Senior-Loken syndrome 6

Preferred Label : Senior-Loken syndrome 6;

MeSH note : mutation in NPHP6;

Origin ID

C565708;

UMLS CUI

C1857779;

Currated CISMeF NLP mapping
- Senior-loken syndrome 6 [OMIM Phenotype]
MeSH term(s) associated for indexing
- Ciliopathies [MeSH Descriptor]
- kidney diseases, cystic [MeSH Descriptor]
- leber congenital amaurosis [MeSH Descriptor]
- optic atrophies, hereditary [MeSH Descriptor]
Record concept(s)
- Senior-Loken syndrome 6 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Senior-loken syndrome 6 [OMIM Phenotype]