Disease #02971 (NEM7 (myopathy, nemaline, type 7 (NEM-7)), OMIM:610687)
Official abbreviation |
NEM7 |
Name |
myopathy, nemaline, type 7 (NEM-7) |
OMIM ID |
610687 |
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 |
CFL2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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