Disease #05902 (MRD55 (mental retardation, autosomal dominant, type 55, with seizures), OMIM:617831)

Official abbreviation MRD55
Name mental retardation, autosomal dominant, type 55, with seizures
OMIM ID 617831
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 NUS1
Associated tissues -
Disease features -
Remarks -
Date created 2021-03-03 09:31:02 +01:00 (CET)
Date last edited 2023-10-23 15:21:12 +02:00 (CEST)


Individuals

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00380219 182970 - - M no Germany - - - - - MRD55 Ataxia, Muscle weakness, Tremor, Involuntary movements, Abnormality of coordination, Abnormal muscle physiology NUS1 NUS1 1 1 Andreas Laner
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