Disease #05770 (KLEFS2 (Kleefstra syndrome, type 2 (KLEFS2)), OMIM:617768)

Official abbreviation KLEFS2
Name Kleefstra syndrome, type 2 (KLEFS2)
OMIM ID 617768
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 4
Associated with 1 gene MLL3
Associated tissues -
Disease features developmental delay, intellectual disability, behavioral and psychiatric problems, hypotonia, seizures, short stature
Remarks -
Date created 2020-06-12 11:39:49 +02:00 (CEST)
Date last edited 2024-08-15 19:32:11 +02:00 (CEST)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00391855 215P - - F no Spain - - - - - KLEFS2 - - MLL3 1 1 Alejandro Brea-Fernández
00398613 190753 - prenatal trio-exom analysis M no (Spain) - - - - - KLEFS2 Increased nuchal translucency (5,3 mm) - - - 1 Andreas Laner
00398614 190753 - prenatal trio-exom M no (Spain) - - - - - KLEFS2 Increased nuchal translucency (5,3 mm) MLL3 MLL3 1 1 Andreas Laner
00458528 313255 - - F ? Turkey - - - - - KLEFS2 Global developmental delay, Atypical behavior, Exodeviation, Aggressive behavior, Expressive language delay KMT2D - - 1 Andreas Laner
00458529 313255 - - F ? Turkey - - - - - KLEFS2 Global developmental delay, Atypical behavior, Exodeviation, Aggressive behavior, Expressive language delay MLL3 MLL3 1 1 Andreas Laner
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