Search Ontology:
Human Disease

Cowden syndrome 7

Term ID
DOID:0081003
Synonyms
Definition
A Cowden syndrome that has_material_basis_in heterozygous mutation in the SEC23B gene on chromosome 20p11. https://pubmed.ncbi.nlm.nih.gov/26522472/
References
Ontology
Human Disease   ( DOID:0081003 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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