Disease #05453 (SMABF2 (atrophy, muscular, spinal, with congenital bone fractures, type 2 (SMABF2)), OMIM:616867)
| Official abbreviation |
SMABF2 |
| Name |
atrophy, muscular, spinal, with congenital bone fractures, type 2 (SMABF2) |
| OMIM ID |
616867 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ASCC1 |
| Associated tissues |
- |
| Disease features |
autosomal recessive |
| Remarks |
- |
| Date created |
2018-07-09 15:52:08 +02:00 (CEST) |
| Date last edited |
2020-03-03 16:18:21 +01:00 (CET) |
Individuals
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