Paragangliomas 4; Pgl4

Clinical Features

Top most frequent phenotypes and symptoms related to Paragangliomas 4; Pgl4

  • Neoplasm
  • Pain
  • Hypertension
  • Congestive heart failure
  • Headache
  • Hyperhidrosis
  • Carcinoma
  • Anxiety
  • Tachycardia
  • Palpitations

And another 16 symptoms. If you need more information about this disease we can help you.

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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 4; Pgl4 Is also known as paraganglioma, familial malignant, pheochromocytoma, extraadrenal, and cervical paraganglioma, carotid body tumors and multiple extraadrenal pheochromocytomas, pheochromocytoma, familial extraadrenal, paragangliomas, hereditary extraadrenal.

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.


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Paragangliomas 4; Pgl4 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
MitoMetĀ®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
50 %
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
50 %
Hereditary Paraganglioma/Pheochromocytoma Panel.

By Baylor Miraca Genetics Laboratories (United States).

SDHA, SDHB, SDHC, SDHD, VHL, SDHAF2, TMEM127, MAX, RET
Specificity
12 %
Genes
50 %
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
50 %
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
50 %
SDHB DNA Sequencing Test.

By Athena Diagnostics Inc (United States).

SDHB
Specificity
100 %
Genes
50 %
Pheochromocytoma Evaluation.

By Athena Diagnostics Inc (United States).

SDHB, VHL, RET
Specificity
34 %
Genes
50 %
Paragangliomas 4.

By Center for Human Genetics, Inc (United States).

SDHB
Specificity
100 %
Genes
50 %

We have 169 more panels available in our App

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like MIRAGE SYNDROME; MIRAGE HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2 FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY; FBP1D EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54; EIEE54 HAND-FOOT-GENITAL SYNDROME; HFG CEROID LIPOFUSCINOSIS, NEURONAL, 11; CLN11 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR

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