Disorders of calcium metabolism

Preferred Label : Disorders of calcium metabolism;

ICD-10 exclusion note : hyperparathyroidism (E21.0-E21.3); hungry bone syndrome (E83.81); chondrocalcinosis (M11.1-M11.2);

Diag associé à un acte (%) : 70.3;

CODEXT : 1;

Source : OMS;

Date de début : 01/01/1997;

Do not code with : true;

Details

Origin ID

E835;

UMLS CUI

C0006705;

CISMeF manual mappings
- Familial hypocalciuric hypercalcemia [ORDO Disease]
- Idiopathic hypercalciuria [ORDO Disease]
Currated CISMeF NLP mapping
- Calcium metabolism disorder [MedDRA Preferred Term]
- Calcium metabolism disorders [MedDRA High Level Term]
- Disorder of calcium metabolism (disorder) [SNOMED CT concept]
- Disorders of calcium metabolism [ICD-11 Subcategory]
- Disorders of calcium metabolism [ICD-9 code]
- Disorders of calcium metabolism [ICD-10 Sub-category (who)]
- Familial hypocalciuric hypercalcaemia [MedDRA Preferred Term]
- Hypercalciuria, absorptive, 2 [OMIM Phenotype]
- calcium metabolism disease [DO Concept]
- calcium metabolism disorder [Disease (Nov.)]
- calcium metabolism disorders [MeSH concept]
- calcium metabolism disorders [MeSH Descriptor]
- disorder of calcium metabolism, nos [SNOMED Notion]
- familial hyperparathyroidism [SNOMED Notion]
- hypercalciuria, absorptive, 2 [MeSH concept]
- hypocalciuric hypercalcemia, familial, type 1 [MeSH Supplementary Concept]
DO Cross reference
- calcium metabolism disease [DO Concept]
- familial hypocalciuric hypercalcemia [DO Concept]
- familial hypocalciuric hypercalcemia 1 [DO Concept]
- familial hypocalciuric hypercalcemia 2 [DO Concept]
- familial hypocalciuric hypercalcemia 3 [DO Concept]
Excluded by
- Dietary calcium deficiency [ICD-10 category]
- Other articular cartilage disorders [ICD-10 Sub-category]
- Other hyperparathyroidism [ICD-10 Sub-category]
ICD-10 exclusion(s)
- Familial chondrocalcinosis [ICD-10 Sub-category]
- Hyperparathyroidism, unspecified [ICD-10 Sub-category]
- Other chondrocalcinosis [ICD-10 Sub-category]
- Other hyperparathyroidism [ICD-10 Sub-category]
- Primary hyperparathyroidism [ICD-10 Sub-category]
- Secondary hyperparathyroidism, not elsewhere classified [ICD-10 Sub-category]
Manual NTBT mappings (CISMeF)
- Familial hypocalciuric hypercalcemia type 1 [ORDO Disease]
- Familial hypocalciuric hypercalcemia type 2 [ORDO Disease]
- Familial hypocalciuric hypercalcemia type 3 [ORDO Disease]
Orphanet concepts
- Autosomal recessive infantile hypercalcemia [ORDO Disease]
- Calciphylaxis [ORDO Disease]
- Calciphylaxis cutis [ORDO Disease]
- Disorder of mineral absorption and transport [ORDO Disease]
- Familial hypocalciuric hypercalcemia [ORDO Disease]
- Familial hypocalciuric hypercalcemia type 1 [ORDO Disease]
- Familial hypocalciuric hypercalcemia type 2 [ORDO Disease]
- Familial hypocalciuric hypercalcemia type 3 [ORDO Disease]
- Idiopathic hypercalciuria [ORDO Disease]
- Visceral calciphylaxis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Calcium metabolism disorder [MedDRA Preferred Term]
- Calcium metabolism disorders [MedDRA High Level Term]
- Disorder of calcium metabolism (disorder) [SNOMED CT concept]
- Disorders of calcium metabolism [ICD-9 code]
- Disorders of calcium metabolism [ICD-11 Subcategory]
- Unspecified disorder of calcium metabolism [ICD-9 code]
- calcium metabolism disease [DO Concept]
- calcium metabolism disorder [Disease (Nov.)]
- calcium metabolism disorders [MeSH Descriptor]
- calcium metabolism disorders [MeSH concept]
- disorder of calcium metabolism, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- familial hypocalciuric hypercalcemia 3 [DO Concept]

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