Disease #03124 (MRD22;del1q43q44 (mental retardation, autosomal dominant, type 22 (MRD22, 1q43-q44 deletion syndrome)), OMIM:612337)

Official abbreviation MRD22;del1q43q44
Name mental retardation, autosomal dominant, type 22 (MRD22, 1q43-q44 deletion syndrome)
OMIM ID 612337
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 ZBTB18
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00385789 185943 - - M ? - - - - - - MRD22;del1q43q44 Intellectual disability, Hearing impairment, Seizure, Delayed speech and language development, Hypoplasia of the corpus callosum ZBTB18 ZBTB18 1 1 Andreas Laner
00435153 P1 - - F no Spain - - - - - MRD22;del1q43q44 - - ZBTB18 1 2 Alejandro Brea-Fernández
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