Paragangliomas 5; Pgl5
Clinical Features
Phenotypes and symptoms related to Paragangliomas 5; Pgl5
- Neoplasm
- Hypertension
- Hyperhidrosis
- Vertigo
- Tachycardia
- Pheochromocytoma
- Paraganglioma
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Paragangliomas 5; Pgl5 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
![]() By Baylor Miraca Genetics Laboratories (United States).
SDHA
Specificity
100 %
Genes
100 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
SDHA
Specificity
100 %
Genes
100 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
SDHA, SDHB, SDHC, SDHD, VHL, WT1, CDKN1C, SDHAF2, FLCN, FH, GPC3, MET, PTEN
Specificity
8 %
Genes
100 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
SDHA, SDHB, SDHC, SDHD, VHL, SDHAF2, TMEM127, MAX, RET
Specificity
12 %
Genes
100 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
SDHA, SDHB, SDHC, SDHD, TP53, VHL, CDC73, SDHAF2, TMEM127, MAX, MEN1, PRKAR1A, PTEN, RET
Specificity
8 %
Genes
100 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
RUNX1, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, STK11, EPCAM, TP53, VHL, WT1, CBL, SUFU, CDC73, CDH1, CDK4, CDKN1C, CDKN2A , (...)
View the complete list with 39 more genes
Specificity
2 %
Genes
100 % |
![]() By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).
BCS1L, SCO1, SCO2, SDHA, SDHB, SDHC, SDHD, SURF1, UQCRB, LRPPRC, NDUFAF5, COX4I2, NDUFA13, ATPAF2, NDUFAF1, NUBPL, NDUFA11, NDUFAF4, PDHX, COX10 , (...)
View the complete list with 35 more genes
Specificity
2 %
Genes
100 % |
![]() By Genetic Services Laboratory University of Chicago (United States).
RUNX1, BLM, SDHA, SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, SRP72, STK11, EPCAM, TERC, TERT, TP53, VHL, IKZF1, SAMD9, SAMD9L, CBL , (...)
View the complete list with 33 more genes
Specificity
2 %
Genes
100 % |
You can get up to 119 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE; THPH2 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4; CHNG4 CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43