HBB

hemoglobin subunit beta
OMIM: 141900, Gene2Phenotype

9 panels

Panel Reviews Mode of inheritance Details
9 panels

Green HBB in Mendeliome


Version 1.1891

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Delta-beta thalassemia 141749
  • Erythrocytosis 6 617980
  • Heinz body anemia 140700
  • Hereditary persistence of fetal hemoglobin 141749
  • Methemoglobinemia, beta type 617971
  • Sickle cell anemia 603903
  • Thalassemia-beta, dominant inclusion-body 603902
  • Thalassemia, beta 613985

Green HBB in Mackenzie's Mission_Reproductive Carrier Screening


Level 2: Screening
Version 0.109

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Thalassemias, beta-, 613985 (3)

Green HBB in Stroke


Level 2: Neurology and neurodevelopmental disorders
Version 1.16

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Sickle cell anemia MIM#603903
Tags
  • SV/CNV

Amber HBB in Cerebral vascular malformations


Level 2: Neurology and neurodevelopmental disorders
Version 0.39

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Genomics England PanelApp
    • Expert Review Amber
    Phenotypes
    • Sickle cell anemia 603903

    Green HBB in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • BabySeq Category A gene
    • Expert Review Green
    Phenotypes
    • Beta-thalassemia

    Green HBB in Red cell disorders


    Level 2: Haematological disorders
    Version 1.24

    review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Yorkshire and North East GLH
    • NHS GMS
    • Wessex and West Midlands GLH
    • North West GLH
    • London South GLH
    Phenotypes
    • Thalassemia, beta, MIM# 613985
    • Sickle cell anaemia, MIM# 603903
    • Methaemoglobinaemia, beta type, MIM# 617971
    • Hereditary persistence of fetal haemoglobin, MIM# 141749
    • Heinz body anaemia, MIM# 140700
    • Erythrocytosis 6, MIM# 617980

    Green HBB in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Thalassemias, beta-, 613985 (3)

    Green HBB in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.113

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category A gene
    Phenotypes
    • Sickle cell anaemia, MIM# 603903
    Tags
    • treatable
    • haematological

    Green HBB in Prepair 500+


    Level 2: Screening
    Version 1.1

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Thalassemias, beta-, 613985 (3)