OMOP Concept 606878
Microcephaly
StandardObservationSNOMED1148757008Clinical Finding
Maps from
13
Descendants
124
Valid from
31 Jul 2021
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
13 source codes normalize to Microcephaly via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Microcephaly across source vocabularies.
- microcefalia
- microcefalia (hallazgo)
- Microcephalus
- Microcephaly (finding)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(124)Included automatically when you query with descendants.
- 1Child HC < 0.4th centile
- 1Child HC = 0.4th centile
- 1Child HC 0.5th - 1.9th centile
- 1Child HC = 2nd centile
- 1Christianson syndrome
- 1Congenital ichthyosis, microcephalus, tetraplegia syndrome
- 1Congenital microcephaly
- 1Congenital pontocerebellar hypoplasia type 11
- 1Deficiency of leukotriene C4 synthase
- 1Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome
- 1Fatty acyl-CoA reductase 1 deficiency
- 1Fetal microcephaly
- 1Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
- 1Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome
- 1ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement
- 1Menke Hennekam syndrome
- 1Microcephaly, congenital cataract, psoriasiform dermatitis syndrome
- 1Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome
- 1Microcephaly, thin corpus callosum, intellectual disability syndrome
- 1MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome
- 1PLAA-associated neurodevelopmental disorder
- 1Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome
- 1Progressive cerebello-cerebral atrophy
- 1Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome
- 1PYCR2-related microcephaly, progressive leukoencephalopathy
- 1Sanjad Sakati syndrome
- 1Secondary microcephaly
- 1Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome
- 1Severe neonatal onset encephalopathy with microcephaly
- 1Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract
- 1Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome
- 1USP18 deficiency
- 219p13.3 microduplication syndrome
- 23-phosphoglycerate dehydrogenase deficiency infantile form
- 2Achalasia microcephaly syndrome
- 2Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
- 2AMeD syndrome
- 2Amish lethal microcephaly
- 2Anonychia with microcephaly syndrome
- 2Aphalangy and syndactyly with microcephaly syndrome
- 2Autosomal dominant primary microcephaly
- 2Autosomal recessive chorioretinopathy and microcephaly syndrome
- 2Autosomal recessive primary microcephaly
- 2Cerebellar-facial-dental syndrome
- 2CIMDAG syndrome
- 2Cleft palate, large ears, small head syndrome
- 2Congenital intrauterine infection-like syndrome
- 2Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome
- 2Congenital pontocerebellar hypoplasia type 12
- 2Congenital pontocerebellar hypoplasia type 14
Get this concept via the API
Resolve Microcephaly - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/606878?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card