All terms in DOID

Label Id Description
X-linked endothelial corneal dystrophy DOID_0060446 [A corneal endothelial dystrophy that is characterized by congenital ground glass corneal clouding or a diffuse corneal haze, and blurred vision in male patients.]
epithelial basement membrane dystrophy DOID_0060447 [An epithelial and subepithelial dystrophy that is characterized by sheet-like areas of basement membrane originating from the basal epithelial cells of the corneal epithelium and extending superficially into the epithelium.]
Fleck corneal dystrophy DOID_0060448 [A stromal dystrophy that is characterized by numerous tiny, dot-like white flecks scattered in all layers of the corneal stroma and that has_material_basis_in heterozygous mutation in the PIKFYVE gene on chromosome 2q34.]
gelatinous drop-like corneal dystrophy DOID_0060449 [An epithelial and subepithelial dystrophy that is characterized by severe corneal amyloidosis leading to blindness and that has_material_basis_in homozygous or compound heterozygous mutation in the TACSTD2 gene which encodes the monoclonal antibody-defined, tumor-associated antigen GA733-1, on chromosome 1p32.]
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
oculomotor nerve UBERON_0001643
trochlear nerve UBERON_0001644
breast UBERON_0000310
external soft tissue zone UBERON_0034929
vein UBERON_0001638
venous blood vessel UBERON_0003920
tendon sheath UBERON_0000304
arterial blood vessel UBERON_0003509