SDHB

succinate dehydrogenase complex iron sulfur subunit B
OMIM: 185470, Gene2Phenotype

13 panels

Panel Reviews Mode of inheritance Details
13 panels

Green SDHB in Incidentalome


Version 0.314

review Unknown
Sources
  • Expert Review Green
  • Melbourne Genomics Health Alliance
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green SDHB in Cancer Predisposition_Paediatric


Level 2: Cancer
Version 0.131

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Paragangliomas 4, MIM# 115310

Green SDHB in Mitochondrial disease


Level 2: Metabolic disorders
Version 0.970

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Mitochondrial Flagship
    Phenotypes
    • Mitochondrial complex II deficiency, nuclear type 4, MIM# 619224
    • Complex II deficiency
    • mitochondrial leucoencephalopathy

    Green SDHB in Additional findings_Adult


    Level 2: Screening
    Version 0.166

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance
    Phenotypes
    • Paragangliomas 4, MIM# 115310

    Green SDHB in Leukodystrophy - paediatric


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.318

    Component of the following Super Panels:

  • Leukodystrophy_Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    • Australian Genomcis Health Alliance Leukodystrophy Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Succinate dehydrogenase-deficient leukoencephalopathy
    • Mitochondrial complex II deficiency, nuclear type 4, MIM# 619224
    • Complex II deficiency
    • mitochondrial leucoencephalopathy

    Amber SDHB in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • BabySeq Category B gene
    Phenotypes
    • Hereditary Paraganglioma-Pheochromocytoma Syndromes

    Amber SDHB in Incidentalome_PREGEN_DRAFT


    Version 0.43

    review Unknown
    Sources
    • Expert Review Amber
    • NSW Health Pathology

    Amber SDHB in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.116

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • BabySeq Category B gene
    • Expert Review Amber
    Phenotypes
    • Hereditary Paraganglioma-Pheochromocytoma Syndromes

    Green SDHB in Transplant Co-Morbidity Superpanel


    Level 2: Screening
    Version 0.18

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance
    Phenotypes
    • Paragangliomas 4, MIM# 115310

    Green SDHB in Pituitary Tumour


    Level 2: Cancer Predisposition
    Version 1.1

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review
    • Expert list
    Phenotypes
    • Pituitary tumor, MONDO:0017611
    • Pituitary gland adenoma, MONDO:0006373
    • Hereditary pheochromocytoma-paraganglioma, MONDO:0017366
    • Pheochromocytoma/paraganglioma syndrome 4, MIM#115310

    Green SDHB in Paraganglioma_phaeochromocytoma


    Level 2: Cancer Predisposition
    Version 1.1

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review
    • Expert list
    Phenotypes
    • Paragangliomas 4, MONDO:0007273
    • Pheochromocytoma, MONDO:0008233
    • Hereditary pheochromocytoma-paraganglioma, MONDO:0017366
    • Pheochromocytoma/paraganglioma syndrome 4, MIM#115310

    Green SDHB in Kidney Cancer


    Level 2: Cancer Predisposition
    Version 1.1

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review
    • Expert list
    Phenotypes
    • Renal carcinoma, MONDO:0005206
    • Hereditary pheochromocytoma-paraganglioma, MONDO:0017366
    • Pheochromocytoma/paraganglioma syndrome 4, MIM#115310

    Green SDHB in Gastrointestinal Stromal Tumour


    Level 2: Cancer Predisposition
    Version 1.0

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review
    • Expert list
    Phenotypes
    • Gastrointestinal stromal tumor, MONDO:0011719
    • Hereditary pheochromocytoma-paraganglioma, MONDO:0017366
    • Pheochromocytoma/paraganglioma syndrome 4, MIM#115310