Term Name: developmental and epileptic encephalopathy 109
Synonyms: DEE109
Definition: A developmental and epileptic encephalopathy characterized by onset of various types of seizures in the first months or years of life that has_material_basis_in heterozygous mutation in the FZR1 gene on chromosome 19p13.
Ontology: Human Disease [DOID:0070378]   ( DOID:0070378 )

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