OMOP Concept 4035149
Autosomal recessive hypophosphatemic bone disease
StandardConditionSNOMED237891005Disorder
Maps from
2
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Autosomal recessive hypophosphatemic bone disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C562793 | Hypophosphatemic Rickets with Hypercalciuria, Hereditary | Non-standard |
| Nebraska Lexicon | 237891005 | HHRH - Hereditary hypophosphataemic rickets with hypercalciuria | Non-standard |
Synonyms
Alternative names recorded for Autosomal recessive hypophosphatemic bone disease across source vocabularies.
- Autosomal recessive hypophosphataemic bone disease
- Autosomal recessive hypophosphatemic bone disease (disorder)
- enfermedad ósea hipofosfatémica autosómica recesiva
- enfermedad ósea hipofosfatémica autosómica recesiva (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Disorder with defective osteoid mineralization
- 1Hereditary disorder of musculoskeletal system
- 1Hypophosphatemia
- 2Autosomal hereditary disorder
- 2Disorder of mineral metabolism
- 2Disorder of musculoskeletal system
- 2Disorder of phosphorus metabolism
- 2Hereditary disorder by system
- 2Metabolic bone disease
- 3Disorder of body system
- 3Disorder of bone
- 3Disorder of phosphate, calcium and vitamin D metabolism
- 3Hereditary disease
- 3Metabolic disease
- 3Musculoskeletal finding
- 4Bone finding
- 4Clinical finding
- 4Disease
- 4Disorder of skeletal system
- 4Genetic disease
Narrower concepts
(2)Included automatically when you query with descendants.
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