OMOP Concept 619154
Autosomal recessive Robinow syndrome
StandardConditionSNOMED890237005Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2021
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal recessive Robinow syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535863 | Robinow syndrome, autosomal recessive | Non-standard |
Synonyms
Alternative names recorded for Autosomal recessive Robinow syndrome across source vocabularies.
- Autosomal recessive Robinow syndrome (disorder)
- síndrome de Robinow autosómico recesivo
- síndrome de Robinow autosómico recesivo (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(89)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of rib
- 1Congenital anomaly of spine
- 1Defect of vertebral segmentation
- 1Finding of vertebra
- 1Robinow syndrome
- 1Short stature disorder
- 2Autosomal hereditary disorder
- 2Bone finding
- 2Congenital anomaly of body wall
- 2Congenital anomaly of thoracic cage
- 2Congenital anomaly of vertebral region of back
- 2Congenital malformation of bone of thorax
- 2Congenital malformation of genital organs
- 2Developmental hereditary disorder
- 2Disorder of bone development
- 2Disorder of pelvic region of trunk
- 2Disorder of stature
- 2Disorder of vertebral column
- 2Finding of rib structure
- 2Hereditary disorder of musculoskeletal system
- 2Mesomelic dysplasia
- 2Multiple malformation syndrome with facial-limb defects as major feature
- 2Reproductive system hereditary disorder
- 2Vertebral column finding
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