Bronchiectasis With Or Without Elevated Sweat Chloride 1; Besc1
Genes related to Bronchiectasis With Or Without Elevated Sweat Chloride 1; Besc1
- CFTR
- SCNN1B
Clinical Features
Phenotypes and symptoms related to Bronchiectasis With Or Without Elevated Sweat Chloride 1; Besc1
- Dehydration
- Abnormal lung morphology
- Bronchiectasis
- Sinusitis
- Recurrent pneumonia
- Chronic bronchitis
- Immotile cilia
- Bronchomalacia
- Elevated sweat chloride
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
Bronchiectasis With Or Without Elevated Sweat Chloride 1; Besc1 Is also known as cystic fibrosis-like syndrome.
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.Bronchiectasis With Or Without Elevated Sweat Chloride 1; Besc1 Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
Ashkenazic Genetic Disease Panel.
By Baylor Miraca Genetics Laboratories (United States).
CFTR, HEXA, ELP1, ASPA
Specificity
25 %
Genes
50 % |
CFTR - 5T Variant Analysis.
By Baylor Miraca Genetics Laboratories (United States).
CFTR
Specificity
100 %
Genes
50 % |
CFTR Comprehensive - Sequence & Deletion/Duplication Analysis.
By Baylor Miraca Genetics Laboratories (United States).
CFTR
Specificity
100 %
Genes
50 % |
CFTR Deletion/Duplication Analysis.
By Baylor Miraca Genetics Laboratories (United States).
CFTR
Specificity
100 %
Genes
50 % |
CFTR Sequence Analysis.
By Baylor Miraca Genetics Laboratories (United States).
CFTR
Specificity
100 %
Genes
50 % |
CFTR Sequence Analysis (Familial Mutation/Variant Analysis).
By Baylor Miraca Genetics Laboratories (United States).
CFTR
Specificity
100 %
Genes
50 % |
CFTR Sequence Analysis (Prenatal Diagnosis).
By Baylor Miraca Genetics Laboratories (United States).
CFTR
Specificity
100 %
Genes
50 % |
GeneAware Complete Panel Version 2 (Female).
By Baylor Miraca Genetics Laboratories (United States).
RMRP, BCS1L, SACS, BLM, SGCA, SGCB, SGCG, SGSH, SLC12A6, SLC17A5, SLC22A5, SLC25A13, SLC25A15, SLC26A2, SLC35A3, SLC7A7, SMN1, SMPD1, BTD, BTK , (...)
View the complete list with 139 more genes
Specificity
1 %
Genes
50 % |
You can get up to 306 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 HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH WILSON DISEASE MENTAL RETARDATION, AUTOSOMAL DOMINANT 26; MRD26 GILLES DE LA TOURETTE SYNDROME; GTS FAMILIAL PANCREATIC CARCINOMA
Ashkenazic Genetic Disease Panel.