Disease #06187 (EIEE67 (Epileptic encephalopathy, early infantile, 67), OMIM:618141)

Official abbreviation EIEE67
Name Epileptic encephalopathy, early infantile, 67
OMIM ID 618141
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CUX2
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00427665 202469 - - M no Germany - - - - - EIEE67 Talipes equinovarus, Neonatal seizure, Neonatal hypotonia, Temperature instability CUX2 CUX2 1 1 Andreas Laner
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