay or intellectual disability.]
nutritional deficiency disease	DOID_5113	[A nutrition disease that is characterized by deficiency of a nutritional element, such as a vitamin, mineral, carbohydrate, protein, fat, or general energy content.]
drug-induced hearing loss	DOID_0070310	[A nonsyndromic deafness that is characterized by cochlear or vestibular dysfunction resulting in loss of hearing caused by drug ototoxicity.]
nonsyndromic deafness	DOID_0050563	[An auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms.]
oligoasthenoteratozoospermia	DOID_0070311	[A form of male infertility that is characterized by a combination of low number or oligozoospermia, poor motility or asthenozoospermia, and abnormal shape or teratozoospermia of sperms. OAT is the most common cause of male subfertility.]
respiratory failure	SYMP_0000643