Search Ontology:
Human Disease

pancreatic agenesis 1

Term ID
DOID:0061003
Synonyms
Definition
A pancreatic agenesis characterized by intrauterine growth retardation that has_material_basis_in homozygous or compound heterozygous mutation in the PDX1 gene on chromosome 13q12. https://pubmed.ncbi.nlm.nih.gov/20009086/
References
Ontology
Human Disease   ( DOID:0061003 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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