Disease #04441 (SGMRT-2 (Singleton-Merten syndrome, type 2 (SGMRT-2)), OMIM:616298)
Official abbreviation |
SGMRT-2 |
Name |
Singleton-Merten syndrome, type 2 (SGMRT-2) |
OMIM ID |
616298 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
DDX58 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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