Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
obsolete glomerular vascular disorder	DOID_2976
antiphospholipid syndrome	DOID_2988	[An autoimmune hypersensitivity disease that is characterized by recurrent venous or arterial thrombosis and/or fetal losses associated with characteristic elevated levels of antibodies directed against membrane anionic phospholipids (anticardiolipin).]
Arterial thrombosis	HP_0004420	[The formation of a blood clot inside an artery.]
obsolete commensal Enterobacteriaceae infectious disease	DOID_0050360
obsolete Atypical small acinar proliferation of the prostate gland	DOID_2989
obsolete Elizabethkingia meningoseptica infectious disease	DOID_0050362
obsolete opportunistic Enterobacteriaceae infectious disease	DOID_0050361
obsolete opportunistic Flavobacteriaceae infectious disease	DOID_0050364
obsolete Capnocytophaga canimorsus infectious disease	DOID_0050363
female breast axillary tail cancer	DOID_1650	[A female breast cancer that is located_in the breast tissue extending into the axilla.]
obsolete Empedobacter brevis endophthalmitis	DOID_0050366
obsolete Chryseobacterium indologenes infectious disease	DOID_0050365
inversion_derived_duplication_plus_aneuploid	SO_0000549	[A chromosome generated by recombination between two inversions; has a duplication at one end and presumed to have a deficiency or duplication at the other end of the inversion.]
autosomal recessive nonsyndromic deafness 61	DOID_0110513	[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 SLC26A5 gene on chromosome 7q22.]
gene_with_edited_transcript	SO_0000548	[A gene that encodes a transcript that is edited.]
autosomal recessive nonsyndromic deafness 62	DOID_0110514	[An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 12p13.2-p11.23.]
inversion_derived_bipartite_duplication	SO_0000547	[A chromosome generated by recombination between two inversions; there is a duplication at each end of the inversion.]
autosomal recessive nonsyndromic deafness 59	DOID_0110511	[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 DFNB59 gene on chromosome 2q31.]
designed_sequence	SO_0000546
synthetic_sequence	SO_0000351	[An attribute to decide a sequence of nucleotides, nucleotide analogs, or amino acids that has been designed by an experimenter and which may, or may not, correspond with any natural sequence.]