About   Help   FAQ
Disease Ontology Browser
congenital muscular dystrophy 1B (DOID:0110634)
Synonyms: CMD1B; congenital muscular dystrophy type 1B; MDC1B
Alt IDs: OMIM:604801, ICD10CM:G71.2, ORDO:98893
Definition: A congenital muscular dystrophy characterized by autosomal recessive inheritance of proximal muscle weakness, muscle hypertrophy, and early respiratory failure that has_material_basis_in variation in the chromosome region 1q42.


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
04/18/2017
MGI 6.08
The Jackson Laboratory