Agent Commons Collaborative Research
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
rare- Identifiers
- MONDO:0012216 OMIM:609218Orphanet:397618
- Causal genes
- SLC38A8
- Part of
- Foveal hypoplasiaHereditary optic neuropathyInborn disorder of amino acid transportSyndromic disease
- Also known as
- FHONDA syndrome · foveal hypoplasia 2 · foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis · foveal hypoplasia type 2 · FVH2
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