autoimmune lymphoproliferative syndrome, type IB

Preferred Label : autoimmune lymphoproliferative syndrome, type IB;

MeSH note : mutation in FASL gene;

MeSH synonym : ALPS1B;

Origin ID

C566614;

UMLS CUI

C1866120;

Currated CISMeF NLP mapping
- Autoimmune Lymphoproliferative Syndrome with Germline FASLG Mutation [NCIt concept]
- autoimmune lymphoproliferative syndrome type Ib [Disease (Nov.)]
MeSH term(s) associated for indexing
- autoimmune lymphoproliferative syndrome [MeSH Descriptor]
Record concept(s)
- autoimmune lymphoproliferative syndrome, type IB [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autoimmune Lymphoproliferative Syndrome with Germline FASLG Mutation [NCIt concept]
- autoimmune lymphoproliferative syndrome type Ib [Disease (Nov.)]