Disorders of phosphorus metabolism and phosphatases

Preferred Label : Disorders of phosphorus metabolism and phosphatases;

ICD-10 exclusion note : osteoporosis (M80.-); adult osteomalacia (M83.-);

Diag associé à un acte (%) : 74.7;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E833;

UMLS CUI

C2874300;

Currated CISMeF NLP mapping
- Disorders of phosphorus metabolism or phosphatases [ICD-11 Subcategory]
- phosphorus metabolism disorder [Disease (Nov.)]
Excluded by
- Adult osteomalacia [ICD-10 category]
- Rickets, active [ICD-10 Sub-category]
ICD-10 exclusion(s)
- Adult osteomalacia [ICD-10 category]
- Osteoporosis with current pathological fracture [ICD-10 category]
- Osteoporosis without current pathological fracture [ICD-10 category]
Orphanet concepts
- Adult hypophosphatasia [ORDO Disease]
- Autosomal dominant hypophosphatemic rickets [ORDO Disease]
- Autosomal recessive hypophosphatemic rickets [ORDO Disease]
- Childhood-onset hypophosphatasia [ORDO Disease]
- Disorder of mineral absorption and transport [ORDO Disease]
- Hereditary hypophosphatemic rickets with hypercalciuria [ORDO Disease]
- Hypocalcemic vitamin D-resistant rickets [ORDO Disease]
- Hypophosphatasia [ORDO Disease]
- Hypophosphatemic rickets [ORDO Disease]
- Infantile hypophosphatasia [ORDO Disease]
- Lysosomal acid phosphatase deficiency [ORDO Disease]
- Odontohypophosphatasia [ORDO Disease]
- Perinatal lethal hypophosphatasia [ORDO Disease]
- Prenatal benign hypophosphatasia [ORDO Disease]
- X-linked hypophosphatemia [ORDO Disease]
Semantic type(s)
- Pathologic Function [UMLS semantic type]
Validated automatic mappings to BTNT
- Disorder of phosphorus metabolism (disorder) [SNOMED CT concept]
- Disorders of phosphorus metabolism [ICD-9 code]
- Hypophosphatasia [NCIt concept]
- Phosphorus Metabolic Disorder [NCIt concept]
- Phosphorus metabolism disorder [MedDRA Preferred Term]
- Phosphorus metabolism disorders [MedDRA High Level Term]
- acid phosphatase deficiency [MeSH concept]
- acid phosphatase deficiency [MeSH Supplementary Concept]
- familial hypophosphatemic rickets [MeSH Descriptor]
- hypophosphatasia [MeSH Descriptor]
- hypophosphatasia [MeSH concept]
- hypophosphatemia, familial [MeSH Descriptor]
- hypophosphatemia, familial [MeSH concept]
- phosphorus metabolism disorders [MeSH Descriptor]
- phosphorus metabolism disorders [MeSH concept]
Validated automatic mappings to NTBT
- Hypophosphatasia [ORDO Disease]

Keyword's position in hierarchy(ies) :

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