Disease #05788 (EIEE66 (encephalopathy, epileptic, early infantile, type 66 (EIEE66)), OMIM:618067)

Official abbreviation EIEE66
Name encephalopathy, epileptic, early infantile, type 66 (EIEE66)
OMIM ID 618067
Human Phenotype Ontology Project (HPO) HPO
Inheritance AD
Individuals reported having this disease 1
Phenotype entries for this disease 0
Associated with 1 gene PACS2
Associated tissues -
Disease features -
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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00326512 - - - - - - - - - - - EIEE66 - SCN1A SCN1A 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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