Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
parametritis	DOID_1260
autosomal dominant nonsyndromic deafness 68	DOID_0110589	[An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the HOMER2 gene on chromosome 15q25.]
autosomal dominant nonsyndromic deafness 65	DOID_0110586	[An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the TBC1D24 gene on chromosome 16p13.]
autosomal dominant nonsyndromic deafness 66	DOID_0110587	[An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CD164 gene on chromosome 6q21.]
autosomal dominant nonsyndromic deafness 6	DOID_0110584	[An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and low frequency progressive hearing loss and has_material_basis_in mutation in the WFS1 gene on chromosome 4p16.]
autosomal dominant nonsyndromic deafness 64	DOID_0110585	[An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the DIABLO gene on chromosome 12q24.]
Haemophilus	NCBITaxon_724
obsolete nephrotic syndrome with lesion of lobular glomerulonephritis	DOID_2591
obsolete nephrotic syndrome with lesion of focal glomerulosclerosis	DOID_2592
glottis cancer	DOID_2595
glottis neoplasm	DOID_2597
Actinobacillus	NCBITaxon_713
glottis	UBERON_0002486
autosomal dominant nonsyndromic deafness 48	DOID_0110571	[An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with progressive hearing loss and has_material_basis_in variation in the chromosome region 12q13-q14.]
autosomal dominant nonsyndromic deafness 49	DOID_0110572	[An autosomal dominant nonsyndromic deafness that is characterized by moderate loss for low and mid frequencies and mild loss for high frequencies and has_material_basis_in variation in the chromosome region 1q21-q23.]
autosomal dominant nonsyndromic deafness 47	DOID_0110570	[An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 9p22-p21.]
tolosa-hunt syndrome	DOID_1278
single fate stem cell	CL_0000035
obsolete Pneumovirus infectious disease	DOID_1275	[A Paramyxoviridae infectious disease that results_in infection in cattle and humans, has_material_basis_in Pneumovirus, which is transmitted_by contact with the respiratory secretions.]
autosomal dominant nonsyndromic deafness 53	DOID_0110579	[An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 14q11.2-q12.]