PBXIP1

PBX homeobox interacting protein 1
ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red PBXIP1 in Mendeliome


Version 1.3936

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • non-syndromic genetic hearing loss, MONDO:0019497, PBXIP1-related

Red PBXIP1 in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.312

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
  • Literature
Phenotypes
  • non-syndromic genetic hearing loss, MONDO:0019497, PBXIP1-related