focal segmental glomerulosclerosis 5

Preferred Label : focal segmental glomerulosclerosis 5;

MeSH note : mutations in INF2;

Origin ID

C567687;

UMLS CUI

C2750475;

Currated CISMeF NLP mapping
- Focal segmental glomerulosclerosis 5 [OMIM Phenotype]
- focal segmental glomerulosclerosis 5 [DO Concept]
MeSH term(s) associated for indexing
- glomerulosclerosis, focal segmental [MeSH Descriptor]
Record concept(s)
- focal segmental glomerulosclerosis 5 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Focal segmental glomerulosclerosis 5 [OMIM Phenotype]
- focal segmental glomerulosclerosis 5 [DO Concept]