nephronophthisis 7

Preferred Label : nephronophthisis 7;

MeSH note : mutation in GLIS2;

Origin ID

C566930;

UMLS CUI

C1969092;

CISMeF manual mappings
- nephronophthisis type 7 [Disease (Nov.)]
Currated CISMeF NLP mapping
- Nephronophthisis 7 [OMIM Phenotype]
- nephronophthisis 7 [DO Concept]
MeSH term(s) associated for indexing
- kidney diseases, cystic [MeSH Descriptor]
Record concept(s)
- nephronophthisis 7 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Nephronophthisis 7 [OMIM Phenotype]
- nephronophthisis 7 [DO Concept]
- nephronophthisis type 7 [Disease (Nov.)]