Congenital Myasthenic Syndrome 15
Disease ID: disease_node_14300
Connections displayed (default: 10).
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| Dbxref | MIM:616227 |
|---|---|
| Subclassof | DOID_0050737, DOID_3635 |
| Data Source | DOID |
| Synonyms | CMS15, congenital myasthenic syndrome 15 without tubular aggregates |
| Doid Label | congenital myasthenic syndrome 15 |
| Doid Description | A congenital myasthenic syndrome characterized by onset of progressive fatigable proximal muscle weakness in childhood that has_material_basis_in compound heterozygous mutation in the ALG14 gene on chromosome 1p21. |
| Has Symptom | SYMP_0000094 |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_14300 |
| Doid Id | DOID_0110658 |
| Disease Has Basis In | HP_0001197 |
| Label | Congenital Myasthenic Syndrome 15 |
- Outgoing r'ship
HAS_SYMPTOMto/from Muscle Weakness(ID:disease_node_9835;disease_node_21022) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Myasthenic Syndromes, Congenital(ID:disease_node_10478) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)