OMOP Concept 4100574
Type 1 lissencephaly
StandardConditionSNOMED253147000Disorder
Maps from
4
Descendants
6
Valid from
31 Jan 2002
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
4 source codes normalize to Type 1 lissencephaly via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 161116 | Lissencephaly, type I | Non-standard |
| HPO | HP_0006818 | 4-layered lissencephaly | Non-standard |
| MeSH | D054221 | Classical Lissencephalies and Subcortical Band Heterotopias | Non-standard |
| Nebraska Lexicon | 253147000 | Type 1 lissencephaly | Non-standard |
Synonyms
Alternative names recorded for Type 1 lissencephaly across source vocabularies.
- Classic lissencephaly
- lisencefalia clásica
- lisencefalia tipo 1
- lisencefalia tipo 1 (trastorno)
- Type 1 lissencephaly (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.
- 1Lissencephaly
- 2Congenital anomaly of brain
- 2Disorder of neuronal migration and differentiation
- 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
(6)Included automatically when you query with descendants.
- 1Isolated lissencephaly type 1 without known genetic defect
- 1Lissencephaly due to LIS1 mutation
- 1Lissencephaly syndrome Norman Roberts type
- 1Lissencephaly type 1 due to doublecortin gene mutation
- 1Miller Dieker syndrome
- 1Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome
Get this concept via the API
Resolve Type 1 lissencephaly - 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/4100574?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card