Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Nervous system disorder
/
Hereditary neurological disease
/
Inherited neurodegenerative disorder
/
Hereditary optic atrophy
Optic atrophy 12
rare
Identifiers
MONDO:0033549
OMIM:618977
Part of
AFG3L2-related optic atrophy and/or spastic ataxia spectrum
Hereditary optic atrophy
Also known as
OPA12
Projects
Sign in to start a project
No projects yet.