Disease #00194 (CWS1 (COWDEN SYNDROME 1), OMIM:158350)

Official abbreviation CWS1
Name COWDEN SYNDROME 1
OMIM ID 158350
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PTEN
Associated tissues -
Disease features -
Remarks -

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