Disease #04301 (FANCT (Fanconi anemia, complementation group T (FANCT)), OMIM:616435)

Official abbreviation FANCT
Name Fanconi anemia, complementation group T (FANCT)
OMIM ID 616435
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene UBE2T
Associated tissues -
Disease features -
Remarks -
Date created 2015-07-19 11:41:26 +02:00 (CEST)
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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00046580 - PubMed: Hira 2015; Journal: Hira 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents F no Japan - >25y - - - FANCT see paper; FA phenotype, malformations, hematological abnormalities (hematopoietic stem cell transplantation), chromosome fragility lymphocytes, ... LGR6, UBE2T LGR6, UBE2T 2 1 Johan den Dunnen
00046581 - PubMed: Hira 2015; Journal: Hira 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Japan - 08y - - - FANCT see paper; FA phenotype, malformations, hematological abnormalities (hematopoietic stem cell transplantation), chromosome fragility lymphocytes, ... UBE2T UBE2T 2 1 Johan den Dunnen
00047511 - PubMed: Rickman 2015, Journal: Rickman 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents M no - - - - - - FANCT see paper; at birth bilateral radial aplasia, absent thumbs, microcephaly, micrognathia, cafe au lait spots, absent left kidney, elevated chromosomal breakage in peripheral blood samples treated with DEB, ... - UBE2T 2 1 Francis Lach
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