CPD

carboxypeptidase D
OMIM: 603102, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green CPD in Mendeliome


Version 1.3382

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Nonsyndromic genetic hearing loss, MONDO:0019497, CPD-related

Green CPD in Deafness_Isolated


Level 2: Hearing and ear disorders
Version 1.82

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Nonsyndromic genetic hearing loss, MONDO:0019497, CPD-related