Disease #03685 (THES2 (trichohepatoenteric syndrome, type 2 (THES-2)), OMIM:614602)

Official abbreviation THES2
Name trichohepatoenteric syndrome, type 2 (THES-2)
OMIM ID 614602
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 9
Phenotype entries for this disease 8
Associated with 1 gene SKIV2L
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

9 entries on 1 page. Showing entries 1 - 9.
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00107763 - PubMed: Fabre 2012 - - no France - - - - - THES2 Syndromic diarrhea/trichohepatoenteric syndrome SKIV2L SKIV2L 2 1 Johan den Dunnen
00107764 - PubMed: Fabre 2012 - - yes - North Africa - - - - THES2 Syndromic diarrhea/trichohepatoenteric syndrome SKIV2L SKIV2L 1 1 Johan den Dunnen
00107765 - PubMed: Fabre 2012 - - yes Turkey - - - - - THES2 Syndromic diarrhea/trichohepatoenteric syndrome SKIV2L SKIV2L 1 1 Johan den Dunnen
00107766 - PubMed: Fabre 2012 - - no France - - - - - THES2 Syndromic diarrhea/trichohepatoenteric syndrome SKIV2L SKIV2L 2 1 Johan den Dunnen
00107767 - PubMed: Fabre 2012 - - yes Turkey - - - - - THES2 Syndromic diarrhea/trichohepatoenteric syndrome SKIV2L SKIV2L 1 1 Johan den Dunnen
00107768 - PubMed: Fabre 2012 - - yes Turkey - - - - - THES2 Syndromic diarrhea/trichohepatoenteric syndrome SKIV2L SKIV2L 1 1 Johan den Dunnen
00444073 - - - F yes (Turkey) - - - - - THES2 congenital diarrhea, developmental delay, hair abnormalities, xerosis SKIV2L SKIV2L 1 1 Murat Ozturk
00444076 - - - M yes (Turkey) - - - - - THES2 congenital diarrhea immunodeficiency, hair abnormalities, hypogammaglobulinemia, facial dysmorphism SKIV2L SKIV2L 1 1 Murat Ozturk
00451484 296779 - - M likely Turkey - - - - - THES2 Abnormality of the liver, Cholestasis, Small for gestational age, Premature birth, Thrombocytopenia, Anemia, Neonatal respiratory distress, Hypoalbuminemia, Hyperglycemia, Meconium ileus SKIV2L SKIV2L 1 1 Andreas Laner
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