Annotation Detail

Information
Associated Genes
VHL
Associated Variants
VHL MUTATION
VHL MUTATION
Associated Disease
pheochromocytoma
Source Database
DisGeNET
Description
VHL gene mutation analysis of a Chinese family with non- syndromic pheochromocytomas and patients with apparently sporadic pheochromocytoma.
Pubmed
25773797
Section of the abstract supporting the evidence
TITLE
Number of the section of the abstract supporting the evidence
0
Number of the sentence supporting the evidence
0
Original source reporting the Gene Disease association
BeFree,CLINVAR,CTD_human,GAD,LHGDN,UNIPROT
DisGENET score for the Gene Disease association
0.415849807388327
Drugs