PanelApp (staging)
  1. Genes and Genomic Entities
  2. BLVRA

BLVRA

biliverdin reductase A
OMIM: 109750, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber BLVRA in Mendeliome


Version 1.2302

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Hyperbiliverdinaemia , MIM#614156

Amber BLVRA in Haem degradation and bilirubin metabolism defects


Level 2: Metabolic disorders
Version 0.17

Component of the following Super Panels:

  • Liverome Superpanel
  • Metabolic Disorders Superpanel

    		•  0 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    Phenotypes
    • Disorders of haem degradation and bilirubin metabolism
    • hyperbiliverdinemia MONDO:0013595