OMOP Concept 606879
Congenital microcephaly
StandardConditionSNOMED1148758003Disorder
Maps from
11
Descendants
88
Valid from
31 Jul 2021
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
11 source codes normalize to Congenital microcephaly via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 161057 | Microcephaly with normal to thin cortex | Non-standard |
| CIEL | 161060 | Microcephaly with extensive polymicrogyria | Non-standard |
| CIM10 | Q02 | Microcephaly | Non-standard |
| HPO | HP_0011451 | Primary microcephaly | Non-standard |
| ICD10 | Q02 | Microcephaly | Non-standard |
| ICD10CM | Q02 | Microcephaly | Non-standard |
| ICD10CN | Q02 | Microcephaly | Non-standard |
| ICD10CN | Q02.x00 | Microcephaly | Non-standard |
| ICD10GM | Q02 | Microcephaly | Non-standard |
| ICD9CM | 742.1 | Microcephalus | Non-standard |
| KCD7 | Q02 | Microcephaly | Non-standard |
Synonyms
Alternative names recorded for Congenital microcephaly across source vocabularies.
- Congenital microcephalus
- Congenital microcephaly (disorder)
- microcefalia congénita
- microcefalia congénita (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(12)Roll up to these when you need a wider cohort.
Narrower concepts
(88)Included automatically when you query with descendants.
- 119p13.3 microduplication syndrome
- 13-phosphoglycerate dehydrogenase deficiency infantile form
- 1Achalasia microcephaly syndrome
- 1Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
- 1AMeD syndrome
- 1Amish lethal microcephaly
- 1Anonychia with microcephaly syndrome
- 1Aphalangy and syndactyly with microcephaly syndrome
- 1Autosomal dominant primary microcephaly
- 1Autosomal recessive chorioretinopathy and microcephaly syndrome
- 1Autosomal recessive primary microcephaly
- 1Cerebellar-facial-dental syndrome
- 1CIMDAG syndrome
- 1Cleft palate, large ears, small head syndrome
- 1Congenital intrauterine infection-like syndrome
- 1Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome
- 1Congenital pontocerebellar hypoplasia type 14
- 1Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome
- 1DONSON-related microcephaly, short stature, limb abnormalities spectrum
- 1Epilepsy, microcephaly, skeletal dysplasia syndrome
- 1Epiphyseal dysplasia, microcephalus, nystagmus syndrome
- 1Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome
- 1Filippi syndrome
- 1Goldberg Shprintzen megacolon syndrome
- 1Hadziselimovic syndrome
Showing 25 of 88. Retrieve the full set via the API.
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