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 -
Date created 2023-06-16 11:10:28 +00:00 (UTC)
Date last edited N/A

  Powered by LOVD v.3.0 Build 30
LOVD software ©2004-2024 Leiden University Medical Center 		There are currently no updates.