Cryopyrin-Associated Periodic Syndromes

"Cryopyrin-Associated Periodic Syndromes" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

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A group of rare autosomal dominant diseases, commonly characterized by atypical URTICARIA (hives) with systemic symptoms that develop into end-organ damage. The atypical hives do not involve T-cell or autoantibody. Cryopyrin-associated periodic syndrome includes three previously distinct disorders: Familial cold autoinflammatory syndrome; Muckle-Wells Syndrome; and CINCA Syndrome, that are now considered to represent a disease continuum, all caused by NLRP3 protein mutations.

Descriptor ID	D056587
MeSH Number(s)	C16.320.382.500 C17.800.827.368.500
Concept/Terms	Cryopyrin-Associated Periodic Syndromes Cryopyrin-Associated Periodic Syndromes Cryopyrin Associated Periodic Syndromes Cryopyrin-Associated Periodic Syndrome Periodic Syndrome, Cryopyrin-Associated Periodic Syndromes, Cryopyrin-Associated Syndrome, Cryopyrin-Associated Periodic Syndromes, Cryopyrin-Associated Periodic Cryopyrinopathy Cryopyrinopathies Familial Cold Autoinflammatory Syndrome Familial Cold Autoinflammatory Syndrome Familial Cold Urticaria Cold Urticaria, Familial Cold Urticarias, Familial Familial Cold Urticarias Urticaria, Familial Cold Urticarias, Familial Cold Muckle-Wells Syndrome Muckle-Wells Syndrome Muckle Wells Syndrome Syndrome, Muckle-Wells Urticaria-Deafness-Amyloidosis Syndrome Syndrome, Urticaria-Deafness-Amyloidosis Syndromes, Urticaria-Deafness-Amyloidosis Urticaria Deafness Amyloidosis Syndrome Urticaria-Deafness-Amyloidosis Syndromes Urticaria, Deafness and Amyloidosis Chronic Infantile Neurological, Cutaneous, and Articular Syndrome Chronic Infantile Neurological, Cutaneous, and Articular Syndrome CINCA Syndrome NOMID IOMID IOMIDs Multisystem Inflammatory Disease, Neonatal-Onset Multisystem Inflammatory Disease, Neonatal Onset Neonatal Onset Multisystem Inflammatory Disease Chronic, Infantile, Neurological, Cutaneous, Articular Syndrome Infantile Onset Multisystem Inflammatory Disease

Below are MeSH descriptors whose meaning is more general than "Cryopyrin-Associated Periodic Syndromes".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Hereditary Autoinflammatory Diseases [C16.320.382]
Cryopyrin-Associated Periodic Syndromes [C16.320.382.500]
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Skin Diseases, Genetic [C17.800.827]
Hereditary Autoinflammatory Diseases [C17.800.827.368]
Cryopyrin-Associated Periodic Syndromes [C17.800.827.368.500]

Below are MeSH descriptors whose meaning is related to "Cryopyrin-Associated Periodic Syndromes".

Below are MeSH descriptors whose meaning is more specific than "Cryopyrin-Associated Periodic Syndromes".

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