congenital myasthenic syndrome 6

Summary

DOID:0110671 - congenital myasthenic syndrome 6

Disease Ontology Definition:A congenital myasthenic syndrome characterized by autosomal recessive inheritance of a presynaptic defect resulting in onset of muscle weakeness in infancy or early childhood and a tendency to have sudden apneic episodes that has_material_basis_in homozygous or compound heterozygous mutation in the CHAT gene on chromosome 10q.

Synonyms: CMS1A2, CMS6, CMSEA, CMS Ia2, congenital myasthenic syndrome 6, presynaptic, congenital myasthenic syndrome type Ia2, congenital presynaptic myasthenic syndrome associated with episodic apnea, familial infantile myasthenia, familial infantile myasthenia gravis 2, FIM, FIMG2

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: chat

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009689 - congenital myasthenic syndrome 6

MONDO:0009689 - congenital myasthenic syndrome 6

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), congenital myasthenic syndrome (is_a)