CPD

carboxypeptidase D
OMIM: 603102, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red CPD in Intellectual disability


Level 2: Developmental disorders
Version 11.1
Latest signed off version: v11.0 (12 Aug 2026)

Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders
  • review Not set
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services