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Results: 8

1.

Recurrence (disease attribute)

The return of a sign, symptom, or disease after a remission. [from MeSH]

MedGen UID:
416712
Concept ID:
C2825055
Pathologic Function
2.

Glomerulonephritis

A renal disorder characterized by damage in the glomeruli. It may be acute or chronic, focal or diffuse, and it may lead to renal failure. Causes include autoimmune disorders, infections, diabetes, and malignancies. [from NCI]

MedGen UID:
6616
Concept ID:
C0017658
Disease or Syndrome
3.

Dense deposit disease

A type of membranoproliferative glomerulonephritis characterized by electron dense deposits at the glomerular basement membrane. [from HPO]

MedGen UID:
505672
Concept ID:
CN004197
Finding
4.

Membranoproliferative glomerulonephritis

Proliferation of mesangial cells, increase in the mesangial extracellular matrix, and a thickening of the glomerular capillary walls. [from HPO]

MedGen UID:
504601
Concept ID:
CN000741
Finding
5.

Glomerulonephritis

Inflammation of the renal glomeruli. [from HPO]

MedGen UID:
504340
Concept ID:
CN000099
Finding
6.

Spondylometaepiphyseal dysplasia short limb-hand type

MedGen UID:
338595
Concept ID:
C1849011
Disease or Syndrome
7.

Mesangiocapillary glomerulonephritis, type II

Dense deposit disease (DDD)/membranoproliferative glomerulonephritis type II (MPGNII) is characterized by onset of hematuria and/or proteinuria, acute nephritic syndrome, or nephrotic syndrome. It most frequently affects children between ages five and 15 years. Spontaneous remissions are uncommon and about 50% of affected individuals develop end-stage renal disease (ESRD) within ten years of diagnosis. DDD/MPGNII can be associated with acquired partial lipodystrophy (APL). Drusen, whitish-yellow deposits within Bruch's membrane of the retina often develop in the second decade of life; they initially have little impact on vision, but cause vision problems from subretinal neovascular membranes, macular detachment, and central serous retinopathy in about 10% of affected individuals. [from GeneReviews]

MedGen UID:
124345
Concept ID:
C0268743
Disease or Syndrome
8.

Mesangiocapillary glomerulonephritis

Chronic glomerulonephritis characterized histologically by proliferation of MESANGIAL CELLS, increase in the MESANGIAL EXTRACELLULAR MATRIX, and a thickening of the glomerular capillary walls. This may appear as a primary disorder or secondary to other diseases including infections and autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Various subtypes are classified by their abnormal ultrastructures and immune deposits. Hypocomplementemia is a characteristic feature of all types of MPGN. [from MeSH]

MedGen UID:
9033
Concept ID:
C0017662
Disease or Syndrome

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