Meckel Syndrome 5
Disease ID: disease_node_14687
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| Dbxref | ICD10CM:Q61.9, MIM:611561 |
|---|---|
| Subclassof | DOID_0050778 |
| Data Source | DOID |
| Synonyms | MKS5, Meckel-Gruber syndrome, type 5 |
| Doid Label | Meckel syndrome 5 |
| Doid Description | A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the RPGRIP1L gene on chromosome 16q12.2. |
| Disease Node Id | disease_node_14687 |
| Doid Id | DOID_0070119 |
| Label | Meckel Syndrome 5 |
- Outgoing r'ship
SUBCLASS_OFto/from Meckel Syndrome(ID:disease_node_14683) (Disease)