WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0060453 Reis-Bucklers corneal dystrophy Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  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.

1 Ontology

Name
Disease Ontology

9 Parents

Identifier Name Description
DOID:7 disease of anatomical entity A disease that manifests in a defined anatomical structure.
DOID:4 disease A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:10124 corneal disease An eye disease that affects the cornea, which is the transparent surface of the eye that assists in light refraction.
DOID:863 nervous system disease A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system.
DOID:5614 eye disease An eye and adnexa disease that is located_in the eye.
DOID:0050155 sensory system disease A nervous system disease which is located in a part of the nervous system responsible for processing sensory information that consists of sensory receptors, neural pathways, and parts of the brain involved in sensory perception. Commonly recognized sensory systems are those for vision, hearing, somatic sensation (touch), taste and olfaction (smell).
DOID:2566 corneal dystrophy  
DOID:0060441 epithelial-stromal TGFBI dystrophy A corneal dystrophy that is characterized by abnormal deposition of proteins in the cornea and is caused by mutations in TGFBI gene of chromosome 5q.
DOID:0060453 Reis-Bucklers corneal dystrophy 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.

8 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0060441 DOID:0060453
is_a DOID:7 DOID:0060453
is_a DOID:4 DOID:0060453
is_a DOID:10124 DOID:0060453
is_a DOID:5614 DOID:0060453
is_a DOID:0050155 DOID:0060453
is_a DOID:863 DOID:0060453
is_a DOID:2566 DOID:0060453

5 Synonyms

Name Type
anterior limiting membrane dystrophy type I synonym
corneal dystrophy of Bowman layer type I synonym
geographic corneal dystrophy synonym
granular corneal dystrophy type III synonym
RBCD synonym