Disease #04562 (NEM10 (myopathy, nemaline, type 10 (NEM-10)), OMIM:616165)
Official abbreviation |
NEM10 |
Name |
myopathy, nemaline, type 10 (NEM-10) |
OMIM ID |
616165 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
LMOD3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|