Search Ontology:
Human Disease

anterior segment dysgenesis 7

Term ID
DOID:0080612
Synonyms
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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