congenital bilateral absence of vas deferens
Information
- Disease name
- congenital bilateral absence of vas deferens
- Disease ID
- DOID:0111862
- Description
- "A male infertility that is characterized by bilateral absence of the vas deferens resulting in obstroctive azoospermia and male infertility." [url:https\://pubmed.ncbi.nlm.nih.gov/27476656/]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT06045702 | Not yet recruiting | Establishment of a Primary Epididymal Cell Model From Epididymal Samples to Study CFTR Gene Regulation | September 2023 | September 2025 |
- Disase is a (Disease Ontology)
- DOID:12336
- Cross Reference ID (Disease Ontology)
- MIM:PS277180
- Cross Reference ID (Disease Ontology)
- ORDO:48
- Exact Synonym (Disease Ontology)
- CAVD
- Exact Synonym (Disease Ontology)
- CBAVD
- Exact Synonym (Disease Ontology)
- congenital bilateral agenesis of vas deferens
- Exact Synonym (Disease Ontology)
- congenital bilateral aplasia of vas deferens
- OrphaNumber from OrphaNet (Orphanet)
- 48