Disease #04195 (SGMRT1 (Singleton-Merten syndrome, type 1 (SGMRT-1)), OMIM:182250)

Official abbreviation SGMRT1
Name Singleton-Merten syndrome, type 1 (SGMRT-1)
OMIM ID 182250
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene IFIH1
Associated tissues -
Disease features -
Remarks -
Date created 2015-02-15 21:43:59 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00032346 - PubMed: Rutsch 2015, Journal: Rutsch 2015 5-generation family, 17 affecteds (8F, 9M) - - - - - - - - SGMRT1 see paper; .. IFIH1 IFIH1 1 17 Johan den Dunnen
00032347 - PubMed: Rutsch 2015, Journal: Rutsch 2015 2-generation family, 3 affecteds (1F, 2M) - no - - - - - - SGMRT1 see paper; .. IFIH1 IFIH1 1 3 Johan den Dunnen
00032348 - PubMed: Rutsch 2015, Journal: Rutsch 2015 2-generation family, 1 affected F no - - - - - - SGMRT1 see paper; .. IFIH1, SPECC1L IFIH1, SPECC1L 2 1 Johan den Dunnen
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