tuberous sclerosis 2

Preferred Label : tuberous sclerosis 2;

MeSH note : mutation in TSC2;

Origin ID

C566021;

UMLS CUI

C1860707;

Automatic exact mappings (from CISMeF team)
- TSC complex subunit 2 [ORDO Gene]
- tuberous sclerosis 2 [DO Concept]
Currated CISMeF NLP mapping
- Tuberous Sclerosis 2 [NCIt concept]
- Tuberous sclerosis 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- tuberous sclerosis [MeSH Descriptor]
Record concept(s)
- tuberous sclerosis 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Tuberous Sclerosis 2 [NCIt concept]
- Tuberous sclerosis 2 [OMIM Phenotype]