Developmental and Epileptic Encephalopathy 32

Preferred Label : Developmental and Epileptic Encephalopathy 32;

NCIt synonyms : EIEE32; Early Infantile Epileptic Encephalopathy 32; DEE32;

NCIt definition : An autosomal dominant form of early infantile epileptic encephalopathy, caused by mutation(s) in the KCNA2 gene, encoding potassium voltage-gated channel subfamily A member 2.;

Détails

Origin ID

C155998;

UMLS CUI

C4225350;

Currated CISMeF NLP mapping
- Developmental and epileptic encephalopathy 32 [OMIM Phenotype]
- developmental and epileptic encephalopathy 32 [DO Concept]
Has associated anatomic sites
- Brain [NCIt concept]
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Developmental and epileptic encephalopathy 32 [OMIM Phenotype]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
disease_has_primary_anatomic_site
- Brain [NCIt concept]
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
disease_mapped_to_gene
- KCNA2 Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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