RHO

rhodopsin
OMIM: 180380, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green RHO in Mendeliome


Version 2.0

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Night blindness, congenital stationary, autosomal dominant 1, MIM# 610445
  • Retinitis pigmentosa 4, autosomal dominant or recessive, MIM# 613731

Green RHO in Retinitis pigmentosa


Level 2: Ophthalmological disorders
Version 1.0

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Royal Melbourne Hospital
Phenotypes
  • Retinitis pigmentosa 4, autosomal dominant or recessive, 613731
  • inherited retinal dystrophy MONDO:0019118

Green RHO in Congenital Stationary Night Blindness


Level 2: Ophthalmological disorders
Version 1.0

0 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Royal Melbourne Hospital
Phenotypes
  • Retinitis punctata albescens
  • Retinitis pigmentosa
  • Night blindness, congenital stationary autosomal dominant 1

Red RHO in Congenital nystagmus


Level 2: Ophthalmological disorders
Version 2.0

2 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review Red
  • Royal Melbourne Hospital
  • Victorian Clinical Genetics Services
Phenotypes
  • Night blindness, congenital stationary, autosomal dominant 1, MIM# 610445
  • Retinitis pigmentosa 4, autosomal dominant or recessive, MIM# 613731