KLK15:Ensemblv90

kallikrein related peptidase 15
OMIM: 610601, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red KLK15 in Aortopathy_Connective Tissue Disorders


Level 2: Cardiovascular disorders
Version 1.101

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Other
Phenotypes
  • hypermobile Ehlers-Danlos syndrome MONDO:0007523

Red KLK15 in Mendeliome


Version 1.3802

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Other
Phenotypes
  • hypermobile Ehlers-Danlos syndrome MONDO:0007523

Red KLK15 in Aortopathy_Connective Tissue Disorders


Level 2: Cardiovascular disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Other
  • Expert Review Red
Phenotypes
  • hypermobile Ehlers-Danlos syndrome MONDO:0007523