Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
angioimmunoblastic T-cell lymphoma	DOID_0111147	[A peripheral T-cell lymphoma characterized by autoimmune features and poor prognosis.]
glanders	DOID_13444	[A primary bacterial infectious disease that results in septicemic infection, has_material_basis_in Burkholderia mallei, which is transmitted by contact with tissues or body fluids of infected animals, or through mucosal surfaces such as the eyes and nose. The infection has symptom fever, has symptom chills, has symptom sweating, has symptom muscle aches, has symptom chest pain, has symptom muscle tightness, has symptom headache, has symptom mucopurulent nasal discharge, and has symptom nodular lesions in the lungs.]
obsolete nerve deafness	DOID_12113
ureteropelvic junction obstruction	DOID_0111145	[A urinary tract obstruction characterized by a blockage at the renal pelvis where the kidney attaches to the ureter.]
cartilage-hair hypoplasia	DOID_14773	[An ectodermal dysplasia characterized by short-limbed short stature and fine, sparse hair that has_material_basis_in homozygous or compound heterozygous mutation in RMRP on chromosome 9p13.3.]
acquired von Willebrand syndrome	DOID_0111146	[A blood coagulation disease characterized by development of a defect in clotting in the absence of previous bleeding symptoms, negative familial history, and occurrence in a relatively older age. Typically this develops secondarily to other disorders, such as lymphoproliferative, myeloproliferative, cardiovascular and autoimmune disorders.]
Rhinocladiella mackenziei	NCBITaxon_86056
gonococcal bursitis	DOID_13453
obsolete secondary syphilitic periostitis	DOID_12121
scleritis	DOID_13452
pulmonary alveolar proteinosis	DOID_12120	[A lung disease that is characterized by abnormal accumulation of surfactant occurs within the alveoli, interfering with gas exchange.]
obsolete Fryns syndrome	DOID_14787
coccidioidomycosis	DOID_13450	[A primary systemic mycosis that results_in systemic fungal infection, has_material_basis_in Coccidioides immitis, transmitted_by airborne spores and has_symptom conjunctivitis, has_symptom arthritis, has_symptom chest pain and results_in_formation_of skin nodules.]
spondyloepiphyseal dysplasia congenita	DOID_14789
autosomal dominant sensory ataxia 1	DOID_0111170	[A hereditary ataxia characterized by gait difficulty and instability especially in dark conditions resulting from sensory loss in the extremities and without cerebellar involvement that has_material_basis_in heterozygous mutations in the RNF170 gene on chromosome 8.]
hereditary ataxia	DOID_0050951	[A neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements.]
bulimia nervosa	DOID_12129	[An eating disorder characterized by the restraining of food intake for a period of time followed by an over intake or binging period that results in feelings of guilt and low self-esteem.]
obsolete secondary syphilitic hepatitis	DOID_13459	[A secondary syphilis that involves infection of the liver by the spirochete Treponema pallidum, which results in the formation of hepatic lesions.]
pica disease	DOID_12128	[An eating disorder that is characterized by an appetite for non-nutritive substances or food ingredients.]
KBG syndrome	DOID_14780	[A syndrome that is characterized by short stature, moderate to severe degrees of mental retardation, developmental abnormalities of the limbs, bones of the spine (vertebrae), extremities, and/or underdevelopment of the bones of the skeleton.]