Disease #05178 (MDST (dysplasia, metaphyseal, Spahr type (MDST)), OMIM:250400)
| Official abbreviation |
MDST |
| Name |
dysplasia, metaphyseal, Spahr type (MDST) |
| OMIM ID |
250400 |
| 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 |
MMP13 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2016-09-13 15:05:26 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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