Search Ontology:
Human Disease
anterior segment dysgenesis 2
- Term ID
- DOID:0080607
- 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 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models
Citations