Disease #00141 (MWS (MUCKLE-WELLS SYNDROME), OMIM:191900)

Official abbreviation MWS
Name MUCKLE-WELLS SYNDROME
OMIM ID 191900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene NLRP3
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-16 11:12:22 +00:00 (UTC)
Date last edited N/A

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