Annotation Detail
Information
- Associated Genes
- CFTR
- Associated Variants
-
CFTR MUTATION
CFTR MUTATION - Associated Disease
- Congenital bilateral aplasia of vas deferens
- Source Database
- DisGeNET
- Description
- Novel mutations and polymorphisms in the CFTR gene associated with three subtypes of congenital absence of vas deferens.
- Pubmed
- 26277102
- 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,ORPHANET,UNIPROT
- DisGENET score for the Gene Disease association
- 0.509163832444431
Drugs