OBO ID: DOID:0080840
Term Name: optic atrophy 12 Search Ontology:
Synonyms:
Definition: An optic atrophy that is characterized by slowly progressive visual impairment with onset usually in the first decade and that has_material_basis_in heterozygous mutation in the AFG3L2 gene on chromosome 18p11. https://pubmed.ncbi.nlm.nih.gov/32219868/
References:
Ontology: Human Disease   ( DOID:0080840 )
Relationships
is a type of:
OTHER optic atrophy 12 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
AFG3L2 Optic atrophy 12 618977
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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