TBX19

T-box 19
OMIM: 604614, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green TBX19 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Adrenocorticotropic hormone deficiency, 201400

Green TBX19 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • Expert list
    Phenotypes
    • Adrenocorticotropic hormone deficiency - 201400

    Green TBX19 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
    • Adrenocorticotropic hormone deficiency, 201400 (3)

    Green TBX19 in Pituitary hormone deficiency


    Level 2: Endocrine disorders
    Version 0.34

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Adrenocorticotropic hormone deficiency (201400)

    Green TBX19 in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Adrenocorticotropic hormone deficiency, 201400 (3)

    Green TBX19 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.114

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BeginNGS
    Phenotypes
    • Adrenocorticotropic hormone deficiency, MIM#201400
    Tags
    • treatable
    • endocrine