GRIN2A developmental and epileptic encephalopathy

Glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A developmental and epileptic encephalopathy (disorder)

active

Code	`770431001`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20190131

Synonyms

Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
GRIN2A-DEE - GRIN2A developmental and epileptic encephalopathy
Glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A developmental and epileptic encephalopathy

Parents (6)

13028004Abnormal nervous system function finding
11164009Autosomal dominant hereditary disorder disorder
1275631007Developmental and epileptic encephalopathy disorder
363070008Developmental hereditary disorder disorder
1362108000Genetic intellectual disability disorder
363235000Hereditary disorder of nervous system disorder

Children (0)

None (leaf concept).