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Items: 4

1.

Pain

MedGen UID:
880950
Concept ID:
CN236637
Disease or Syndrome
2.

Pain

MedGen UID:
776584
Concept ID:
C2364139
Finding
3.

Histiocytoma

A neoplasm containing histiocytes. [from HPO]

MedGen UID:
507025
Concept ID:
CN178692
Finding
4.

Benign familial hematuria

Benign familial hematuria is an autosomal dominant condition manifest as nonprogressive isolated microscopic hematuria that does not result in renal failure. It is characterized pathologically by thinning of the glomerular basement membrane (GBM), and can be considered the mildest end of the spectrum of renal diseases due to type IV collagen defects of the basement membrane. The most severe end of the spectrum is represented by Alport syndrome (301050; 203780, 104200), which results in end-stage renal failure and may be associated with hearing loss and ocular anomalies (review by Lemmink et al. (1996)). [from OMIM]

MedGen UID:
66039
Concept ID:
C0241908
Disease or Syndrome
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