Disease #00050 (TPDS (TUMOR PREDISPOSITION SYNDROME), OMIM:614327)

Official abbreviation TPDS
Name TUMOR PREDISPOSITION SYNDROME
OMIM ID 614327
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene BAP1
Associated tissues -
Disease features -
Remarks -
Date created 2020-03-03 14:26:28 +00:00 (UTC)
Date last edited N/A