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Hereditary periodic fever syndrome

MONDO:0017953

An instance of periodic fever syndrome that is caused by an inherited modification of the individual's genome.

Also known as: hereditary periodic fever syndrome

33 clinical trials for this condition and its sub-types.

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Sub-types

Familial Mediterranean fever (14) Cryopyrin-associated periodic syndrome (10) CINCA syndrome (4) TNF receptor 1-associated periodic fever syndrome (4) Familial cold autoinflammatory syndrome (3) Mevalonate kinase deficiency (3) Muckle-Wells syndrome (3) Hyperimmunoglobulinemia D with periodic fever (2) Periodic fever-infantile enterocolitis-autoinflammatory syndrome (2) Autoinflammation, panniculitis, and dermatosis syndrome, autosomal recessive (0) Autosomal recessive familial Mediterranean fever (0) Familial cold autoinflammatory syndrome 1 (0) Familial cold autoinflammatory syndrome 2 (0) Familial cold autoinflammatory syndrome 3 (0) Familial cold autoinflammatory syndrome 4 (0) Familial Mediterranean fever, autosomal dominant (0) Mevalonic aciduria (0)

Broader categories

Disease (680) Hereditary disease (176) Rheumatic disorder (87) Connective tissue disorder (68) Syndromic disease (25) Autoinflammatory syndrome (21) Human disease (14) Disease of genetic or genomic mechanism (2) Periodic fever syndrome (2) Disease by body system or component (0)

Trials to join now! 17 Not yet recruiting 7 Not yet finished but already full! 3 Completed 6