idiopathic macular telangiectasia type 3
http://purl.obolibrary.org/obo/MONDO_0018147
A rare, acquired, eye disease characterized by progressive visual loss, due to bilateral juxtafoveolar capillary occlusions, capillary telangiectasia, and minimal exudation. It is associated with systemic or cerebral vascular occlusive disease. [ Orphanet:353351 https://orcid.org/0000-0001-5208-3432 ]
Term info
- Orphanet:353351 (MONDO:equivalentTo)
- UMLS:CN204545 (MONDO:equivalentTo)
- ICD10CM:H35.5 (Orphanet:353351/ntbt)
ordo_disease
A rare, acquired, eye disease characterized by progressive visual loss, due to bilateral juxtafoveolar capillary occlusions, capillary telangiectasia, and minimal exudation. It is associated with systemic or cerebral vascular occlusive disease.
http://purl.obolibrary.org/obo/Orphanet_353351, http://linkedlifedata.com/resource/umls/id/CN204545
occlusive idiopathic juxtafoveolar retinal telangiectasis
MONDO:0018147