Cystic fibrosis
Description
A rare, genetic pulmonary disorder characterized by sweat, thick mucus secretions causing multisystem disease, chronic infections of the lungs, bulky diarrhea and short stature.
Cell Lines
- SCVIi112-A
- SCVIi113-A
- BIONi010-C-65
- BIONi010-C-66
- IGGi002-A
- IGGi002-B
- RCMGi001-A
- RCMGi002-A
- RCMGi004-A
- RCMGi004-B
- RCMGi005-A
- RCMGi005-B
- RCMGi007-A
- RCMGi008-A
- RCMGi013-A
- ULBe004-A
- HADe002-A
- INSRMe008-A
- INSRMe009-A
- KCLe003-A
- MHHi002-A
- MHHi003-A
- MHHi004-A
- MHHi005-A
- MUBi002-A
- RGIe156-A
- TNRMCi001-A
- VUBe004-A
Link
For more information, please consult the corresponding entry in Orphanet* .
*Orphanet: an online rare disease and orphan drug data base. Copyright, INSERM 1999. Available on http://www.orpha.net.