Disease #05621 (MKHK1 (Menke-Hennekam syndrome, type 1 (MKHK-1)), OMIM:618332)

Official abbreviation MKHK1
Name Menke-Hennekam syndrome, type 1 (MKHK-1)
OMIM ID 618332
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene CREBBP
Associated tissues -
Disease features -
Remarks -
Date created 2019-07-05 14:50:59 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00397652 189764 - - M no Germany - - - - - MKHK1 Mild global developmental delay, Specific learning disability, Protruding ea CREBBP CREBBP 1 1 Andreas Laner
00431863 213718 - - M no Germany - - - - - MKHK1 Delayed speech and language development, Global developmental delay, Motor delay, Delayed social development, Hypotonia CREBBP CREBBP 1 1 Andreas Laner
00433676 - - - M - - - - - - - MKHK1 autism, hyperactivity, motor delay, aggressive behaviour, facial abnormality - CREBBP 1 1 Marketa Wayhelova
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