Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
frontal lobe	UBERON_0016525
Pasteurellaceae	NCBITaxon_712
supported_by_EST_or_cDNA	SO_0000909	[An attribute to describe a feature that has been predicted using sequence similarity to EST or cDNA data.]
supported_by_sequence_similarity	SO_0000907	[An attribute to describe a feature that has been predicted using sequence similarity techniques.]
supported_by_domain_match	SO_0000908	[An attribute to describe a feature that has been predicted using sequence similarity of a known domain.]
independently_known	SO_0000906	[Attribute to describe a feature that is independently known - not predicted.]
rearranged_at_DNA_level	SO_0000904	[An attribute to describe the sequence of a feature, where the DNA is rearranged.]
epigenetically_modified	SO_0000133	[This attribute describes a gene where heritable changes other than those in the DNA sequence occur. These changes include: modification to the DNA (such as DNA methylation, the covalent modification of cytosine), and post-translational modification of histones.]
endogenous_retroviral_sequence	SO_0000903
transgene	SO_0000902	[A transgene is a gene that has been transferred naturally or by any of a number of genetic engineering techniques from one organism to another.]
labia minora carcinoma	DOID_1293	[A vulva carcinoma that is located_in the labia minora.]
autosomal dominant nonsyndromic deafness 58	DOID_0110582	[An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 2p21-p12.]
autosomal dominant nonsyndromic deafness 59	DOID_0110583	[An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 11p14.2-q12.3.]
obsolete thyroid gland tuberculosis	DOID_1269
autosomal dominant nonsyndromic deafness 54	DOID_0110580	[An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 5q31.]
autosomal dominant nonsyndromic deafness 56	DOID_0110581	[An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the TNC gene on chromosome 9q33.]
obsolete genitourinary cancer	DOID_1265	[An organ system cancer located_in the genitourinary system that is characterized by uncontrolled cellular proliferation in reproductive and urinary organs.]
Congenital agranulocytosis	HP_0005541	[Congenital onset of a marked decrease in the number of granulocytes.]
obsolete AIDS-related pelvic inflammatory disease	DOID_1261
autosomal dominant nonsyndromic deafness 67	DOID_0110588	[An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the OSBPL2 gene on chromosome 20q13.]