OMOP Concept 37399496
Holoprosencephaly and postaxial polydactyly syndrome
StandardConditionSNOMED716091000Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Holoprosencephaly and postaxial polydactyly syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535829 | Pseudotrisomy 13 syndrome | Non-standard |
Synonyms
Alternative names recorded for Holoprosencephaly and postaxial polydactyly syndrome across source vocabularies.
- Holoprosencephaly and postaxial polydactyly syndrome (disorder)
- Pseudotrisomy 13 syndrome
- síndrome de holoprosencefalia y polidactilia postaxial
- síndrome de holoprosencefalia y polidactilia postaxial (trastorno)
- síndrome de pseudotrisomía 13
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(30)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Holoprosencephaly sequence
- 1Multiple malformation syndrome with facial defects as major feature
- 1Polydactyly
- 2Autosomal hereditary disorder
- 2Congenital anomaly of digit
- 2Congenital anomaly of face
- 2Congenital anomaly of head
- 2Developmental disorder
- 2Hereditary disease
- 2Malformation sequence
- 2Multiple system malformation syndrome
- 2Polymelia
- 3Congenital anomaly of limb
- 3Congenital malformation
- 3Congenital malformation syndrome
- 3Disease
- 3Disorder of digit
- 3Disorder of face
- 3Disorder of head
- 3Genetic disease
- 4Clinical finding
- 4Congenital disease
- 4Disorder of limb
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