Disease-gene associations mined from literature

Human genes for CINCA Syndrome

CINCA Syndrome [DOID:0090029]

An autoimmune hypersensitivity 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 ...