OMOP Concept 35622401
Spondyloepimetaphyseal dysplasia Handigodu type
StandardConditionSNOMED763885008Disorder
Maps from
0
Descendants
0
Valid from
31 Jul 2018
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Spondyloepimetaphyseal dysplasia Handigodu type across source vocabularies.
- displasia espondiloepimetafisaria tipo Handigodu
- displasia espondiloepimetafisaria tipo Handigodu (trastorno)
- Spondyloepimetaphyseal dysplasia Handigodu type (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(37)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Spondyloepimetaphyseal disorder
- 2Autosomal hereditary disorder
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Metaphyseal chondrodysplasia
- 3Congenital anomaly of skeletal bone
- 3Congenital malformation syndromes associated with short stature
- 3Disease
- 3Disorder of body system
- 3Genetic disease
- 3Lesion of bone
- 3Musculoskeletal finding
- 3Skeletal dysplasia
- 4Clinical finding
- 4Congenital anomaly of musculoskeletal system
- 4Congenital malformation syndrome
- 4Disorder of bone
- 4Disorder of bone development
- 4Short stature disorder
- 4Structural abnormality of skeleton
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