Disease #05039 (VUR8 (reflux, vesicoureteral, type 8 (VUR8)), OMIM:615963)

Official abbreviation VUR8
Name reflux, vesicoureteral, type 8 (VUR8)
OMIM ID 615963
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 9
Phenotype entries for this disease -
Associated with 1 gene TNXB
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 11:00:40 +02:00 (CEST)
Date last edited 2020-01-15 08:54:19 +01:00 (CET)


Individuals

9 entries on 1 page. Showing entries 1 - 9.
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00319508 - PubMed: Tokhmafshan et al., 2020 - - - - European (non-Finnish) - - - - VUR8 - TNXB TNXB 1 1 Raymond Dalgleish
00319513 - PubMed: Tokhmafshan et al., 2020 - - - - European (non-Finnish) - - - - VUR8 - TNXB TNXB 1 1 Raymond Dalgleish
00319515 Family 2 PubMed: Gbadegesin et al., 2013 - - - - white - - - - VUR8 - TNXB TNXB 1 1 Raymond Dalgleish
00319518 - PubMed: Tokhmafshan et al., 2020 - - - - - - - - - VUR8 - TNXB TNXB 1 1 Raymond Dalgleish
00319519 - PubMed: Tokhmafshan et al., 2020 - - - - European (non-Finnish) - - - - VUR8 - TNXB TNXB 1 1 Raymond Dalgleish
00319522 - PubMed: Gbadegesin et al., 2013 The variant was described in the published account as ENST00000375244:c.9770C>TThe technique used was whole exome sequencing. - - - white - - - - VUR8 - TNXB TNXB 1 1 Raymond Dalgleish
00319523 - PubMed: Tokhmafshan et al., 2020 - - - - South Asian - - - - VUR8 - TNXB TNXB 1 1 Raymond Dalgleish
00319526 - PubMed: Tokhmafshan et al., 2020 - - - - European (non-Finnish) - - - - VUR8 - TNXB TNXB 1 1 Raymond Dalgleish
00319545 - PubMed: Tokhmafshan et al., 2020 - - - - European (non-Finnish) - - - - VUR8 - TNXB TNXB 1 1 Raymond Dalgleish
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