SDHB

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

13 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 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