Disease #06372 (DEE72 (encephalopathy, developmental and epileptic, 72), OMIM:618374)

Official abbreviation DEE72
Name encephalopathy, developmental and epileptic, 72
OMIM ID 618374
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene NEUROD2
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited 2022-05-30 12:43:01 +02:00 (CEST)

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