Disease #06355 (MRD61 (Intellectual developmental disorder 61), OMIM:618009)

Official abbreviation MRD61
Name Intellectual developmental disorder 61
OMIM ID 618009
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene MED13
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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00401305 068P - - M no Spain - - - - - MRD61 - - MED13 1 1 Alejandro Brea-Fernández
00435238 245434 - - F no Germany - - - - - MRD61 Cognitive impairment, Neurodevelopmental delay, Difficulty climbing stairs MED13 MED13 1 1 Andreas Laner
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