KY

kyphoscoliosis peptidase
OMIM: 605739, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green KY in Congenital myopathy


Level 2: Neurology
Version 6.45
Latest signed off version: v6.0 (30 Apr 2025)

Component of the following Super Panels:

  • Hypotonic infant
  • Other rare neuromuscular disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    • UCL
    Phenotypes
    • Myopathy, myofibrillar, 7, OMIM:617114