About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease

Term: Myasthenic Syndrome, Congenital, Associated with Episodic Apnea
OMIM ID: 254210

Synonyms CMS-EA; Cms Ia2; Congenital Myasthenic Syndrome Type Ia2; CMS1A2; Myasthenia, Familial Infantile; FIM; Myasthenia Gravis, Familial Infantile, 2, Formerly; FIMG2, FORMERLY; Myasthenic Syndrome, Presynaptic, Congenital, Associated with Episodic Apnea
Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
     
Chat CHAT
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory