Disease #04655 (MRD29 (mental retardation, autosomal dominant, type 29 (MRD29)), OMIM:616078)

Official abbreviation MRD29
Name mental retardation, autosomal dominant, type 29 (MRD29)
OMIM ID 616078
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 6
Phenotype entries for this disease 3
Associated with 1 gene SETBP1
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2020-11-03 13:29:43 +01:00 (CET)


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00315900 MR3016_01 - - M no Italy - - - - - MRD29 - - SETBP1 1 1 Emanuela Leonardi
00315901 MR2274_01 - - M no Italy - - - - - MRD29 - - SETBP1 1 1 Emanuela Leonardi
00391858 241P - - F no Spain - - - - - ID, MRD29, SGS - - SETBP1 1 1 Alejandro Brea-Fernández
00401306 083P - - M no Spain - - - - - ID, MRD29, SGS - - SETBP1 1 1 Alejandro Brea-Fernández
00428281 211479 - - F no Germany - - - - - MRD29 Macrocephaly, Mild global developmental delay, Infantile axial hypotonia, Motor delay, High palate; mother reported to have macrocephaly as well SETBP1 SETBP1 1 1 Andreas Laner
00464360 - - - - - - - - - - - MRD29 - SETBP1 SETBP1 1 1 Min Peng
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