Human genes for CINCA Syndrome
CINCA Syndrome [DOID:0090029]
An autoimmune disease characterized by neonatal onset of cutaneous symptoms, chronic meningitis, and joint manifestations with recurrent fever and inflammation that has_material_basis_in heterozygous mutation in the NLRP3 gene on chromosome 1q.
Synonyms: CINCA Syndrome, CINCA disease, CINCA disorder, CINCA Syndromes, DOID:0090029 ...