Disease #03404 (EIEE-11 (encephalopathy, epileptic, early infantile, type 11 (EIEE-11)), OMIM:613721)

Official abbreviation EIEE-11
Name encephalopathy, epileptic, early infantile, type 11 (EIEE-11)
OMIM ID 613721
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SCN2A
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Disease features -
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Individuals

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00081086 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - 0 - - EIEE-11 Epileptic encephalopathy, early infantile, 11 (OMIM:613721) SCN2A SCN2A 1 1 Daniel Trujillano
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