Disease #07155 (MRD64 (intellectual developmental disorder, autosomal dominant, type 64), OMIM:619188)

Official abbreviation MRD64
Name intellectual developmental disorder, autosomal dominant, type 64
OMIM ID 619188
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 ZNF292
Associated tissues -
Disease features -
Remarks -
Date created 2025-03-06 14:07:33 +01:00 (CET)
Date last edited N/A


Individuals

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00472017 356839 - - M no Germany - - - - - MRD64 Neurodevelopmental delay, Intellectual disability, borderline, Attention deficit hyperactivity disorder, Atypical behavior, Tip-toe gait, EEG abnormality, Hypotonia, Smooth philtrum, Short nose ZNF292 ZNF292 1 1 Andreas Laner
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