Kenny-Caffey syndrome, type 1

Preferred Label : Kenny-Caffey syndrome, type 1;

MeSH synonym : Kenny-Caffey syndrome, autosomal recessive form; Kenny-Caffey syndrome, autosomal recessive;

MeSH Hyperonym : Kenny syndrome;

Details

Origin ID

C537021;

UMLS CUI

C1855648;

Automatic exact mappings (from CISMeF team)
- Kenny syndrome (disorder) [SNOMED CT concept]
- Kenny-Caffey syndrome [ORDO Disease]
- Kenny-Caffey syndrome, autosomal recessive [ICD-11 More detail]
- Kenny-caffey syndrome, type 2 [OMIM Phenotype]
Currated CISMeF NLP mapping
- Autosomal recessive Kenny-Caffey syndrome [ORDO Disease]
- Kenny-Caffey Syndrome Type 1 [NCIt concept]
- Kenny-Caffey syndrome type 1 [DO Concept]
- Kenny-caffey syndrome, type 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- hyperostosis, cortical, congenital [MeSH Descriptor]
Record concept(s)
- Kenny Caffey syndrome [MeSH concept]
- Kenny-Caffey syndrome, Type 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive Kenny-Caffey syndrome [ORDO Disease]
- Kenny-Caffey Syndrome Type 1 [NCIt concept]
- Kenny-caffey syndrome, type 1 [OMIM Phenotype]

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