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
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