Disease #06007 (MRD42 (Mental retardation, autosomal dominant 42), OMIM:616973)

Official abbreviation MRD42
Name Mental retardation, autosomal dominant 42
OMIM ID 616973
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene GNB1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00436387 268932 - - F no (Armenia) - - - - - MRD42 Neurodevelopmental delay, Motor delay - - - 1 Andreas Laner
00436388 268932 - - F no Armenia - - - - - MRD42 Neurodevelopmental delay, Motor delay GNB1 GNB1 1 1 Andreas Laner
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