Developmental and Epileptic Encephalopathy 28

Preferred Label : Developmental and Epileptic Encephalopathy 28;

NCIt synonyms : Early Infantile Epileptic Encephalopathy 28; DEE28; EIEE28;

NCIt definition : An autosomal recessive subtype of developmental and epileptic encephalopathy caused by mutation(s) in the WWOX gene, encoding WW domain-containing oxidoreductase.;

Détails

Origin ID

C189273;

UMLS CUI

C4015519;

Currated CISMeF NLP mapping
- Developmental and epileptic encephalopathy 28 [OMIM Phenotype]
- developmental and epileptic encephalopathy 28 [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 28 [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
- WWOX Gene [NCIt concept]

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

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