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 |
---|
![]() By Baylor Miraca Genetics Laboratories (United States).
CFTR, HEXA, ELP1, ASPA
Specificity
25 %
Genes
50 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
CFTR
Specificity
100 %
Genes
50 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
CFTR
Specificity
100 %
Genes
50 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
CFTR
Specificity
100 %
Genes
50 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
CFTR
Specificity
100 %
Genes
50 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
CFTR
Specificity
100 %
Genes
50 % |
![]() By Baylor Miraca Genetics Laboratories (United States).
CFTR
Specificity
100 %
Genes
50 % |
![]() 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 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA DYSTONIA 11, MYOCLONIC; DYT11 ERYTHROLEUKEMIA, FAMILIAL MYHRE SYNDROME; MYHRS STORMORKEN SYNDROME; STRMK MUENKE SYNDROME; MNKES