Disease #04261 (SEDT (dysplasia, spondyloepiphyseal, tarda (SEDT)))
Official abbreviation |
SEDT |
Name |
dysplasia, spondyloepiphyseal, tarda (SEDT) |
OMIM ID |
- |
Inheritance |
- |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
COL2A1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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