Disease #01963 (NEM2 (myopathy, nemaline, type 2 (NEM2)), OMIM:256030)
| Official abbreviation |
NEM2 |
| Name |
myopathy, nemaline, type 2 (NEM2) |
| OMIM ID |
256030 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
11 |
| Phenotype entries for this disease |
11 |
| Associated with 1 gene |
NEB |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-09-30 10:59:30 +02:00 (CEST) |
Individuals
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