PDE1C

phosphodiesterase 1C
OMIM: 602987, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red PDE1C in Mendeliome


Version 1.4516

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

Red PDE1C in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.332

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