Disease #00137 (CINCA (CINCA SYNDROM), OMIM:607115)

Official abbreviation CINCA
Name CINCA SYNDROM
OMIM ID 607115
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 -

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