Visceral Heterotaxy 10
Disease ID: disease_node_19901
Connections displayed (default: 10).
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| Dbxref | MIM:619607 |
|---|---|
| Subclassof | DOID_0050737, DOID_0050545 |
| Data Source | DOID |
| Doid Label | visceral heterotaxy 10 |
| Doid Description | A visceral heterotaxy that is characterized by a failure to generate normal left-right visceral asymmetry during embryogenesis, which can result in heterotaxy syndrome or situs inversus totalis and that has_material_basis_in homozygous mutation in the CFAP52 gene on chromosome 17p13. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19901 |
| Doid Id | DOID_0051024 |
| Label | Visceral Heterotaxy 10 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Visceral Heterotaxy(ID:disease_node_19897) (Disease)