Meier-Gorlin Syndrome 5
Disease ID: disease_node_20119
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| Dbxref | MIM:613805 |
|---|---|
| Subclassof | DOID_0060306, DOID_0050737 |
| Data Source | DOID |
| Doid Label | Meier-Gorlin syndrome 5 |
| Doid Description | A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDC6 gene on chromosome 17q21. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_20119 |
| Doid Id | DOID_0080516 |
| Label | Meier-Gorlin Syndrome 5 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)