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DO Term : developmental and epileptic encephalopathy 61 [DOID:0080434] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A developmental and epileptic encephalopathy that has_material_basis_in homozygous or compound heterozygous mutation in the ADAM22 gene on chromosome 7q21.

synonyms:
617933,
early infantile epileptic encephalopathy 61,
DEE61,
OMIM:617933

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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