 Paragangliomas 2; Pgl2
	Paragangliomas 2; Pgl2
Clinical Features
Top most frequent phenotypes and symptoms related to Paragangliomas 2; Pgl2
- Neoplasm
- Hoarse voice
- Cranial nerve paralysis
- Vocal cord paralysis
- Paraganglioma
- Pulsatile tinnitus
- Chemodectoma
- Glomus jugular tumor
- Loss of voice
- Glomus tympanicum paraganglioma
And another 1 symptoms. If you need more information about this disease we can help you.
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.
Alternative names
Paragangliomas 2; Pgl2 Is also known as glomus tumors, familial, 2.
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 2; Pgl2 Recommended genes panels
| Panel Name, Specifity and genes Tested/covered | 
|---|
|  MitoMet®Plus aCGH Analysis. By Baylor Miraca Genetics Laboratories (United States). 
RGS9, RHO, GRK1, RLBP1, RNASEL, BCS1L, RP1, RP2, RP9, RPE65, RPGR, RPL35A, MRPL3, RPS14, RS1, SAG, SARDH, SCO2, SCP2, SDHB	, (...)
 View the complete list with 612 more genes 
Specificity
 1 % 
Genes
 100 % | 
|  SDHAF2 Sequence Analysis. By Baylor Miraca Genetics Laboratories (United States). 
SDHAF2
 
Specificity
 100 % 
Genes
 100 % | 
|  SDHAF2 Deletion/Duplication Analysis. By Baylor Miraca Genetics Laboratories (United States). 
SDHAF2
 
Specificity
 100 % 
Genes
 100 % | 
|  SDHAF2 Comprehensive - Sequence & Deletion/Duplication Analysis. By Baylor Miraca Genetics Laboratories (United States). 
SDHAF2
 
Specificity
 100 % 
Genes
 100 % | 
|  Hereditary Renal Cancer Panel. By Baylor Miraca Genetics Laboratories (United States). 
SDHA, SDHB, SDHC, SDHD, VHL, WT1, CDKN1C, SDHAF2, FLCN, FH, GPC3, MET, PTEN
 
Specificity
 8 % 
Genes
 100 % | 
|  Hereditary Paraganglioma/Pheochromocytoma Panel. By Baylor Miraca Genetics Laboratories (United States). 
SDHA, SDHB, SDHC, SDHD, VHL, SDHAF2, TMEM127, MAX, RET
 
Specificity
 12 % 
Genes
 100 % | 
|  Hereditary Endocrine Cancer Panel. 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 % | 
|  Comprehensive Hereditary Cancer Panel. 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 % | 
You can get up to 91 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM MESH Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE III; CDG3 DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3; DUH3 DEAFNESS, AUTOSOMAL RECESSIVE 15; DFNB15 ABETALIPOPROTEINEMIA; ABL FUMARASE DEFICIENCY; FMRD TYLOSIS WITH ESOPHAGEAL CANCER; TOC