OBO ID: DOID:0081003
Term Name: Cowden syndrome 7 Search Ontology:
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 Cowden syndrome 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SEC23B ?Cowden syndrome 7 616858
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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