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Items: 20

1.

Familial Amyloidosis

An autosomal dominant inherited form of amyloidosis. [from NCI]

MedGen UID:
148146
Concept ID:
C0740340
Disease or Syndrome
2.

Amyloidosis

A disorder characterized by the localized or diffuse accumulation of amyloid protein in various anatomic sites. It may be primary, due to clonal plasma cell proliferations; secondary, due to long standing infections, chronic inflammatory disorders, or malignancies; or familial. It may affect the nerves, skin, tongue, joints, heart, liver, spleen, kidneys and adrenal glands. [from NCI]

MedGen UID:
272
Concept ID:
C0002726
Disease or Syndrome
3.

Renal amyloidosis

A form of amyloidosis that affects the kidney. [from HPO]

MedGen UID:
120633
Concept ID:
C0268382
Disease or Syndrome
4.

Progressive hereditary glomerulonephritis without deafness

MedGen UID:
98012
Concept ID:
C0403443
Disease or Syndrome
5.

Familial visceral amyloidosis, Ostertag type

MedGen UID:
82799
Concept ID:
C0268389
Disease or Syndrome
6.

Hereditary amyloidosis

Diseases in which there is an inherited mutation leading to AMYLOIDOSIS. [from MeSH]

MedGen UID:
64541
Concept ID:
C0206246
Disease or Syndrome
7.

Nephrotic syndrome

A collection of symptoms that include severe edema, proteinuria, and hypoalbuminemia; it is indicative of renal dysfunction. [from NCI]

MedGen UID:
10308
Concept ID:
C0027726
Disease or Syndrome
8.

Hypertension

Blood pressure that is abnormally high. [from NCI]

MedGen UID:
6969
Concept ID:
C0020538
Disease or Syndrome
9.

Hereditary amyloidosis

MedGen UID:
891681
Concept ID:
CN237687
Finding
10.

Hypertension

A finding of increased blood pressure; not necessarily hypertensive disorder [from SNOMEDCT_US]

MedGen UID:
635666
Concept ID:
C0497247
Finding
11.

Nephrotic syndrome

Nephrotic syndrome is a collection of findings resulting from glomerular dysfunction with an increase in glomerular capillary wall permeability associated with pronounced proteinuria. Nephrotic syndrome refers to the constellation of clinical findings that result from severe renal loss of protein, with Proteinuria and hypoalbuminemia, edema, and hyperlipidemia. [from HPO]

MedGen UID:
504341
Concept ID:
CN000100
Finding
12.

Maternal

A designation that has some relationship to motherhood. [from NCI]

MedGen UID:
348949
Concept ID:
C1858460
Finding
13.

Proteostasis Deficiencies

Disorders caused by imbalances in the protein homeostasis network - synthesis, folding, and transport of proteins; post-translational modifications; and degradation or clearance of misfolded proteins. [from MeSH]

MedGen UID:
403490
Concept ID:
C2718000
Cell or Molecular Dysfunction
14.

Male Urogenital Diseases

Pathological processes of the male URINARY TRACT and the reproductive system (GENITALIA, MALE). [from MeSH]

MedGen UID:
318601
Concept ID:
C1720894
Disease or Syndrome
15.

Female Urogenital Diseases

Pathological processes of the female URINARY TRACT and the reproductive system (GENITALIA, FEMALE). [from MeSH]

MedGen UID:
318599
Concept ID:
C1720887
Disease or Syndrome
16.

Disorder of urinary tract

Disorders of any part of the urologic system. [from NCI]

MedGen UID:
21791
Concept ID:
C0042075
Disease or Syndrome
17.

Nephropathy

A nonspecific term referring to disease or damage of the kidneys. [from HPO]

MedGen UID:
9635
Concept ID:
C0022658
Disease or Syndrome
18.

Imidazole

MedGen UID:
7016
Concept ID:
C0020923
Organic Chemical; Pharmacologic Substance
19.

Imidazoles

Compounds containing 1,3-diazole, a five membered aromatic ring containing two nitrogen atoms separated by one of the carbons. Chemically reduced ones include IMIDAZOLINES and IMIDAZOLIDINES. Distinguish from 1,2-diazole (PYRAZOLES). [from MeSH]

MedGen UID:
5743
Concept ID:
C0020924
Organic Chemical; Pharmacologic Substance
20.

Electrocardiograms

MedGen UID:
3992
Concept ID:
C0013798
Finding
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