OBO ID: DOID:0080608
Term Name: anterior segment dysgenesis 3 Search Ontology:
Synonyms:
Definition: An anterior segment dysgenesis that has_material_basis_in heterozygous mutation in the FOXC1 gene on chromosome 6p25. https://www.ncbi.nlm.nih.gov/pubmed/27839872
References:
Ontology: Human Disease   (DOID:0080608)
OTHER anterior segment dysgenesis 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FOXC1 Anterior segment dysgenesis 3, multiple subtypes 601631
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None