OMOP Concept 45765628
Congenital brain aplasia
StandardConditionSNOMED702611008Disorder
Maps from
15
Descendants
44
Valid from
31 Jul 2014
Valid to
31 Dec 2099
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Source codes that map to this concept
15 source codes normalize to Congenital brain aplasia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 127772 | Reduction deformities of brain | Non-standard |
| ICD9CM | 742.2 | Congenital reduction deformities of brain | Non-standard |
| Nebraska Lexicon | 204032005 | Reduction deformities of brain | Non-standard |
| Nebraska Lexicon | 702611008 | Brain aplasia, congenital | Non-standard |
| Read | P22..00 | Reduction deformities of brain | Non-standard |
| Read | P220.00 | Agenesis of brain, part unspecified | Non-standard |
| Read | P221.00 | Aplasia of brain, part unspecified | Non-standard |
| Read | P222.00 | Hypoplasia of brain, part unspecified | Non-standard |
| Read | P22y.00 | Other specified reduction deformities of brain | Non-standard |
| Read | P22yz00 | Other reduction deformity of brain NOS | Non-standard |
| Read | P22z.00 | Reduction deformities of brain NOS | Non-standard |
| Read | P22z.12 | Agenesis of part of brain NEC | Non-standard |
| Read | P22z.13 | Hypoplasia of part of brain NEC | Non-standard |
| Read | P22z.14 | Aplasia of part of brain NEC | Non-standard |
| Read | Pyu0200 | [X]Other reduction deformities of brain | Non-standard |
Synonyms
Alternative names recorded for Congenital brain aplasia across source vocabularies.
- aplasia congénita de cerebro
- aplasia congénita de cerebro (trastorno)
- Brain aplasia, congenital
- Congenital brain aplasia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(20)Roll up to these when you need a wider cohort.
- 1Anencephalus
- 2Amyelencephalus
- 2Congenital anomaly of brain
- 3Congenital anomaly of central nervous system
- 3Congenital anomaly of head
- 3Disorder of brain
- 4Congenital anomaly of nervous system
- 4Congenital malformation
- 4Disorder of head
- 4Disorder of the central nervous system
- 4Finding of brain
- 5Central nervous system finding
- 5Congenital disease
- 5Developmental disorder
- 5Disease
- 5Disorder of nervous system
- 5Head finding
- 6Clinical finding
- 6Disorder of body system
- 6Disorder of fetus and/or newborn
Narrower concepts
(44)Included automatically when you query with descendants.
- 1Agenesis of cerebrum
- 1Aplasia of cerebellum
- 1Aplasia of corpus callosum
- 1Congenital agenesis of brainstem nuclei
- 1Hemispheric cerebral agenesis
- 1Isolated arhinencephaly
- 1Partial absence of septum pellucidum
- 2Agenesis of cerebellum
- 2Agenesis of corpus callosum
- 2Agenesis of left hemisphere of cerebellum
- 2Agenesis of right hemisphere of cerebellum
- 2Aicardi's syndrome
- 2Aplasia of the vermis
- 2Congenital aplasia of septum pellucidum
- 2Curry Jones syndrome
- 2Hemispheric cerebellar agenesis
- 2Partial agenesis of corpus callosum
- 2Temtamy syndrome
- 3Acrocallosal syndrome
- 3Agenesis of corpus callosum and abnormal genitalia syndrome
- 3Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome
- 3Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome
- 3Agenesis of corpus callosum with lipoma
- 3Cerebellum agenesis with hydrocephaly
- 3Complete agenesis of vermis
- 3Familial aplasia of the vermis
- 3Infantile osteopetrosis with neuroaxonal dysplasia syndrome
- 3Isolated agenesis of cerebellar vermis
- 3Microcephaly, polymicrogyria, corpus callosum agenesis syndrome
- 3Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome
- 3Permanent neonatal diabetes mellitus with cerebellar agenesis syndrome
- 3Rhombencephalosynapsis
- 3Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome
- 3Vici syndrome
- 3X-linked cerebral, cerebellar, coloboma syndrome
- 3X-linked lissencephaly with abnormal genitalia syndrome
- 4Gomez Lopez Hernandez syndrome
- 4Joubert syndrome
- 5Joubert syndrome with congenital hepatic fibrosis
- 5Joubert syndrome with Jeune asphyxiating thoracic dystrophy
- 5Joubert syndrome with ocular defect
- 5Joubert syndrome with oculorenal defect
- 5Joubert syndrome with orofaciodigital defect
- 5Joubert syndrome with renal defect
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