Disease #02180 (RBMX1A (myopathy, reducing body, X-linked, type 1a (RBMX-1A)), OMIM:300717)
| Official abbreviation |
RBMX1A |
| Name |
myopathy, reducing body, X-linked, type 1a (RBMX-1A) |
| OMIM ID |
300717 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
FHL1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
X-linked dominant, severe, infantile or early childhood onset |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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