OMOP Concept 4021763
Malformation sequence
StandardConditionSNOMED105989001Disorder
Maps from
1
Descendants
44
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Malformation sequence via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 105989001 | Malformation sequence | Non-standard |
Synonyms
Alternative names recorded for Malformation sequence across source vocabularies.
- Malformation sequence (disorder)
- secuencia de anomalía congénita
- secuencia de anomalía congénita (trastorno)
- secuencia de malformación
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(7)Roll up to these when you need a wider cohort.
Narrower concepts
(44)Included automatically when you query with descendants.
- 1Allemann's syndrome
- 1Athyrotic hypothyroidism sequence
- 1Caudal regression syndrome
- 1Exstrophy of urinary bladder sequence
- 1Holoprosencephaly sequence
- 1Immotile cilia syndrome
- 1Jugular lymphatic obstruction sequence
- 1Klippel-Feil sequence
- 1Laterality sequence
- 1Mayer Rokitansky Küster Hauser syndrome
- 1Occult spinal dysraphism sequence
- 2Agnathia, holoprosencephaly, situs inversus syndrome
- 2Alobar holoprosencephaly
- 2Bilateral left-sidedness sequence
- 2Cebocephaly
- 2Covered exstrophy of bladder
- 2Ethmocephalus
- 2Exstrophy of cloaca sequence
- 2Hartsfield syndrome
- 2Holoprosencephaly and postaxial polydactyly syndrome
- 2Holoprosencephaly craniosynostosis syndrome
- 2Holoprosencephaly with caudal dysgenesis syndrome
- 2Holoprosencephaly with nasal pyriformis aperture
- 2Immotile cilia syndrome due to defective radial spokes
- 2Isomerism of right atrial appendage
- 2Kartagener syndrome
- 2Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome
- 2Kundrat's syndrome
- 2Lobar holoprosencephaly
- 2Mayer Rokitansky Küster Hauser syndrome type 1
- 2Mayer-Rokitansky-Küster-Hauser syndrome type 2
- 2Microform holoprosencephaly
- 2Middle interhemispheric variant of holoprosencephaly
- 2Morse Rawnsley Sargent syndrome
- 2Pancreatic agenesis, holoprosencephaly syndrome
- 2Primary ciliary dyskinesia due to transposition of ciliary microtubules
- 2Primary tethered cord syndrome
- 2Rutland ciliary disorientation syndrome
- 2Semi-lobar holoprosencephaly
- 2Split cord malformation
- 2Steinfeld syndrome
- 2Wildervanck syndrome
- 2Young's syndrome
- 3Split spinal cord malformation type I
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