Disease #00168 (WMS; WS (Williams-Beuren syndrome), OMIM:194050)

Official abbreviation WMS; WS
Name Williams-Beuren syndrome
OMIM ID 194050
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene NCF1
Associated tissues -
Disease features -
Remarks -

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