Term Name: developmental and epileptic encephalopathy 86
Synonyms: DEE86, early infantile epileptic encephalopathy 86
Definition: A developmental and epileptic encephalopathy that has_material_basis_in homozygous or compound heterozygous mutation in the DALRD2 gene on chromosome 3p21.31.
Ontology: Human Disease [DOID:0112220]   ( DOID:0112220 )

Relationships
is a type of: autosomal recessive disease developmental and epileptic encephalopathy