Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 116372
Gene Symbol: LYPD1
LYPD1
CUI: C0271829
Disease: Pendred's syndrome
Pendred's syndrome 		0.010 GeneticVariation BEFREE The first group includes familial syndromes characterized by a predominance of non-thyroidal tumors, such as familial adenomatous polyposis (FAP), PTEN-hamartoma tumor syndrome (Cowden disease; PHTS), Carney complex, Werner syndrome, and Pendred syndrome. 20878367

2010