OMOP Concept 4308062
Ghosal hematodiaphyseal dysplasia
StandardConditionSNOMED389214003Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Ghosal hematodiaphyseal dysplasia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C565551 | Ghosal Hematodiaphyseal Dysplasia | Non-standard |
Synonyms
Alternative names recorded for Ghosal hematodiaphyseal dysplasia across source vocabularies.
- Diaphyseal dysplasia anaemia syndrome
- Diaphyseal dysplasia anemia syndrome
- Diaphyseal dysplasia with anaemia
- Diaphyseal dysplasia with anemia
- displasia diafisaria y anemia
- displasia hematodiafisaria de Ghosal
- displasia hematodiafisaria de Ghosal (trastorno)
- Ghosal haematodiaphyseal dysplasia
- Ghosal hematodiaphyseal dysplasia (disorder)
- Ghosal syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(55)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anemia
- 1Congenital anomaly of skeletal bone
- 1Developmental hereditary disorder
- 1Dysplasia with increased bone density
- 1Hereditary disorder of cellular element of blood
- 1Hereditary disorder of musculoskeletal system
- 1Lesion of bone
- 1Structural abnormality of diaphysis
- 2Anemia
- 2Autosomal hereditary disorder
- 2Bone density above reference range
- 2Congenital anomaly of musculoskeletal system
- 2Congenital disease
- 2Developmental disorder
- 2Disorder of bone
- 2Disorder of bone development
- 2Disorder of cellular component of blood
- 2Disorder of musculoskeletal system
- 2Hemoglobin below reference range
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Red blood cell count below reference range
- 2Skeletal dysplasia
- 2Structural abnormality of long bone
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