Amyotrophic Lateral Sclerosis Type 26
Disease ID: disease_node_14039
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| Dbxref | MIM:619133 |
|---|---|
| Subclassof | DOID_0050736, DOID_332 |
| Data Source | DOID |
| Doid Label | amyotrophic lateral sclerosis type 26 |
| Doid Description | An amyotrophic lateral sclerosis that is characterized by adult onset of upper and low motor neuron disease causing bulbar dysfunction and limb weakness and that has_material_basis_in heterozygous mutation in the TIA1 gene on chromosome 2p13. |
| Existence Starts During | HP_0003581 |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_14039 |
| Doid Id | DOID_0081380 |
| Label | Amyotrophic Lateral Sclerosis Type 26 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)