OBO ID: DOID:0111440 |
Term Name: | optic atrophy 4 | Search Ontology: | |
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Synonyms: |
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Definition: | An optic atrophy that has_material_basis_in heterozygous mutation in a region on chromosome 18q12.2-q12.3. https://www.ncbi.nlm.nih.gov/pubmed/10369594 | ||
References: | |||
Ontology: | Human Disease ( DOID:0111440 ) |
OTHER optic atrophy 4 PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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