reticular dystrophy of the retinal pigment epithelium
Go to external page http://purl.obolibrary.org/obo/MONDO_0009979
Reticular dystrophy of the retinal pigment epithelium is a patterned dystrophy of the retinal pigment epithelium, of progressive course, characterized by the presence of a bilateral hyperpigmented reticular pattern resembling a fishnet with knots, resulting in a slowly progressive loss of vision that often only becomes apparent in old age. Reticular dystrophy of the retinal pigment epithelium is sometimes associated with scleral staphyloma, choroidal neovascularization, convergent strabismus, spherophakia with myopia and luxated lenses, and partial atrophy of the iris. [ Orphanet:99002 ]
Synonyms: reticular dystrophy of retinal pigment epithelium
Term information
- MESH:C566721 (MONDO:equivalentTo)
- Orphanet:99002 (OMIM:267800)
- SCTID:723502001 (MONDO:equivalentTo)
- GARD:16891 (Orphanet:99002)
- MESH:C564844 (MONDO:mondoIsBroaderThanSource)
- GARD:18239 (OMIM:179840)
- ICD10CM:H35.5 (Orphanet:99002/ntbt)
- OMIM:267800 (Orphanet:99002/e)
- OMIM:179840 (Orphanet:99002/btnt)
- UMLS:C1849407 (OMIM:267800)
gard_rare, ordo_disease, rare, nord_rare, orphanet_rare
http://identifiers.org/snomedct/723502001
http://linkedlifedata.com/resource/umls/id/C1849407
https://omim.org/entry/179840
http://identifiers.org/mesh/C566721
http://www.orpha.net/ORDO/Orphanet_99002