Search Ontology:
Human Disease
anterior segment dysgenesis 7
- Term ID
- DOID:0080612
- Synonyms
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- Definition
- An anterior segment dysgenesis that has_material_basis_in homozygous or compound heterozygous mutation in the PXDN gene on chromosome 2p25. https://www.ncbi.nlm.nih.gov/pubmed/27839872
- References
- Ontology
- Human Disease ( DOID:0080612 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models