Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9150
Gene Symbol: CTDP1
CTDP1
CUI: C0086543
Disease: Cataract
Cataract 		0.110 GeneticVariation LHGDN Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome. 14517542

2003