Disease #05568 (KCTN1 (keratoconus, type 1 (KTCN-1)), OMIM:148300)

Official abbreviation KCTN1
Name keratoconus, type 1 (KTCN-1)
OMIM ID 148300
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 7
Phenotype entries for this disease 7
Associated with 1 gene VSX1
Associated tissues -
Disease features -
Remarks -
Date created 2019-02-14 12:42:52 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00434893 1 PubMed: Fransen et al., 2021 34 candidate genes targeted from 787 independent keratoconus patients and 856 ethnically matched controls, including results from unpublished studies and literature search. 7 patients with EDS gene variants. ? ? Belgium - - - - - EDS, KCTN1 Diagnosis was based on slit-lamp biomicroscopy and tomographic evaluation of the cornea., Hypermobility, fragile skin, easy bruising. COL12A1 COL12A1 1 1 Nassim Louail
00434894 2 PubMed: Fransen et al., 2021 34 candidate genes targeted from 787 independent keratoconus patients and 856 ethnically matched controls, including results from unpublished studies and literature search. 7 patients with EDS gene variants. ? no Belgium - - - - - EDS, KCTN1 Diagnosis was based on slit-lamp biomicroscopy and tomographic evaluation of the cornea, Hypermobility, fragile skin, easy bruising. COL5A1 COL5A1 1 1 Nassim Louail
00434895 3 PubMed: Fransen et al., 2021 34 candidate genes targeted from 787 independent keratoconus patients and 856 ethnically matched controls, including results from unpublished studies and literature search. 7 patients with EDS gene variants. ? no Belgium - - - - - EDS, KCTN1 Diagnosis was based on slit-lamp biomicroscopy and tomographic evaluation of the cornea., Hypermobility, fragile skin, easy bruising. COL5A1 COL5A1 1 1 Nassim Louail
00434896 4 PubMed: Fransen et al., 2021 34 candidate genes targeted from 787 independent keratoconus patients and 856 ethnically matched controls, including results from unpublished studies and literature search. 7 patients with EDS gene variants. ? no Belgium - - - - - EDS, KCTN1 Diagnosis was based on slit-lamp biomicroscopy and tomographic evaluation of the cornea., Hypermobility, fragile skin, easy bruising. TNXB TNXB 1 1 Nassim Louail
00434897 5 PubMed: Fransen et al., 2021 34 candidate genes targeted from 787 independent keratoconus patients and 856 ethnically matched controls, including results from unpublished studies and literature search. 7 patients with EDS gene variants. ? no Belgium - - - - - EDS, KCTN1 Diagnosis was based on slit-lamp biomicroscopy and tomographic evaluation of the cornea., Hypermobility, fragile skin, easy bruising. COL5A1 COL5A1 1 1 Nassim Louail
00434999 6 PubMed: Fransen et al., 2021 34 candidate genes targeted from 787 independent keratoconus patients and 856 ethnically matched controls, including results from unpublished studies and literature search. 7 patients with EDS gene variants. ? no Belgium - - - - - EDS, KCTN1 Diagnosis was based on slit-lamp biomicroscopy and tomographic evaluation of the cornea., Hypermobility, fragile skin, easy bruising. COL5A1 COL5A1 1 1 Nassim Louail
00435000 7 PubMed: Fransen et al., 2021 34 candidate genes targeted from 787 independent keratoconus patients and 856 ethnically matched controls, including results from unpublished studies and literature search. 7 patients with EDS gene variants. ? no Belgium - - - - - EDS, KCTN1 Diagnosis was based on slit-lamp biomicroscopy and tomographic evaluation of the cornea., Hypermobility, fragile skin, easy bruising. COL5A1 COL5A1 1 1 Nassim Louail
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