KBG syndrome - CISMeF

Preferred Label : KBG syndrome;

ICD-11 definition : KBG syndrome is a rare malformation syndrome characterised by a typical facial dysmorphism, macrodontia of the upper central incisors, skeletal (mainly costovertebral) anomalies and developmental delay.;

Details

Origin ID

465550090;

Automatic exact mappings (from CISMeF team)
- KBG syndrome [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- KBG syndrome [MeSH Supplementary Concept]
- KBG syndrome [DO Concept]
- KBG syndrome [MeSH concept]
- KBG syndrome [ORDO Disease]
- KBG syndrome [Disease (Nov.)]
- Kbg syndrome [OMIM Phenotype]
- Short stature, facial and skeletal anomalies, intellectual disability, macrodontia syndrome (disorder) [SNOMED CT concept]

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