Klippel-Feil Syndrome 2
Disease ID: disease_node_17382
Connections displayed (default: 10).
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| Dbxref | MIM:214300 |
|---|---|
| Subclassof | DOID_10426, DOID_0050737 |
| Data Source | DOID |
| Doid Label | Klippel-Feil syndrome 2 |
| Doid Description | A Klippel-Feil syndrome that has_material_basis_in homozygous mutation in the MEOX1 gene on chromosome 17q21. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_17382 |
| Doid Id | DOID_0080590 |
| Label | Klippel-Feil Syndrome 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Klippel-Feil Syndrome(ID:disease_node_4529) (Disease)