Disease #05499 (OPA5 (atrophy, optic, type 5 (OPA-5)), OMIM:610708)

Official abbreviation OPA5
Name atrophy, optic, type 5 (OPA-5)
OMIM ID 610708
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene DNM1L
Associated tissues -
Disease features autosomal dominant
Remarks -

  Powered by LOVD v.3.0 Build 27
LOVD software ©2004-2022 Leiden University Medical Center 		There are currently no updates.