Disease #04239 (hypometh. (hypomethylation))

Official abbreviation hypometh.
Name hypomethylation
OMIM ID -
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2015-04-06 21:46:14 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00037678 - PubMed: Lemmers 2015 SB_Fse(10%) F no France - - - - - hypometh. hypomethylation; digenic inheritance DUX4, SMCHD1 DUX4, SMCHD1 2 1 Richard Lemmers
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