Disease #03968 (MRT37 (mental retardation, autosomal recessive, type 37 (MRT-37)), OMIM:615493)

Official abbreviation MRT37
Name mental retardation, autosomal recessive, type 37 (MRT-37)
OMIM ID 615493
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene ANK3
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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00434642 119324 - - M yes Turkey - - - - - MRT37 Microcephaly, Inappropriate laughter, Cerebellar hypoplasia, Myoclonus, Absent speech, Limb ataxia, Short stature, Neurodevelopmental delay,Serrated incisors ANK3 ANK3 1 1 Andreas Laner
00434904 119324 - - M yes Turkey - - - - - MRT37, NEDMHM Microcephaly, Inappropriate laughter, Cerebellar hypoplasia,(+) Myoclonus, Absent speech, Limb ataxia, Short stature, Neurodevelopmental delay, Serrated incisors ANK3, ARHGEF2 ANK3, ARHGEF2 2 1 Andreas Laner
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