Disease #01594 (MWS (Muckle-Wells syndrome (MWS)), OMIM:191900)
Official abbreviation |
MWS |
Name |
Muckle-Wells syndrome (MWS) |
OMIM ID |
191900 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
14 |
Phenotype entries for this disease |
14 |
Associated with 1 gene |
NLRP3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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