Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
obsolete primary Thermomonosporaceae infectious disease	DOID_0050345
obsolete primary Streptomycetaceae infectious disease	DOID_0050348
obsolete primary Mycobacteriaceae infectious disease	DOID_0050347
obsolete opportunistic Nocardiaceae infectious disease	DOID_0050349
primary hyperoxaluria	DOID_2977	[A carbohydrate metabolic disorder characterized by impaired glyoxylate metabolism resulting in accumulation of oxalate throughout the body typically manifesting as kidney and bladder stones.]
obsolete commensal Pasteurellaceae infectious disease	DOID_0050371
obsolete commensal Neisseriaceae infectious disease	DOID_0050370
obsolete Leptospiraceae infectious disease	DOID_0050373
breast adenomyoepithelioma	DOID_1642	[A breast myoepithelial neoplasm that affects the breast and is characterized by biphasic proliferation of both epithelial and myoepithelial cells.]
obsolete commensal Haemophilus infectious disease	DOID_0050372
benign breast adenomyoepithelioma	DOID_1641	[A breast benign neoplasm that is characterized by dual differentiation into luminal cells and myoepithelial cells.]
obsolete primary Spirillaceae infectious disease	DOID_0050375
obsolete Spirochaetaceae infectious disease	DOID_0050374
obsolete Burkholderia cepacia complex infectious disease	DOID_0050377
obsolete anaplasmosis	DOID_0050376
autosomal recessive nonsyndromic deafness 76	DOID_0110524	[An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with high frequency, progressive hearing loss and has_material_basis_in mutation in the SYNE4 gene on chromosome 19q13.]
D_cluster	SO_0000559	[Genomic DNA of immunoglobulin/T-cell receptor gene in germline configuration including more than one D-gene.]
vertebrate_immunoglobulin_T_cell_receptor_gene_cluster	SO_0000482
autosomal recessive nonsyndromic deafness 77	DOID_0110525	[An autosomal recessive nonsyndromic deafness that is characterized by postlingual onset with moderate to profound, progressive hearing loss and has_material_basis_in mutation in the LOXHD1 gene on chromosome 18q21.]
C_cluster	SO_0000558	[Genomic DNA of immunoglobulin/T-cell receptor gene including more than one C-gene.]