OBO ID: DOID:0080612
Term Name: anterior segment dysgenesis 7 Search Ontology:
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 anterior segment dysgenesis 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PXDN Anterior segment dysgenesis 7, with sclerocornea 269400
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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