Disease #00363 (MYPBB (myopathy, congenital, Baily-Bloch), OMIM:255995)
Official abbreviation |
MYPBB |
Name |
myopathy, congenital, Baily-Bloch |
OMIM ID |
255995 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
STAC3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-03-27 19:33:47 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|