Pierson syndrome

Preferred Label : Pierson syndrome;

ICD-11 definition : Pierson syndrome is a genetic disorder characterised by the association of congenital nephrotic syndrome with diffuse mesangial sclerosis and ocular anomalies with microcoria.;

Détails

Origin ID

555082533;

Currated CISMeF NLP mapping
- Pierson Syndrome [NCIt concept]
- Pierson syndrome [ORDO Disease]
- Pierson syndrome [DO Concept]
- Pierson syndrome [OMIM Phenotype]
- Pierson syndrome [MeSH concept]
- Pierson syndrome (disorder) [SNOMED CT concept]
- pierson syndrome [MeSH Supplementary Concept]

Position du mot-clé dans l'(les) arborescence(s) :

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