Meckel Syndrome 8
Disease ID: disease_node_14685
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| Dbxref | ICD10CM:Q61.9, MIM:613885, ORDO:90674 |
|---|---|
| Subclassof | DOID_0050778 |
| Data Source | DOID |
| Synonyms | MKS8, Meckel-Gruber syndrome, type 8 |
| Doid Label | Meckel syndrome 8 |
| Doid Description | A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TCTN2 gene on chromosome 12q24.31. |
| Disease Node Id | disease_node_14685 |
| Doid Id | DOID_0070122 |
| Label | Meckel Syndrome 8 |
- Outgoing r'ship
SUBCLASS_OFto/from Meckel Syndrome(ID:disease_node_14683) (Disease)