KLK15

kallikrein related peptidase 15
OMIM: 610601, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 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 1.3741

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