Disease #00502 (SMA4 (atrophy, muscular, spinal, type IV (SMA-4, adult)), OMIM:271150)
Official abbreviation |
SMA4 |
Name |
atrophy, muscular, spinal, type IV (SMA-4, adult) |
OMIM ID |
271150 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
SMN1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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