OMOP Concept 4150135
Dysostosis multiplex group
StandardConditionSNOMED279081001Disorder
Maps from
1
Descendants
15
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Dysostosis multiplex group via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 279081001 | Dysostosis multiplex group | Non-standard |
Synonyms
Alternative names recorded for Dysostosis multiplex group across source vocabularies.
- Dysostosis multiplex group (disorder)
- grupo de disostosis múltiple
- grupo de disostosis múltiple (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(20)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of skeletal bone
- 1Disorder of lysosomal enzyme
- 1Metabolic bone disease
- 1Skeletal dysplasia
- 2Congenital anomaly of musculoskeletal system
- 2Congenital disease
- 2Disorder of bone
- 2Disorder of bone development
- 2Disorder of skeletal system
- 2Enzymopathy
- 2Metabolic disease
- 3Bone finding
- 3Congenital malformation
- 3Developmental disorder
- 3Disease
- 3Disorder of fetus and/or newborn
- 3Disorder of musculoskeletal system
- 4Clinical finding
- 4Disorder of body system
- 4Musculoskeletal finding
Narrower concepts
(15)Included automatically when you query with descendants.
- 1Combined deficiency of sialidase AND beta galactosidase
- 1Dysostosis multiplex
- 1GM1 gangliosidosis
- 1I-cell disease
- 1Mannosidosis
- 1Mucopolysaccharidosis-like plus disease
- 1Sialic storage disease
- 2Adult GM1 gangliosidosis
- 2Infantile GM1 gangliosidosis
- 2Juvenile GM1 gangliosidosis
- 2Mannosidosis, type I
- 2Mannosidosis, type II
- 2Pseudo-Hurler polydystrophy
- 2Salla disease
- 2Sialic acid storage disease, severe infantile type
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