Disease #02197 (EIEE36;CDG1S (epileptic encephalopathy, early infantile, 36), OMIM:300884)

Official abbreviation EIEE36;CDG1S
Name epileptic encephalopathy, early infantile, 36
OMIM ID 300884
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ALG13
Associated tissues -
Disease features -
Remarks -

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