OMOP Concept 36717212
Autosomal recessive popliteal pterygium syndrome
StandardConditionSNOMED722376008Disorder
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 Autosomal recessive popliteal pterygium syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C564874 | Popliteal Pterygium Syndrome, Lethal Type | Non-standard |
Synonyms
Alternative names recorded for Autosomal recessive popliteal pterygium syndrome across source vocabularies.
- Autosomal recessive popliteal pterygium syndrome (disorder)
- Bartsocas Papas syndrome
- Lethal popliteal pterygium syndrome
- síndrome de pterigión popliteo autosómico recesivo
- síndrome de pterigión popliteo autosómico recesivo (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(44)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Ectodermal dysplasia
- 1Hereditary disorder of the integument
- 1Popliteal pterygium syndrome
- 2Autosomal hereditary disorder
- 2Congenital anomaly of lower limb
- 2Congenital ectodermal defect
- 2Developmental disorder
- 2Disorder of integument
- 2Disorder of knee
- 2Genodermatosis
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple malformation syndrome with limb defect as major feature
- 3Congenital abnormality of lower limb and pelvic girdle
- 3Congenital anomaly of limb
- 3Congenital anomaly of skin
- 3Congenital malformation
- 3Disease
- 3Disorder of body system
- 3Disorder of embryonic structure
- 3Disorder of free lower limb
- 3Disorder of joint region
- 3Disorder of lower limb
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