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

Official abbreviation CWS-2
Name Cowden syndrome, type 2 (CWS-2)
OMIM ID 612359
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SDHB
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A