OMOP Concept 35623622
Hartsfield syndrome
StandardConditionSNOMED766032007Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2018
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Hartsfield syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C564484 | Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate | Non-standard |
| Nebraska Lexicon | 766032007 | Holoprosencephaly, ectrodactyly, cleft lip, cleft palate syndrome | Non-standard |
Synonyms
Alternative names recorded for Hartsfield syndrome across source vocabularies.
- Hartsfield Bixler Demyer syndrome
- Holoprosencephaly, ectrodactyly, cleft lip, cleft palate syndrome
- Holoprosencephaly, ectrodactyly, cleft lip, cleft palate syndrome (disorder)
- síndrome de holoprosencefalia, ectrodactilia y fisura de labio y paladar
- síndrome de holoprosencefalia, ectrodactilia y fisura de labio y paladar (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(26)Roll up to these when you need a wider cohort.
- 1Autosomal hereditary disorder
- 1Developmental hereditary disorder
- 1Ectrodactyly
- 1Holoprosencephaly sequence
- 1Multiple malformation syndrome with limb defect as major feature
- 2Adactyly
- 2Congenital anomaly of head
- 2Developmental disorder
- 2Hereditary disease
- 2Malformation sequence
- 2Multiple system malformation syndrome
- 3Congenital anomaly of digit
- 3Congenital malformation
- 3Congenital malformation syndrome
- 3Disease
- 3Disorder of head
- 3Genetic disease
- 3Partial congenital absence of limb
- 4Clinical finding
- 4Congenital anomaly of limb
- 4Congenital disease
- 4Disorder of digit
- 4Head finding
- 5Disorder of fetus and/or newborn
- 5Disorder of limb
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