Autosomal recessive hereditary disorder	Complement component 3 glomerulopathy	Hereditary nephritis	Mesangiocapillary glomerulonephritis
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Dense deposit disease (disorder)
	Dense deposit disease
	MCGN type II - mesangiocapillary glomerulonephritis type II Membranoproliferative glomerulonephritis type 2 MPGNII - membranoproliferative glomerulonephritis type II Mesangiocapillary glomerulonephritis type 2
	A histological subtype of C3 glomerulopathy with characteristics of C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.
	dense deposit disease
	DDD

Id	722760002
Status	Primitive

Clinical course

Associated morphology	Chronic proliferative inflammation
Finding site	Structure of glomerular mesangium

PALGA thesaurus simple reference set for pathology

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	N03.6
Rule	TRUE
Advice	ALWAYS N03.6 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION \| POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE
Correlation	SNOMED CT source code to target map code correlation not specified

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Persistent hematuria co-occurrent and due to dense deposit disease

Recurrent hematuria co-occurrent and due to dense deposit disease