Disease #03129 (CWS2 (Cowden syndrome, type 2 (CWS-2)), OMIM:612359)

Official abbreviation CWS2
Name Cowden syndrome, type 2 (CWS-2)
OMIM ID 612359
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SDHB
Associated tissues -
Disease features -
Remarks -