OMOP Concept 4079975
Congenital malformation
StandardConditionSNOMED276654001Disorder
Maps from
60
Descendants
8,900
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
60 source codes normalize to Congenital malformation via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Congenital malformation across source vocabularies.
- CM - Congenital malformation
- Congenital abnormality
- Congenital anomaly
- Congenital malformation (disorder)
- Fetal developmental abnormality
- Fetal malformation
- Foetal developmental abnormality
- Foetal malformation
- malformación congénita
- malformación congénita (trastorno)
- malformación fetal
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(5)Roll up to these when you need a wider cohort.
Narrower concepts
(8,900)Included automatically when you query with descendants.
- 111p15 duplication syndrome
- 112q15q21.1 microdeletion syndrome
- 113q partial monosomy syndrome
- 115q11.2 microdeletion syndrome
- 115q11q13 microduplication syndrome
- 115q13.3 microdeletion
- 115q13.3 microduplication syndrome
- 116p11.2p12.2 microduplication syndrome
- 116p13.11 microduplication syndrome
- 116q24.1 microdeletion syndrome
- 116q24.3 microdeletion syndrome
- 117q11 deletion syndrome
- 117q23.1-q23.2 duplication syndrome
- 117q24-qter duplication syndrome
- 11p21.3 microdeletion syndrome
- 11p36 deletion syndrome
- 11q21.1 microdeletion
- 120p12.2 deletion syndrome
- 122q13.3 deletion syndrome
- 12q24 microdeletion syndrome
- 13p25.3 deletion syndrome
- 17p12-p14 deletion syndrome
- 17p21.1 deletion syndrome
- 17q31 microdeletion syndrome
- 19p24.3 deletion syndrome
- 19q34 deletion syndrome
- 1Abnormal fetal duplication
- 1Albinism
- 1Alpha-thalassemia intellectual disability syndrome linked to chromosome 16
- 1Bowen-Conradi syndrome
- 1Cat eye syndrome
- 1Chromosome 16p11.2 deletion syndrome
- 1Chromosome 2q37 deletion syndrome
- 1Chromosome Xp11.3 microdeletion syndrome
- 1Common atrioventricular orifice in double inlet ventricle
- 1Complete trisomy 16 syndrome
- 1Complete trisomy 18 syndrome
- 1Complete trisomy 20 syndrome
- 1Complete trisomy 21 syndrome
- 1Complete trisomy 22 syndrome
- 1Congenital abnormality of lower limb and pelvic girdle
- 1Congenital absence of genital tubercle
- 1Congenital anomaly of back
- 1Congenital anomaly of body cavity
- 1Congenital anomaly of body wall
- 1Congenital anomaly of cardiovascular system
- 1Congenital anomaly of craniovertebral junction
- 1Congenital anomaly of digestive system
- 1Congenital anomaly of endocrine gland
- 1Congenital anomaly of head
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