Autosomal dominant hereditary disorder	Hereditary disorder of immune system	Hereditary periodic fever
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NLR family pyrin domain containing 12-associated hereditary periodic fever syndrome (disorder)
	NLRP12-associated hereditary periodic fever syndrome
	FCAS2 - familial cold autoinflammatory syndrome type 2 NLR family pyrin domain containing 12-associated hereditary periodic fever syndrome Familial cold autoinflammatory syndrome type 2
	A rare autoinflammatory syndrome with characteristics of episodic and recurrent periods of fever combined with various systemic manifestations such as myalgia, arthralgia, joint swelling, urticaria, headache and skin rash. Common trigger of these episodes is cold. There is evidence the disease is caused by heterozygous mutation in the NLRP12 gene on chromosome 19q13.
	NLRP12-geassocieerd hereditair periodiekekoortssyndroom
	familiair koudegeïnduceerd auto-inflammatoir syndroom type 2 NLRP12-geassocieerde periodieke koorts FCAS2 'familial cold autoinflammatory syndrome' type 2

Id	783146009
Status	Primitive

Associated morphology	Inflammatory morphology
Finding site	Structure of immune system
Pathological process	Abnormal immune process

Clinical course

Has interpretation	Above reference range
Interprets	Body temperature

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E85.0
Rule	TRUE
Advice	ALWAYS E85.0 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified