Disease #06389 (MRD62 (Intellectual developmental disorder 62), OMIM:618793)

Official abbreviation MRD62
Name Intellectual developmental disorder 62
OMIM ID 618793
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene DLG4
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00412301 199634 - - M - Germany - - - - - MRD62 Intellectual disability, moderate DLG4 DLG4 1 1 Andreas Laner
00427820 163126 - - M no Germany - - - - - MRD62 Global developmental delay, Flat midface, Deep set ears rotated backwards, Prominent incisors DLG4 DLG4 1 1 Andreas Laner
00436674 269120 - - M ? ? (unknown) - - - - - MRD62 Neurodevelopmental abnormality, Intellectual disability DLG4 DLG4 1 1 Andreas Laner
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