CEMIP

cell migration inducing hyaluronan binding protein
OMIM: 608366, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red CEMIP in Mendeliome


Version 1.3664

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • ClinGen
  • ClinGen
Phenotypes
  • Nonsyndromic genetic hearing loss, MONDO:0019497
Tags
  • disputed

Red CEMIP in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.295

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • ClinGen
Phenotypes
  • Nonsyndromic genetic hearing loss, MONDO:0019497
Tags
  • disputed