Cowden Syndrome 4; Cws4
Table of contents:
Clinical Features
Phenotypes and symptoms related to Cowden Syndrome 4; Cws4
- Hamartoma
- Renal neoplasm
- Abnormality of the gingiva
- Trichilemmoma
- Abnormality of buccal mucosa
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.Cowden Syndrome 4; Cws4 Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
KLLN.
By Fulgent Genetics Fulgent Genetics (United States).
KLLN
Specificity
100 %
Genes
100 % |
Hereditary Cancer Comprehensive Panel.
By NeoGenomics Laboratories NeoGenomics Laboratories, Inc. (United States).
RUNX1, SDHB, SDHC, SDHD, BMPR1A, BRCA1, BRCA2, STK11, EPCAM, TERC, TERT, TP53, TP53BP1, VHL, WT1, XRCC2, CDH1, CDK4, CDKN2A, CEBPA , (...)
View the complete list with 52 more genes
Specificity
2 %
Genes
100 % |
Tempus xT assay.
By Tempus Labs, Inc. (United States).
BCL6, RIT1, BCL7A, BCR, ROS1, RPL5, RPS15, RPS6KB1, RUNX1, RXRA, BLM, SDHA, SDHB, SDHC, SDHD, SEC23B, SEMA3C, BMPR1A, SF3B1, SRSF2 , (...)
View the complete list with 555 more genes
Specificity
1 %
Genes
100 % |
You can get up to -5 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 IMMUNODEFICIENCY, COMMON VARIABLE, 12; CVID12 MYOPATHY, MYOFIBRILLAR, 5; MFM5 BONE MARROW FAILURE SYNDROME 3; BMFS3 BROOKE-SPIEGLER SYNDROME; BRSS CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA; ARCL3A COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18; COXPD18
KLLN.