WormBase Tree Display for DO_term: DOID:0110663
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DOID:0110663 | Name | congenital myasthenic syndrome 1A | |||
---|---|---|---|---|---|
Status | Valid | ||||
Definition | A congenital myasthenic syndrome characterized by predominantly autosomal dominant inheritance of defects in postsynaptic neuromuscular junctions and early-onset progressive muscle weakness that has_material_basis_in mutation in the CHRNA1 gene on chromosome 2q. | ||||
Synonym | Exact (4) | ||||
Parent | Is_a | DOID:3635 | |||
DOID:0050736 | |||||
DB_info | Database | OMIM | disease | 601462 | |
Attribute_of | Gene_by_orthology | WBGene00000043 | |||
WBGene00000047 | |||||
WBGene00000051 | |||||
WBGene00002974 | |||||
WBGene00002975 | |||||
WBGene00006765 | |||||
WBGene00006774 | |||||
WBGene00006797 |