Sudden infant death syndrome

Preferred Label : Sudden infant death syndrome;

CISMeF acronym : SIDS;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : SIDS;

Description : Sudden infant death syndrome (SIDS) is a diagnosis of exclusion which should be made only after a thorough autopsy without identification of a specific cause of death (Mage and Donner, 2004). Weese-Mayer et al. (2007) provided a detailed review of genetic factors that have been implicated in SIDS. The authors concluded that SIDS represents more than 1 entity and has a heterogeneous etiology most likely involving several different genetically controlled metabolic pathways.;

Inheritance : ? Autosomal recessive form vs. multifactorial;

Prefixed ID : #272120;

Details

Origin ID

272120;

UMLS CUI

C0038644;

Automatic exact mappings (from CISMeF team)
- IDS wt Allele [NCIt concept]
- SIDS [HPMULTI term]
- Sudden death of infant [ICD-11 More detail]
- death [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- Crib death [MedDRA LLT]
- SIDS [MedDRA LLT]
- SUDDEN INFANT DEATH SYNDROME [WHO-ART Preferred Term]
- Sudden Infant Death [ICNP subject]
- Sudden Infant Death Syndrome [NCIt concept]
- Sudden infant death (event) [SNOMED CT concept]
- Sudden infant death syndrome [PASCAL descriptor]
- Sudden infant death syndrome [ICD-11 Category]
- Sudden infant death syndrome [ICD-9 code]
- Sudden infant death syndrome [ICD-10 category (who)]
- Sudden infant death syndrome [MedDRA Preferred Term]
- Sudden infant death syndrome (finding) [SNOMED CT concept]
- sudden infant death [MeSH Descriptor]
- sudden infant death [MeSH concept]
- sudden infant death syndrome [DO Concept]
- sudden infant death syndrome [Disease (Nov.)]
- sudden infant death syndrome [MedlinePlus Topic]
- sudden infant death syndrome [SNOMED Notion]
DO Cross reference
- sudden infant death syndrome [DO Concept]
Genes related to phenotype
- Sodium voltage-gated channel, alpha subunit 5 [OMIM gene]
HPO term(s)
- Apneic episodes in infancy [HPO term]
- Autosomal recessive inheritance [HPO term]
- Malignant hyperthermia [HPO term]
- Multifactorial inheritance [HPO term]
- Sudden death [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cot death [MedDRA LLT]
- Crib death [MedDRA LLT]
- Death infant sudden [MedDRA LLT]
- SIDS [MedDRA LLT]
- SIDS (Sudden infant death syndrome) [MedDRA LLT]
- SUDDEN INFANT DEATH SYNDROME [WHO-ART Preferred Term]
- Sudden Infant Death Syndrome [NCIt concept]
- Sudden infant death [MedDRA LLT]
- Sudden infant death syndrome [ICD-10 category (who)]
- Sudden infant death syndrome [MedDRA Preferred Term]
- Sudden infant death syndrome [ICD-9 code]
- Sudden infant death syndrome [PASCAL descriptor]
- Sudden infant death syndrome (finding) [SNOMED CT concept]
- sudden infant death [MeSH Descriptor]
- sudden infant death [MeSH concept]
- sudden infant death syndrome [SNOMED Notion]
- sudden infant death syndrome [MedlinePlus Topic]
- sudden infant death syndrome [DO Concept]

Keyword's position in hierarchy(ies) :

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