Disease #00807 (MRD6 (mental retardation, autosomal dominant, type 6), OMIM:613970)

Official abbreviation MRD6
Name mental retardation, autosomal dominant, type 6
OMIM ID 613970
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 GRIN2B
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-02-01 18:27:16 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00080992 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - MRD6 Mental retardation, autosomal dominant 6 (OMIM:613970) GRIN2B GRIN2B 1 1 Daniel Trujillano
00080998 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - MRD6 Mental retardation, autosomal dominant 6 (OMIM:613970) GRIN2B GRIN2B 1 1 Daniel Trujillano
00435125 65503 - - M no Germany - - - - - MRD6 Global developmental delay, Autistic behavior, Attention deficit hyperactivity disorder, Intellectual disability, Myopia, Scoliosis, Hemihypertrophy of lower limb, Decreased body weight GRIN2B GRIN2B 1 1 Andreas Laner
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