PTEN hamartoma tumor syndrome
Description
A group of clinically heterogeneous disorders united by a germline PTEN mutation and the involvement of derivatives of all 3 germ cell layers, manifesting with hamartomas, overgrowth and neoplasia. Currently, subsets carrying clinical diagnoses of Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, Proteus and Proteus-like syndromes and SOLAMEN syndrome belong to PHTS.
Cell Lines
- BCHi013-A
- BCHi013-A-1
- BCHi013-A-1
- BCHi013-A-2
- BCHi013-A-2
- BCHi013-A-3
- BCHi013-A-3
- BCHi013-A-4
- BCHi013-A-4
- BCHi014-A
- BCHi014-A-1
- BCHi014-A-1
- BCHi014-A-2
- BCHi014-A-2
- BCHi014-A-3
- BCHi014-A-3
- BCHi014-A-4
- BCHi014-A-4
- BCHi014-A-5
- BCHi014-A-5
- BCHi014-A-6
- BCHi014-A-6
- BCHi014-A-7
- BCHi014-A-7
- BCHi014-A-8
- BCHi014-A-8
- BCHi015-A
- BCHi015-A-1
- BCHi015-A-1
- BCHi015-A-2
- BCHi015-A-2
- BCHi015-A-3
- BCHi015-A-3
- BCHi015-A-4
- BCHi015-A-4
- BCHi015-A-5
- BCHi015-A-5
- BCHi015-A-6
- BCHi015-A-6
- BCHi016-A
- BCHi016-A-1
- BCHi016-A-1
- BCHi016-A-2
- BCHi016-A-2
- BCHi016-A-3
- BCHi016-A-3
- BCHi016-A-4
- BCHi016-A-4
- BCHi017-A
- BCHi017-A-1
- BCHi017-A-1
- BCHi017-A-2
- BCHi017-A-2
- BCHi017-A-3
- BCHi017-A-3
- BCHi017-A-4
- BCHi017-A-4
- BCHi017-A-5
- BCHi017-A-5
- BCHi017-A-6
- BCHi017-A-6
- BCHi018-A
- BCHi018-A-1
- BCHi018-A-1
- BCHi018-A-2
- BCHi018-A-2
- BCHi018-A-3
- BCHi018-A-3
- BCHi018-A-4
- BCHi018-A-4
- BCHi018-A-5
- BCHi018-A-5
- BCHi018-A-6
- BCHi018-A-6
- BCHi019-A
- BCHi019-A-1
- BCHi019-A-1
- BCHi019-A-2
- BCHi019-A-2
- BCHi019-A-3
- BCHi019-A-3
- BCHi019-A-4
- BCHi019-A-4
- BCHi019-A-5
- BCHi019-A-7
- BCHi019-A-7
- BCHi020-A-1
- BCHi020-A-2
- BCHi020-A-3
- BCHi020-A-4
- BCHi042-A
- BCHi019-A-5
- BCHi020-A
- BCHi020-A-1
- BCHi020-A-2
- BCHi020-A-3
- BCHi020-A-4