CENPP

centromere protein P
OMIM: 611505, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red CENPP in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • autosomal dominant nonsyndromic hearing loss
  • MONDO:0019587

Red CENPP in Deafness_Isolated


Level 2: Hearing and ear disorders
Version 1.63

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • autosomal dominant nonsyndromic hearing loss
  • MONDO:0019587