OMOP Concept 4033902
Dysostosis
StandardConditionSNOMED109420003Disorder
Maps from
2
Descendants
107
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 Dysostosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | D004413 | Dysostoses | Non-standard |
| Nebraska Lexicon | 109420003 | Dysostosis | Non-standard |
Synonyms
Alternative names recorded for Dysostosis across source vocabularies.
- disostosis
- disostosis (trastorno)
- Dysostosis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of skeletal bone
- 1Skeletal dysplasia
- 2Congenital anomaly of musculoskeletal system
- 2Disorder of bone development
- 2Disorder of skeletal system
- 3Congenital malformation
- 3Developmental disorder
- 3Disorder of bone
- 3Disorder of musculoskeletal system
- 4Bone finding
- 4Congenital disease
- 4Disease
- 4Disorder of body system
- 4Musculoskeletal finding
- 5Clinical finding
- 5Disorder of fetus and/or newborn
Narrower concepts
(107)Included automatically when you query with descendants.
- 1Absent radius, anogenital anomalies syndrome
- 1Acrodysostosis
- 1Acrodysplasia scoliosis
- 1Acrofacial dysostosis Catania type
- 1Acrofacial dysostosis Kennedy Teebi type
- 1Acrofacial dysostosis Palagonia type
- 1Acrofacial dysostosis Rodriguez type
- 1Acropectorovertebral dysplasia
- 1Ankylosing vertebral hyperostosis with tylosis syndrome
- 1Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome
- 1Autosomal dominant spondylocostal dysostosis
- 1Bipartite talus
- 1Brachydactyly, short stature, retinitis pigmentosa syndrome
- 1Camptodactyly and tall stature with scoliosis and hearing loss syndrome
- 1Carney complex, trismus, pseudocamptodactyly syndrome
- 1Catel Manzke syndrome
- 1Cerebro-costo-mandibular syndrome
- 1Cerebro-facio-thoracic dysplasia
- 1Congenital hypoplasia of ulna and intellectual disability syndrome
- 1Coxopodopatellar syndrome
- 1Dysostosis of bone of skull
- 1Ectrodactyly polydactyly syndrome
- 1Endocrine-cerebro-osteodysplasia syndrome
- 1Eye defects, arachnodactyly, cardiopathy syndrome
- 1Femur fibula ulna complex
- 1Fibular aplasia and ectrodactyly syndrome
- 1Filippi syndrome
- 1Fuhrmann syndrome
- 1Guttmacher syndrome
- 1Hallux varus, preaxial polysyndactyly syndrome
- 1Heart-hand syndrome Slovenian type
- 1Heart-hand syndrome type 2
- 1Heart-hand syndrome type 3
- 1Holt-Oram syndrome
- 1Imperforate oropharynx, costovertebral anomalies syndrome
- 1Jarcho-Levin syndrome
- 1Karsch Neugebauer syndrome
- 1Klippel-Feil sequence
- 1Long thumb brachydactyly syndrome
- 1Mandibuloacral dysostosis
- 1Mandibulofacial dysostosis with alopecia
- 1Melhem Fahl syndrome
- 1Morava Mehes syndrome
- 1Nail-patella syndrome
- 1Oculootoradial syndrome
- 1Oliver syndrome
- 1Patent ductus arteriosus, bicuspid aortic valve, hand anomaly syndrome
- 1Patterson Stevenson Fontaine syndrome
- 1Pelvic dysplasia, arthrogryposis of lower limbs syndrome
- 1Pelviscapular dysplasia
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