Disease #01609 (WBS (Williams-Beuren syndrome), OMIM:194050)

Official abbreviation WBS
Name Williams-Beuren syndrome
OMIM ID 194050
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 2 genes ELN, MLXIPL
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-02-24 17:26:01 +01:00 (CET)


Individuals

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00472816 Fam3PatII4 PubMed: Murdock 2021 mother F - Canada - - - - - WBS see paper; ..., Williams syndrome; mild cognitive disability; leg cramping, difficulty walking upstairs, normal neuromuscular exam; no dilated cardiomyopathy; normal CK levele33–111 U/L >1200 U/L during episode of chest pain DMD DMD 1 1 Johan den Dunnen
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