Disease #04441 (SGMRT2 (Singleton-Merten syndrome, type 2 (SGMRT-2)), OMIM:616298)

Official abbreviation SGMRT2
Name Singleton-Merten syndrome, type 2 (SGMRT-2)
OMIM ID 616298
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene DDX58
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00306232 140 - - F - China - - - - - SGMRT2 - DDX58 DDX58 1 1 Sha Hong
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