OMOP Concept 4122936
Erythrocyte membrane abnormality
StandardConditionSNOMED234409003Disorder
Maps from
1
Descendants
26
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
1 source code normalizes to Erythrocyte membrane abnormality via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 234409003 | Erythrocyte membrane abnormality | Non-standard |
Synonyms
Alternative names recorded for Erythrocyte membrane abnormality across source vocabularies.
- anomalía de la membrana del eritrocito
- anomalía de la membrana del eritrocito (trastorno)
- Erythrocyte membrane abnormality (disorder)
- trastorno de membrana eritrocitaria
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(6)Roll up to these when you need a wider cohort.
Narrower concepts
(26)Included automatically when you query with descendants.
- 1Abnormal cation transport syndrome
- 1Blood group deletion syndrome
- 1Hereditary acanthocytosis
- 1Hereditary elliptocytosis
- 1Hereditary pyropoikilocytosis
- 1Hereditary spherocytosis
- 1Rh deficiency syndrome
- 2Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome
- 2Chorea acanthocytosis syndrome
- 2Hereditary elliptocytosis due to abnormal protein 4.1
- 2Hereditary elliptocytosis due to alpha spectrin defect
- 2Hereditary elliptocytosis due to beta spectrin-ankyrin interaction
- 2Hereditary elliptocytosis due to beta spectrin defect in self-association
- 2Hereditary elliptocytosis due to deficiency of protein 4.1
- 2Hereditary elliptocytosis due to glycophorin C deficiency
- 2Hereditary elliptocytosis with transient poikilocytosis
- 2Hereditary spherocytosis due to beta spectrin defect
- 2Hereditary spherocytosis due to deficiency of protein 4.2
- 2Hereditary spherocytosis due to spectrin deficiency
- 2Homozygous hereditary elliptocytosis
- 2McLeod neuroacanthocytosis syndrome
- 3Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
- 3Mild hereditary spherocytosis due to spectrin deficiency
- 3Severe hereditary spherocytosis due to spectrin deficiency
- 4Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
- 4Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
Get this concept via the API
Resolve Erythrocyte membrane abnormality - 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/4122936?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card