Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
autosomal recessive nonsyndromic deafness 63	DOID_0110515	[An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the LRTOMT gene on chromosome 11q13.]
autosomal recessive nonsyndromic deafness 65	DOID_0110516	[An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 20q13.2-q13.3.]
obsolete bone marrow tansplantation nephropathy	DOID_2980
obsolete commensal Fusobacteriaceae infectious disease	DOID_0050368
kidney papillary necrosis	DOID_2981
obsolete Myroides odoratus necrotizing fasciitis	DOID_0050367
perinephritis	DOID_2982
anuria	DOID_2983
obsolete primary Mycoplasmataceae infectious disease	DOID_0050369
obsolete chronic rejection of renal transplant	DOID_2985
heart septal defect	DOID_1681
familial Mediterranean fever	DOID_2987	[An autoimmune hypersensitivity disease characterized by recurrent episodes of fever and acute inflammation of the membranes lining the abdomen, joints and lungs; that has_material_basis_in mutations in the MEFV gene, which encodes the protein pyrin.]
breast leiomyoma	DOID_1623	[A breast benign neoplasm that has_material_basis in smooth muscle cells.]
obsolete intra-abdominal lymphangioma	DOID_2956
pulmonary tuberculosis	DOID_2957	[A tuberculosis that is a contagious disease located_in lungs. The infection has_symptom fever, has_symptom cough, has_symptom difficulty in breathing, has_symptom inflammatory infiltrations, has_symptom formation of tubercles, has_symptom caseation, has_symptom pleural effusion, and has_symptom fibrosis.]
obsolete environmental illness	DOID_2958
obsolete breast fibroepithelial tumor	DOID_1620
obsolete primary Helicobacteraceae infectious disease	DOID_0050311
obsolete primary Listeriaceae infectious disease	DOID_0050310
autosomal dominant nonsyndromic deafness 15	DOID_0110546	[An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the POU4F3 gene on chromosome 5q32.]