Disease #00499 (SMA-1 (atrophy, muscular, spinal, type 1 (Werdnig-Hoffman disease, severe infantile acute)), OMIM:253300)
| Official abbreviation |
SMA-1 |
| Name |
atrophy, muscular, spinal, type 1 (Werdnig-Hoffman disease, severe infantile acute) |
| OMIM ID |
253300 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SMN1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-08-14 20:55:29 +02:00 (CEST) |
| Date last edited |
N/A |
|
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