developmental and epileptic encephalopathy 61

Summary

DOID:0080434 - developmental and epileptic encephalopathy 61

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

Synonyms: DEE61, early infantile epileptic encephalopathy 61

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: adam22

MIM:

MIM:617933 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 61; DEE61

MIM:617933 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 61; DEE61

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), developmental and epileptic encephalopathy (is_a)