Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 27031
Gene Symbol: NPHP3
NPHP3
CUI: C0016059
Disease: Fibrosis
Fibrosis 		0.010 GeneticVariation LHGDN We describe mutations in NPHP3 in families with isolated NPHP and in families with NPHP with associated hepatic fibrosis or tapeto-retinal degeneration. 12872122

2003