HOXA11

homeobox A11
OMIM: 142958, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Amber HOXA11 in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 1.52

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • Radioulnar synostosis with amegakaryocytic thrombocytopenia 1, MM# 605432

Amber HOXA11 in Bone Marrow Failure


Level 2: Haematological disorders
Version 1.114

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Victorian Clinical Genetics Services
    Phenotypes
    • Radioulnar synostosis with amegakaryocytic thrombocytopenia 1, MIM# 605432

    Amber HOXA11 in Mendeliome


    Version 1.2374

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Victorian Clinical Genetics Services
    Phenotypes
    • Radioulnar synostosis with amegakaryocytic thrombocytopenia 1, MIM# 605432

    Red HOXA11 in Skeletal dysplasia

    Level 3: Skeletal dysplasias
    Level 2: Skeletal disorders
    Version 0.305

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Expert Review Red
    • UKGTN
    • Radboud University Medical Center, Nijmegen
    • NHS GMS
    • Expert list
    • Victorian Clinical Genetics Services
    Phenotypes
    • Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 605432

    Amber HOXA11 in Fetal anomalies


    Version 1.314

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 , OMIM #605432

    Green HOXA11 in IBMDx study


    Version 0.35

    review Unknown
    Sources
    • Expert Review Green
    • IBMDx Study
    • Expert Review Amber
    • Victorian Clinical Genetics Services
    Phenotypes
    • Radioulnar synostosis with amegakaryocytic thrombocytopenia 1, MIM# 605432