Visceral Heterotaxy 7
Disease ID: disease_node_19904
Connections displayed (default: 10).
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| Dbxref | MIM:616749 |
|---|---|
| Subclassof | DOID_0050737, DOID_0050545 |
| Data Source | DOID |
| Doid Label | visceral heterotaxy 7 |
| Doid Description | A visceral heterotaxy that is characterized by complex congenital heart malformations and/or situs inversus and 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 MMP21 gene on chromosome 10q26. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19904 |
| Doid Id | DOID_0051021 |
| Label | Visceral Heterotaxy 7 |
- 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)