Cinca Syndrome (CINCA)

Alias:

Neonatal-Onset Multisystem Inflammatory Disease

Infantile-Onset Multisystem Inflammatory Disease

Cryopyrin-Associated Periodic Syndrome 3

Prieur-Griscelli Syndrome

Iomid Syndrome

Nomid Syndrome

Cinca

Chronic Infantile Neurological, Cutaneous and Articular Syndrome

Chronic Infantile Neurological Cutaneous and Articular Syndrome

Chronic Neurologic Cutaneous and Articular Syndrome

Nomid

Caps3

Chronic Infantile Neurological, Cutaneous, and Articular Syndrome

Chronic, Infantile, Neurological, Cutaneous, Articular Syndrome

Chronic Infantile Neurologic Cutaneous and Articular Syndrome

Chronic Infantile Neurological Cutaneous Articular Syndrome

Multisystem Inflammatory Disease, Neonatal-Onset

Neonatal Onset Multisystem Inflammatory Disease

Cryopyrin-Associated Periodic Syndromes

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Cinca Syndrome, also known as neonatal-onset multisystem inflammatory disease, is related to cryopyrin-associated periodic syndrome and exanthem, and has symptoms including recurrent fevers An important gene associated with Cinca Syndrome is NLRP3 (NLR Family Pyrin Domain Containing 3), and among its related pathways/superpathways are Infectious disease and Innate Immune System. The drugs Ginseng and Calcium polycarbophil have been mentioned in the context of this disorder. Affiliated tissues include skin and spinal cord, and related phenotypes are nausea and vomiting and hearing impairment

Related ID：

MALACARDS：CNC002

OMIM：607115

MESH：D056587