Disease #06818 (DEE58 (encephalopathy, developmental and epileptic, type 58), OMIM:617830)

Official abbreviation DEE58
Name encephalopathy, developmental and epileptic, type 58
OMIM ID 617830
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 NTRK2
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited 2023-10-23 11:52:50 +02:00 (CEST)


Individuals

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00434154 253946 - - F no Portugal - - - - - DEE58 Neonatal hypotonia, Global developmental delay NTRK2 NTRK2 1 1 Andreas Laner
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