Disease #06018 (NEDMHM (?Neurodevelopmental disorder with midbrain and hindbrain malformations), OMIM:617523)

Official abbreviation NEDMHM
Name ?Neurodevelopmental disorder with midbrain and hindbrain malformations
OMIM ID 617523
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene ARHGEF2
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

1 entry on 1 page. Showing entry 1.
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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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