ciliary dyskinesia, primary, 12

Preferred Label : ciliary dyskinesia, primary, 12;

MeSH note : mutation in RSPH9;

MeSH synonym : CILD12;

Origin ID

C567211;

UMLS CUI

C2675228;

Currated CISMeF NLP mapping
- Ciliary dyskinesia, primary, 12 [OMIM Phenotype]
- primary ciliary dyskinesia 12 [DO Concept]
MeSH term(s) associated for indexing
- ciliary motility disorders [MeSH Descriptor]
Record concept(s)
- ciliary dyskinesia, primary, 12 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ciliary dyskinesia, primary, 12 [OMIM Phenotype]
- primary ciliary dyskinesia 12 [DO Concept]
Validated automatic mappings to NTBT
- Primary ciliary dyskinesia [ORDO Disease]