Search Ontology:
Human Disease

anterior segment dysgenesis 8

Term ID
DOID:0080613
Synonyms
Definition
An anterior segment dysgenesis that has_material_basis_in homozygous or compound heterozygous mutation in the CPAMD8 gene on chromosome 19p13. https://www.ncbi.nlm.nih.gov/pubmed/27839872
References
Ontology
Human Disease   ( DOID:0080613 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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