LOXHD1

lipoxygenase homology PLAT domains 1
OMIM: 613072, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green LOXHD1 in Mendeliome


Version 2.636

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, autosomal recessive 77, MIM# 613079

Green LOXHD1 in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 2.11

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Melbourne Genomics Health Alliance Deafness Flagship
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, autosomal recessive 77, MIM# 613079

Red LOXHD1 in Prepair 1000+


Level 2: Screening
Version 3.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Deafness, autosomal recessive 77 (MIM#613079)

Green LOXHD1 in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 2.13

3 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • BabySeq Category A gene
Phenotypes
  • Deafness, autosomal recessive 77, MIM# 613079
Tags
  • deafness