OMOP Concept 4035147
Autosomal dominant hypophosphatemic bone disease
StandardConditionSNOMED237890006Disorder
Maps from
1
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal dominant hypophosphatemic bone disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 237890006 | Autosomal dominant hypophosphataemic bone disease | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant hypophosphatemic bone disease across source vocabularies.
- Autosomal dominant hypophosphataemic bone disease
- Autosomal dominant hypophosphatemic bone disease (disorder)
- enfermedad ósea hipofosfatémica autosómica dominante
- enfermedad ósea hipofosfatémica autosómica dominante (trastorno)
- raquitismo hipercalciúrico
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(31)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Developmental hereditary disorder
- 1Dysplasia with defective mineralization
- 1Hereditary disorder of musculoskeletal system
- 1Hypophosphatemia
- 1Lesion of bone
- 1Metabolic bone disease
- 2Autosomal hereditary disorder
- 2Congenital anomaly of skeletal bone
- 2Developmental disorder
- 2Disorder of bone
- 2Disorder of musculoskeletal system
- 2Disorder of phosphorus metabolism
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Metabolic disease
- 2Skeletal dysplasia
- 3Bone finding
- 3Congenital anomaly of musculoskeletal system
- 3Disease
- 3Disorder of body system
- 3Disorder of bone development
- 3Disorder of phosphate, calcium and vitamin D metabolism
- 3Disorder of skeletal system
- 3Genetic disease
Narrower concepts
(2)Included automatically when you query with descendants.
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