OMOP Concept 36713481
Goldblatt syndrome
StandardConditionSNOMED717823001Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Goldblatt syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535792 | Spondylometaphyseal dysplasia with dentinogenesis imperfecta | Non-standard |
| Nebraska Lexicon | 717823001 | Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome | Non-standard |
Synonyms
Alternative names recorded for Goldblatt syndrome across source vocabularies.
- Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome
- Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome (disorder)
- condrodisplasia de Goldblatt
- Goldblatt chondrodysplasia
- Odontochondrodysplasia
- odontocondrodisplasia
- síndrome de condrodisplasia, dentinogénesis imperfecta, laxitud articular
- síndrome de condrodisplasia, dentinogénesis imperfecta, laxitud articular (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(68)Roll up to these when you need a wider cohort.
- 1Congenital dysplasia of limb
- 1Dentinogenesis imperfecta
- 1Hereditary disorder of musculoskeletal system
- 1Metaphyseal chondrodysplasia
- 1Multiple system malformation syndrome
- 2Autosomal dominant hereditary disorder
- 2Congenital anomaly of limb
- 2Congenital anomaly of skeletal bone
- 2Congenital anomaly of tooth
- 2Congenital malformation syndrome
- 2Congenital malformation syndromes associated with short stature
- 2Developmental hereditary disorder
- 2Disorder of hard tissues of teeth
- 2Disorder of musculoskeletal system
- 2Hereditary disorder by system
- 2Hereditary disorder of tooth
- 2Skeletal dysplasia
- 3Autosomal hereditary disorder
- 3Congenital abnormality of oral cavity
- 3Congenital anomaly of digestive organ
- 3Congenital anomaly of jaw
- 3Congenital anomaly of musculoskeletal system
- 3Congenital malformation
- 3Developmental disorder
- 3Digestive system hereditary disorder
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