Keutel syndrome

Preferred Label : Keutel syndrome;

ICD-11 definition : Keutel syndrome is an autosomal recessive developmental anomalies syndrome characterised by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism.;

Détails

Origin ID

1083151379;

Currated CISMeF NLP mapping
- Keutel syndrome [MeSH concept]
- Keutel syndrome [ORDO Disease]
- Keutel syndrome [OMIM Phenotype]
- Keutel syndrome [PASCAL descriptor]
- Keutel syndrome (disorder) [SNOMED CT concept]
- keutel syndrome [MeSH Supplementary Concept]

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