fundus dystrophy

Summary

fundus dystrophy is a class of disease^[1].

Key Facts

• fundus dystrophy's instance of is recorded as class of disease^[2].
• fundus dystrophy's subclass of is recorded as eye disease^[3].
• fundus dystrophy's subclass of is recorded as retinal degeneration^[4].
• fundus dystrophy's subclass of is recorded as genetic vitreous-retinal disease^[5].
• fundus dystrophy's MeSH descriptor ID is recorded as D058499^[6].
• fundus dystrophy's DiseasesDB is recorded as 9580^[7].
• fundus dystrophy's MeSH tree code is recorded as C11.768.585.658^[8].
• fundus dystrophy's Disease Ontology ID is recorded as DOID:8501^[9].
• fundus dystrophy's Orphanet ID is recorded as 71862^[10].
• fundus dystrophy's ICD-9-CM is recorded as 362.75^[11].
• fundus dystrophy's ICD-9-CM is recorded as 362.72^[12].
• fundus dystrophy's NCI Thesaurus ID is recorded as C35625^[13].
• fundus dystrophy's health specialty is recorded as ophthalmology^[14].
• fundus dystrophy's genetic association is recorded as RLBP1^[15].
• fundus dystrophy's genetic association is recorded as RDH5^[16].
• fundus dystrophy's genetic association is recorded as LCA5^[17].
• fundus dystrophy's genetic association is recorded as RPE65^[18].
• fundus dystrophy's genetic association is recorded as OTX2^[19].
• fundus dystrophy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_8501^[20].
• fundus dystrophy's exact match is recorded as http://identifiers.org/doid/DOID:8501^[21].
• fundus dystrophy's exact match is recorded as http://purl.obolibrary.org/obo/HP_0000556^[22].
• fundus dystrophy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_71862^[23].
• fundus dystrophy's UMLS CUI is recorded as C0854723^[24].
• fundus dystrophy's Human Phenotype Ontology ID is recorded as HP:0000556^[25].
• fundus dystrophy's on focus list of Wikimedia project is recorded as WikiProject Medicine^[26].