OMOP Concept 4149584
Holoprosencephaly sequence
StandardConditionSNOMED30915001Disorder
Maps from
21
Descendants
17
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
21 source codes normalize to Holoprosencephaly sequence via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Holoprosencephaly sequence across source vocabularies.
- Familial alobar holoprosencephaly
- holoprosencefalia
- holoprosencefalia alobular familiar
- Holoprosencephaly
- Holoprosencephaly sequence (disorder)
- HPE - Holoprosencephaly
- secuencia de holoprosencefalia
- secuencia de holoprosencefalia (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(11)Roll up to these when you need a wider cohort.
Narrower concepts
(17)Included automatically when you query with descendants.
- 1Agnathia, holoprosencephaly, situs inversus syndrome
- 1Alobar holoprosencephaly
- 1Cebocephaly
- 1Ethmocephalus
- 1Hartsfield syndrome
- 1Holoprosencephaly and postaxial polydactyly syndrome
- 1Holoprosencephaly craniosynostosis syndrome
- 1Holoprosencephaly with caudal dysgenesis syndrome
- 1Holoprosencephaly with nasal pyriformis aperture
- 1Kundrat's syndrome
- 1Lobar holoprosencephaly
- 1Microform holoprosencephaly
- 1Middle interhemispheric variant of holoprosencephaly
- 1Morse Rawnsley Sargent syndrome
- 1Pancreatic agenesis, holoprosencephaly syndrome
- 1Semi-lobar holoprosencephaly
- 1Steinfeld syndrome
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