Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
Aureobasidium	NCBITaxon_5579
Saccotheciaceae	NCBITaxon_1570301
Reis-Bucklers corneal dystrophy	DOID_0060453	[An epithelial-stromal TGFBI dystrophy that is characterized by recurrent erosions and irregular geographic opacification located_in the cornea, proteinaceous deposits in the anterior stroma and subepithelium, and progressive early vision loss, and has_material_basis in heterozygous mutation of transforming growth factor beta-induced gene located in chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased protein deposition and disruption especially of Bowman's membrane of the cornea.]
apocrine sweat gland	UBERON_0000382
corneal dystrophy	DOID_2566
granular corneal dystrophy 2	DOID_0060444	[An corneal granular dystrophy that is characterized by recurrent erosions and stellate or thorn-like opacification located_in the cornea, hyaline and amyloid deposits in the stroma, and progressive vision loss later in life, and has_material_basis_in autosomal dominant inheritance of mutation of transforming growth factor beta-induced gene on chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased hyaline and amyloid protein deposition and disruption of the corneal surface.]
granular corneal dystrophy	DOID_12318	[An epithelial-stromal TGFBI dystrophy that is characterized by progressive accumulation of deposits within the layers of the cornea.]
congenital stromal corneal dystrophy	DOID_0060445
X-linked endothelial corneal dystrophy	DOID_0060446
epithelial basement membrane dystrophy	DOID_0060447
Fleck corneal dystrophy	DOID_0060448
gelatinous drop-like corneal dystrophy	DOID_0060449
epiglottis	UBERON_0000388
foramen of skull	UBERON_0013685
bone foramen	UBERON_0005744
digitopodium bone	UBERON_0012357
autopod bone	UBERON_0011250
vasculature of central nervous system plus retina	UBERON_0036302
vasculature	UBERON_0002049
vasculature of central nervous system	UBERON_0036303