Tuberous sclerosis complex
Description
A rare neurocutaneous disorder characterized by multisystem hamartomas, most commonly involving the skin, brain, kidneys, lungs, eye, and heart, and associated with neuropsychiatric disorders.
Cell Lines
- BCHi026-A
- BCHi026-A-1
- BCHi026-A-1
- BCHi026-A-2
- BCHi026-A-2
- BCHi026-A-3
- BCHi026-A-3
- BCHi026-A-4
- BCHi026-A-4
- BCHi027-A
- BCHi027-A-1
- BCHi027-A-1
- BCHi027-A-2
- BCHi027-A-2
- BCHi027-A-3
- BCHi027-A-3
- BCHi027-A-4
- BCHi027-A-4
- BCHi027-A-5
- BCHi027-A-5
- BCHi027-A-6
- BCHi027-A-6
- BCHi029-A
- BCHi029-B
- BCHi030-A
- BCHi030-B
- BCHi038-A
- BCHi038-A-1
- BCHi038-A-1
- BCHi038-A-2
- BCHi038-A-2
- BCHi038-A-3
- BCHi038-A-3
- BCHi038-A-4
- BCHi038-A-4
- BCHi038-A-5
- BCHi038-A-5
- BCHi038-A-6
- BCHi038-A-6
- EMCi169-A
- EMCi169-B
- EMCi169-C
- EMCi169-D
- EMCi169-E
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.