Autosomal Recessive Congenital Bilateral Absence Of Vas Deferens
Disease ID: disease_node_17152
Connections displayed (default: 10).
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| Dbxref | MIM:277180 |
|---|---|
| Subclassof | DOID_0111862, DOID_0050737 |
| Data Source | DOID |
| Doid Label | autosomal recessive congenital bilateral absence of vas deferens |
| Doid Description | A congenital bilateral absence of vas deferens that has_material_basis_in homozygous or compound heterozygous mutation in the CFTR gene on chromosome 7q31.2. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_17152 |
| Doid Id | DOID_0111864 |
| Disease Has Basis In | HP_0001197 |
| Label | Autosomal Recessive Congenital Bilateral Absence Of Vas Deferens |
- Outgoing r'ship
SUBCLASS_OFto/from Congenital Bilateral Absence Of Vas Deferens(ID:disease_node_17151) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)