autoimmune lymphoproliferative syndrome, type IA

Preferred Label : autoimmune lymphoproliferative syndrome, type IA;

MeSH note : mutation in FAS gene;

MeSH synonym : ALPS1A;

Origin ID

C566613;

UMLS CUI

C1866119;

Automatic exact mappings (from CISMeF team)
- Autoimmune lymphoproliferative syndrome [OMIM Phenotype]
- FAS wt Allele [NCIt concept]
- Fas Cell Surface Death Receptor Measurement [NCIt concept]
Currated CISMeF NLP mapping
- Autoimmune Lymphoproliferative Syndrome with FAS Mutation [NCIt concept]
- autoimmune lymphoproliferative syndrome type Ia [Disease (Nov.)]
MeSH term(s) associated for indexing
- autoimmune lymphoproliferative syndrome [MeSH Descriptor]
Record concept(s)
- autoimmune lymphoproliferative syndrome, type IA [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autoimmune Lymphoproliferative Syndrome with FAS Mutation [NCIt concept]