Anasarca	Disorder characterized by edema	Disorder characterized by fever	Fever	Inflammatory disorder	Systemic disease	Thrombocytopenic disorder
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Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder)
	TAFRO syndrome
	TAFRO (thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly) syndrome Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome
	A rare systemic disease characterized by acute or subacute onset of thrombocytopenia, anasarca (edema, pleural effusion, ascites) and systemic inflammation (fever and/or elevated C-reactive protein). Minor diagnostic categories are Castleman disease-like features on lymph node biopsy, reticulin myelofibrosis and/or increased number of megakaryocytes in bone marrow, progressive renal insufficiency and mild organomegaly including hepatosplenomegaly and lymphadenopathy. Most patients show elevated levels of serum alkaline phosphatase while marked polyclonal hypergammopathy is rare.
	syndroom van trombocytopenie, anasarca, koorts, nierinsufficiëntie en organomegalie
	syndroom van trombopenie, gegeneraliseerd oedeem, febris, nierschade en visceromegalie TAFRO-syndroom syndroom van trombopenie, gegeneraliseerd oedeem, pyrexie, nierschade en splanchnomegalie

Id	1187615007
Status	Primitive

Associated morphology

Associated morphology

Inflammatory morphology

Has interpretation	Abnormal
Interprets	Hemostatic function

Has interpretation	Below reference range
Interprets	Platelet count

Has interpretation	Above reference range
Interprets	Body temperature

ICD-10 complex map reference set

Target	M35.8
Rule	TRUE
Advice	ALWAYS M35.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified