OMOP Concept 4271706
Multiple malformation syndrome with unusual brain and/or neuromuscular findings
StandardConditionSNOMED64162006Disorder
Maps from
3
Descendants
19
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
3 source codes normalize to Multiple malformation syndrome with unusual brain and/or neuromuscular findings via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 130622 | Foetal akinesia-hypokinesia sequence | Non-standard |
| CIEL | 133713 | Multiple Malformation Syndrome with Unusual Brain and/or Neuromuscular Findings | Non-standard |
| Nebraska Lexicon | 64162006 | Multiple malformation syndrome with unusual brain and/or neuromuscular findings | Non-standard |
Synonyms
Alternative names recorded for Multiple malformation syndrome with unusual brain and/or neuromuscular findings across source vocabularies.
- Multiple malformation syndrome with unusual brain and/or neuromuscular findings (disorder)
- síndrome de malformación múltiple con hallazgos cerebrales Y/O neuromusculares inusuales
- síndrome de malformación múltiple con hallazgos cerebrales Y/O neuromusculares inusuales (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(8)Roll up to these when you need a wider cohort.
Narrower concepts
(19)Included automatically when you query with descendants.
- 1Ataxia-telangiectasia syndrome
- 1Cerebro-oculo-facio-skeletal syndrome
- 1Cohen syndrome
- 1Crooked calf syndrome
- 1Lowe syndrome
- 1Marinesco-Sjögren syndrome
- 1Meckel-Gruber syndrome
- 1Pallister-Hall syndrome
- 1Pena-Shokeir syndrome type I
- 1Prader-Willi-like syndrome
- 1Schinzel-Giedion syndrome
- 1Sjögren-Larsson syndrome
- 1X-linked hydrocephalus syndrome
- 1Zellweger-like syndrome without peroxisomal anomaly
- 1Zellweger syndrome
- 26q16 microdeletion syndrome
- 2CPE-related Prader-Willi-like syndrome
- 2MAGEL2-related Prader-Willi-like syndrome
- 2SIM1-related Prader-Willi-like syndrome
Get this concept via the API
Resolve Multiple malformation syndrome with unusual brain and/or neuromuscular findings - 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/4271706?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card