hypophosphatasia, nos

Preferred Label : hypophosphatasia, nos;

Détails

Origin ID

D6-95200;

UMLS CUI

C0020630;

Automatic exact mappings (from CISMeF team)
- Disorders of phosphorus metabolism [ICD-10 Sub-category (who)]
- Hypophosphatasia [ICD-11 More detail]
- Infantile hypophosphatasia (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Hypophosphatasia [PASCAL descriptor]
- Hypophosphatasia [NCIt concept]
- Hypophosphatasia [MedDRA Preferred Term]
- Hypophosphatasia [ORDO Disease]
- Hypophosphatasia (disorder) [SNOMED CT concept]
- hypophosphatasia [Disease (Nov.)]
- hypophosphatasia [DO Concept]
- hypophosphatasia [MeSH Descriptor]
- hypophosphatasia [MeSH concept]
ICD-10 exact mapping(s)
- Disorders of phosphorus metabolism [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Developmental anomaly of metabolic origin [ORDO Disease]
- Primary bone dysplasia with defective bone mineralization [ORDO Disease]
- Rare disease with odontological manifestation [ORDO Disease]
Metaterm(s)
- metabolism [CISMeF Metaterm]
Référence SNOMED
- alkaline phosphatase [SNOMED Notion]
- congenital deficiency, nos [SNOMED Notion]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deficiency of alkaline phosphatase (disorder) [SNOMED CT concept]
- Hypophosphatasia [ORDO Disease]
- Hypophosphatasia [MedDRA Preferred Term]
- Hypophosphatasia [PASCAL descriptor]
- Hypophosphatasia [NCIt concept]
- Hypophosphatasia (disorder) [SNOMED CT concept]
- hypophosphatasia [MeSH Descriptor]
- hypophosphatasia [MeSH concept]
- hypophosphatasia [Disease (Nov.)]
- hypophosphatasia [DO Concept]

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

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