Visceral Heterotaxy 8
Disease ID: disease_node_19903
Connections displayed (default: 10).
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| Dbxref | MIM:617205 |
|---|---|
| Subclassof | DOID_0050737, DOID_0050545 |
| Data Source | DOID |
| Doid Label | visceral heterotaxy 8 |
| Doid Description | A visceral heterotaxy that is characterized by visceral situs inversus associated with complex congenital heart malformations caused by defects in the normal left-right asymmetric positioning of internal organs and that has_material_basis_in homozygous or compound heterozygous mutation in the PKD1L1 gene on chromosome 7p12. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19903 |
| Doid Id | DOID_0051022 |
| Label | Visceral Heterotaxy 8 |
- Outgoing r'ship
SUBCLASS_OFto/from Visceral Heterotaxy(ID:disease_node_19897) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)