OMOP Concept 37395877
Reinhardt Pfeiffer mesomelic dysplasia
StandardConditionSNOMED715472000Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Reinhardt Pfeiffer mesomelic dysplasia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537349 | Mesomelic dwarfism Reinhardt Pfeiffer type | Non-standard |
| Nebraska Lexicon | 715472000 | Mesomelic dysplasia of hypoplastic ulna and fibula type | Non-standard |
Synonyms
Alternative names recorded for Reinhardt Pfeiffer mesomelic dysplasia across source vocabularies.
- displasia mesomélica de Reinhardt Pfeiffer
- displasia mesomélicas tipo cúbito y peroné hipoplásicos
- displasia mesomélicas tipo cúbito y peroné hipoplásicos (trastorno)
- Mesomelic dwarfism Reinhardt-Pfeiffer type
- Mesomelic dysplasia of hypoplastic ulna and fibula type
- Mesomelic dysplasia of hypoplastic ulna and fibula type (disorder)
- Reinhardt Pfeiffer syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(54)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital hypoplasia of fibula
- 1Congenital hypoplasia of ulna
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Mesomelic dysplasia
- 1Short stature disorder
- 2Autosomal hereditary disorder
- 2Congenital anomaly of fibula
- 2Congenital anomaly of skeletal bone
- 2Congenital anomaly of ulna
- 2Congenital dysplasia of limb
- 2Congenital hypoplasia of part of upper limb
- 2Congenital malformation syndrome
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Disorder of stature
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hypoplasia of lower limb
- 2Skeletal dysplasia
- 3Congenital anomaly of limb
- 3Congenital anomaly of lower limb
- 3Congenital anomaly of musculoskeletal system
- 3Congenital anomaly of upper limb
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