Disease #04458 (DEE33 (encephalopathy, developmental and epileptic, type 33), OMIM:616409)

Official abbreviation DEE33
Name encephalopathy, developmental and epileptic, type 33
OMIM ID 616409
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene EEF1A2
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2024-02-02 17:33:40 +01:00 (CET)


Individuals

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00239789 XYHF4P1 - - M no China - 03y - - - DEE33 - EEF1A2 EEF1A2 1 1 Yin Xiaomeng
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