Kenny-Caffey syndrome, type 2

Preferred Label : Kenny-Caffey syndrome, type 2;

CISMeF synonym : kenny caffey syndrome; kenny syndrome;

MeSH synonym : Dwarfism, cortical thickening of tubular bones, and transient hypocalcemia;

Détails

Origin ID

C537020;

UMLS CUI

C4316787;

Currated CISMeF NLP mapping
- Kenny Caffey syndrome [Disease (Nov.)]
- Kenny syndrome (disorder) [SNOMED CT concept]
- Kenny-Caffey Syndrome Type 2 [NCIt concept]
- Kenny-Caffey syndrome [ORDO Disease]
- Kenny-Caffey syndrome [MedDRA Preferred Term]
- Kenny-Caffey syndrome type 2 [DO Concept]
- Kenny-caffey syndrome, type 2 [OMIM Phenotype]
- kenny syndrome [SNOMED Notion]
DO Cross reference
- Kenny-Caffey syndrome type 2 [DO Concept]
MeSH term(s) associated for indexing
- dwarfism [MeSH Descriptor]
- hyperostosis, cortical, congenital [MeSH Descriptor]
- hypocalcemia [MeSH Descriptor]
ORDO relation(s)
- Kenny-Caffey syndrome [ORDO Disease]
Record concept(s)
- Kenny-Caffey syndrome, type 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant Kenny-Caffey syndrome [ORDO Disease]
- Kenny syndrome (disorder) [SNOMED CT concept]
- Kenny-Caffey Syndrome [NCIt concept]
- Kenny-Caffey Syndrome Type 2 [NCIt concept]
- Kenny-Caffey syndrome [MedDRA Preferred Term]
- Kenny-Caffey syndrome [ORDO Disease]
- Kenny-caffey syndrome, type 2 [OMIM Phenotype]
- kenny syndrome [SNOMED Notion]
Validated automatic mappings to NTBT
- Kenny-Caffey Syndrome [NCIt concept]

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