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DO Term : CINCA Syndrome [DOID:0090029] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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:
  • NOMID syndrome,
  • OMIM:607115,
  • IOMID syndrome,
  • 607115,
  • Prieur-Griscelli syndrome,
  • chronic neurologic cutaneous and articular syndrome,
  • neonatal-onset multisystem inflammatory disease,
  • infantile-onset multisystem inflammatory disease,
  • cryopyrin-associated periodic syndrome 3,
  • ORDO:1451,
  • ICD10CM:E85.0,
  • chronic infantile neurological cutaneous articular syndrome
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Disease

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Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents