OMOP Concept 4070082
Lissencephaly
StandardConditionSNOMED204036008Disorder
Maps from
10
Descendants
25
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
10 source codes normalize to Lissencephaly via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 116290 | Lissencephaly syndrome | Non-standard |
| CIEL | 149199 | Agyria | Non-standard |
| CIEL | 161059 | Microlissencephaly | Non-standard |
| HPO | HP_0001339 | Lissencephaly | Non-standard |
| HPO | HP_0031882 | Agyria | Non-standard |
| MeSH | D054082 | Lissencephaly | Non-standard |
| Nebraska Lexicon | 204036008 | Lissencephaly pachygyria | Non-standard |
| OXMIS | 7432AG | AGYRIA | Non-standard |
| Read | P223.00 | Agyria | Non-standard |
| Read | P223.11 | Lissencephaly | Non-standard |
Synonyms
Alternative names recorded for Lissencephaly across source vocabularies.
- agiria
- Agyria
- lisencefalia
- lisencefalia (trastorno)
- Lissencephaly (disorder)
- Lissencephaly pachygyria
- Lissencephaly syndrome
- paquigiria lisencefalia
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(19)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of brain
- 1Disorder of neuronal migration and differentiation
- 2Congenital anomaly of central nervous system
- 2Congenital anomaly of head
- 2Disorder of brain
- 3Congenital anomaly of nervous system
- 3Congenital malformation
- 3Disorder of head
- 3Disorder of the central nervous system
- 3Finding of brain
- 4Central nervous system finding
- 4Congenital disease
- 4Developmental disorder
- 4Disease
- 4Disorder of nervous system
- 4Head finding
- 5Clinical finding
- 5Disorder of body system
- 5Disorder of fetus and/or newborn
Narrower concepts
(25)Included automatically when you query with descendants.
- 1Craniotelencephalic dysplasia
- 1Lissencephaly due to TUBA1A (tubulin alpha 1A) mutation
- 1Lissencephaly type 3 metacarpal bone dysplasia syndrome
- 1Lissencephaly with cerebellar hypoplasia
- 1Microlissencephaly
- 1Microlissencephaly micromelia syndrome
- 1Type 1 lissencephaly
- 1Type 2 lissencephaly
- 1Type 3 lissencephaly
- 1X-linked lissencephaly with abnormal genitalia syndrome
- 2Cobblestone lissencephaly without muscular or ocular involvement
- 2Isolated lissencephaly type 1 without known genetic defect
- 2Lissencephaly due to LIS1 mutation
- 2Lissencephaly syndrome Norman Roberts type
- 2Lissencephaly type 1 due to doublecortin gene mutation
- 2Lissencephaly type 3 familial fetal akinesia sequence syndrome
- 2Lissencephaly with cerebellar hypoplasia type A
- 2Lissencephaly with cerebellar hypoplasia type B
- 2Lissencephaly with cerebellar hypoplasia type C
- 2Lissencephaly with cerebellar hypoplasia type D
- 2Lissencephaly with cerebellar hypoplasia type E
- 2Lissencephaly with cerebellar hypoplasia type F
- 2Miller Dieker syndrome
- 2Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome
- 2Walker-Warburg congenital muscular dystrophy
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