Disease #05102 (STROMS (Stromme syndrome (STROMS)), OMIM:243605)

Official abbreviation STROMS
Name Stromme syndrome (STROMS)
OMIM ID 243605
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2015-11-19 00:00:35 +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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00054758 26820108-FamA PubMed: Filges 2016 2-generation family, 2 affected sisters, unaffected heterozygous carrier parents F no Norway Caucasion - - - - STROMS Strømme syndrome CENPF CENPF 2 2 Kaja Selmer
00181108 26820108-FamB PubMed: Filges 2016 2-generation family, 2 affected (F, fetus), unaffected heterozygous carrier parents F ? - - - - - - STROMS Microphthalmia, Xiphoid cleft, Hydronephrosis, duodenal atresia and «apple peel» atresia CENPF CENPF 2 2 Isabel Filges
00181148 26820108-FamB PubMed: Filges 2016 - M ? - - - - - - STROMS Xiphoid cleft (HP:0100891), Renal hypoplasia (HP:0000089), duodenal atresia (HP:0002247), jejunal atresia (HP:0005235) CENPF CENPF 2 1 Isabel Filges
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