Disease #06941 (MRD67 (intellectual developmental disorder, autosomal dominant, type 67), OMIM:619927)

Official abbreviation MRD67
Name intellectual developmental disorder, autosomal dominant, type 67
OMIM ID 619927
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 GRIA1
Associated tissues -
Disease features -
Remarks -
Date created 2022-06-30 19:41:11 +02:00 (CEST)
Date last edited N/A


Individuals

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00466206 334573 - - M - Germany - - - - - MRD67 Intellectual disability, mild, Attention deficit hyperactivity disorder GRIA1 GRIA1 1 1 Andreas Laner
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