Search Ontology:
Human Disease

optic disc anomalies with retinal and/or macular dystrophy

Term ID
DOID:0080635
Synonyms
Definition
A microphthalmia that has_material_basis_in homozygous mutation in the SIX6 gene on chromosome 14q23. https://www.ncbi.nlm.nih.gov/pubmed/24702266
References
Ontology
Human Disease   ( DOID:0080635 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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