OMOP Concept 36716047
Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome
StandardConditionSNOMED721882001Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 721882001 | Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome | Non-standard |
Synonyms
Alternative names recorded for Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome across source vocabularies.
- ATRUS syndrome
- Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome (disorder)
- síndrome de sinostosis radiocubital con trombocitopenia amegacariocítica
- síndrome de sinostosis radiocubital con trombocitopenia amegacariocítica (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(61)Roll up to these when you need a wider cohort.
- 1Amegakaryocytic thrombocytopenia with congenital malformation
- 1Autosomal dominant hereditary disorder
- 1Congenital radioulnar synostosis
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Inherited platelet disorder
- 2Amegakaryocytic thrombocytopenia
- 2Autosomal hereditary disorder
- 2Congenital abnormal fusion of radius
- 2Congenital abnormal fusion of ulna
- 2Congenital malformation syndrome
- 2Congenital thrombocytopenia
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Failure of differentiation of bones of forearm
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hereditary disorder of cellular element of blood
- 2Platelet disorder
- 2Radioulnar synostosis
- 3Congenital anomaly of radius
- 3Congenital anomaly of skeletal bone
- 3Congenital anomaly of ulna
- 3Congenital anomaly of upper limb
- 3Congenital disease
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