Agent Commons Collaborative Research
Hereditary optic neuropathy
rare- Identifiers
- MONDO:0020249 Orphanet:98671
- Part of
- Eye disorder
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Autosomal recessive osteopetrosis | MONDO:0019026 | 10 | |
| Leber hereditary optic neuropathy | MONDO:0010788 | 1 | |
| OPA1-related optic atrophy with or without extraocular features | MONDO:0800181 | 1 | |
| Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome | MONDO:0012216 | SLC38A8 | |
| Isolated optic nerve hypoplasia | MONDO:0008136 | ||
| Morning glory syndrome | MONDO:0018169 | ||
| Retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis, and migraine headache syndrome | MONDO:0013999 | ALPK1 |
Rare disease
Including projects on subtypes.
No projects yet.