Disease #01609 (Williams syndrome, OMIM:194050)

Official abbreviation -
Name Williams syndrome
OMIM ID 194050
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes ELN, MLXIPL
Associated tissues -
Disease features -
Remarks -