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hereditary optic atrophy

Disease Summary
Associated Targets (27)
Tbio

13

Tclin

10

Tchem

4


Mondo Description A family of inherited disorders characterized by progressive loss of vision secondary to death of the retinal ganglion cell axons that comprise the optic nerve.
Mondo Term and Equivalent IDs
MONDO:0043878:  hereditary optic atrophy
MESH:D015418: 
NCIT:C34864: 
OMIMPS:165500: 
SCTID:26360005: 
UMLS:C0029125: