CPD:Ensemblv90

carboxypeptidase D
OMIM: 603102, ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green CPD in Mendeliome


Version 1.3802

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

Green CPD in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.304

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

Green CPD in Deafness_Isolated


Level 2: Hearing and ear disorders
Version 1.84

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

Green CPD in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 2.0

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

Green CPD in Deafness_Isolated


Level 2: Hearing and ear disorders
Version 2.0

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