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

1 entry on 1 page. Showing entry 1.
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00306232 140 - - F - China - - - - - SGMRT-2 - DDX58 DDX58 1 1 Sha Hong
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