OBO ID: DOID:0080607
Term Name: anterior segment dysgenesis 2 Search Ontology:
Synonyms:
Definition: An anterior segment dysgenesis that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the FOXE3 gene on chromosome 1p33. https://www.ncbi.nlm.nih.gov/pubmed/21150893
References:
Ontology: Human Disease   ( DOID:0080607 )
Relationships
is a type of:
OTHER anterior segment dysgenesis 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FOXE3 Anterior segment dysgenesis 2, multiple subtypes 610256
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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