Disease #05359 (MEAX (myopathy, X-linked, with excessive autophagy (MEAX)), OMIM:310440)
Official abbreviation |
MEAX |
Name |
myopathy, X-linked, with excessive autophagy (MEAX) |
OMIM ID |
310440 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked recessive |
Individuals reported having this disease |
19 |
Phenotype entries for this disease |
19 |
Associated with 1 gene |
VMA21 |
Associated tissues |
- |
Disease features |
X-linked recessive |
Remarks |
- |
Date created |
2017-12-28 17:22:37 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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