Disease #05531 (CLABARS;MRD49 (Clark-Baraitser syndrome (CLABARS, MRD-49)), OMIM:617752)

Official abbreviation CLABARS;MRD49
Name Clark-Baraitser syndrome (CLABARS, MRD-49)
OMIM ID 617752
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene TRIP12
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2018-12-18 09:17:05 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00390483 187344 - - M no Germany - - - - - CLABARS;MRD49 Hydrocele testis, Behavioral abnormality, Delayed speech and language development, Global developmental delay TRIP12 TRIP12 1 1 Andreas Laner
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