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Items: 11

1.

breast cancer

MedGen UID:
880206
Concept ID:
CN235590
Finding
2.

Breast cancer

MedGen UID:
808165
Concept ID:
CN221572
Disease or Syndrome
3.

disease-free survival

MedGen UID:
776920
Concept ID:
CN186048
Finding
4.

Neoplasm of the breast

A tumor (abnormal growth of tissue) of the breast. [from HPO]

MedGen UID:
506444
Concept ID:
CN116912
Finding
5.

Breast carcinoma

The presence of a carcinoma of the breast. [from HPO]

MedGen UID:
428324
Concept ID:
CN002714
Finding
6.

Neoplasm of breast

Tumors or cancer of the human BREAST. [from MeSH]

MedGen UID:
264172
Concept ID:
C1458155
Neoplastic Process
7.

Fanconi renotubular syndrome 1

Fanconi renotubular syndrome is a consequence of decreased solute and water reabsorption in the proximal tubule of the kidney. Patients have polydipsia and polyuria with phosphaturia, glycosuria, and aminoaciduria. They may develop hypophosphatemic rickets or osteomalacia, acidosis, and a tendency toward dehydration. Some will eventually develop renal insufficiency. Common laboratory abnormalities include glucosuria with a normal serum glucose, hyperaminoaciduria, hypophosphatemia, progressive renal insufficiency, renal sodium and potassium wasting, acidosis, uricosuria, and low-molecular-weight proteinuria (summary by Lichter-Konecki et al., 2001). Genetic Heterogeneity of Fanconi Renotubular Syndrome Fanconi renotubular syndrome-1 has been mapped to chromosome 15q15.3. See also FRTS2 (613388), caused by mutation in the SLC34A1 gene (182309) on chromosome 5q35; FRTS3 (615605), caused by mutation in the EHHADH gene (607037) on chromosome 3q27; and FRTS4 (616026), which is associated with maturity-onset diabetes of the young (MODY), caused by mutation in the HNF4A gene (600281) on chromosome 20q13. [from OMIM]

MedGen UID:
137960
Concept ID:
C0341703
Disease or Syndrome
8.

Fanconi syndrome

A genetic or acquired disorder characterized by impairment of the function of the proximal tubules of the kidney. It results in decreased reabsorption of electrolytes, glucose, amino acids, and other nutrients. [from NCI]

MedGen UID:
4653
Concept ID:
C0015624
Disease or Syndrome
9.

Disorder due cytochrome p450 CYP3A4

MedGen UID:
760103
Concept ID:
CN181501
Sign or Symptom
10.

Disorder due cytochrome p450 CYP3A5 variant

MedGen UID:
760102
Concept ID:
CN181500
Sign or Symptom
11.

Disorder due cytochrome p450 CYP2D6 variant

MedGen UID:
449534
Concept ID:
C1827409
Disease or Syndrome
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