Disease #05821 (IS1 (scoliosis, idiopathic, susceptibility to, type 1 (IS-1)), OMIM:181800)

Official abbreviation IS1
Name scoliosis, idiopathic, susceptibility to, type 1 (IS-1)
OMIM ID 181800
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 4
Phenotype entries for this disease -
Associated with 1 gene COL3A1
Associated tissues -
Disease features -
Remarks -
Date created 2020-08-26 12:03:07 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00318469 - PubMed: Haller et al., 2015 The variant in this patient is described as being of unknown significance.The technique used was the custom exome panel. - - - - - - - - IS1 - COL3A1 COL3A1 1 1 Raymond Dalgleish
00319341 - PubMed: Haller et al., 2015 The variant in this patient is described as being of unknown significance.The technique used was the custom exome panel. - - - - - - - - IS1 - COL3A1 COL3A1 1 1 Raymond Dalgleish
00319376 - PubMed: Haller et al., 2015 The variant in this patient is described as being of unknown significance.The technique used was the custom exome panel. - - - - - - - - IS1 - COL3A1 COL3A1 1 1 Raymond Dalgleish
00319400 Family 26 PubMed: Baschal et al., 2018 The patient was diagnosed with idiopathic scoliosis.The technique used was whole exome sequencing. - - - - - - - - IS1 - COL5A2 COL5A2 1 1 Raymond Dalgleish
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