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Results: 1 to 20 of 34

1.

Abnormal liver function

A finding that indicates abnormal liver function. [from NCI]

MedGen UID:
39248
Concept ID:
C0086565
Pathologic Function
2.

Choline

a organic chemical substance found in plants and animal organs [from CHV]

MedGen UID:
3048
Concept ID:
C0008405
Pharmacologic Substance
3.

Choline deficiency

A condition produced by a deficiency of CHOLINE in animals. Choline is known as a lipotropic agent because it has been shown to promote the transport of excess fat from the liver under certain conditions in laboratory animals. Combined deficiency of choline (included in the B vitamin complex) and all other methyl group donors causes liver cirrhosis in some animals. Unlike compounds normally considered as vitamins, choline does not serve as a cofactor in enzymatic reactions. (From Saunders Dictionary & Encyclopedia of Laboratory Medicine and Technology, 1984) [from MeSH]

MedGen UID:
930
Concept ID:
C0008412
Disease or Syndrome
4.

Decreased liver function

Reduced ability of the liver to perform its functions. [from HPO]

MedGen UID:
504835
Concept ID:
CN001291
Finding
5.

Functional disorder

Deranged function in an individual or an organ that is due to a disease. (MedicineNet.com) [from NCI]

MedGen UID:
124450
Concept ID:
C0277785
Pathologic Function
6.

Estrogens

A class of natural or synthetic hormones that binds to a cytoplasmic receptor and initiates translocation of the hormone-receptor complex to the nucleus of target cells of tissues rich in estrogen receptors, including the endometrium, myometrium, oviduct, vagina, fallopian tube, cervix, brain, liver, placenta, ovarian cells, Leydigs cells, kidney, prostate, pancreas, heart, and skin. (NCI) [from NCI]

MedGen UID:
8701
Concept ID:
C0014939
Pharmacologic Substance
7.

phosphatidylethanolamine

A phospholipid with the polar ethanolamine found in phosphoester linkage to diacylglycerol. [from NCI]

MedGen UID:
260779
Concept ID:
C1450468
Pharmacologic Substance
8.

Syndrome

A set of symptoms or conditions that occur together and suggest the presence of a certain disease or an increased chance of developing the disease. [from NCI]

MedGen UID:
11688
Concept ID:
C0039082
Disease or Syndrome
9.

Hepatic steatosis

The presence of `steatosis` (MPATH:622) in the `liver` (FMA:7197). [from HPO]

MedGen UID:
427871
Concept ID:
CN001278
Finding
10.

Disease Response

The pathologic and/or clinical changes that result from treatment. The changes may include eradication of detectable disease, stabilization of disease, or disease progression. [from NCI]

MedGen UID:
309976
Concept ID:
C1704632
Finding
11.

Receptor Binding

Receptor Binding involves a temporary non-covalent, typically highly specific and high affinity, interaction through intermolecular physical forces of attraction and spatial complementarity with a diverse group of intrinsic membrane or cytoplasmic proteins that mediate the biological effects of secreted regulatory signaling molecules through modification of the activity of signal transduction pathways. [from NCI]

MedGen UID:
154572
Concept ID:
C0597358
Molecular Function
12.

Triglyceride storage disease with ichthyosis

Chanarin-Dorfman syndrome is a condition in which fats (lipids) are stored abnormally in the body. Affected individuals cannot break down certain fats called triglycerides, and these fats accumulate in organs and tissues, including skin, liver, muscles, intestine, eyes, and ears. People with this condition also have dry, scaly skin (ichthyosis), which is usually present at birth. Additional features of this condition include an enlarged liver (hepatomegaly), clouding of the lens of the eyes (cataracts), difficulty with coordinating movements (ataxia), hearing loss, short stature, muscle weakness (myopathy), involuntary movement of the eyes (nystagmus), and mild intellectual disability. The signs and symptoms vary greatly among individuals with Chanarin-Dorfman syndrome. Some people may have ichthyosis only, while others may have problems affecting many areas of the body. [from GHR]

MedGen UID:
82780
Concept ID:
C0268238
Disease or Syndrome
13.

Fatty degeneration

A morphologic finding indicating intracytoplasmic fat accumulation in the liver parenchyma. [from NCI]

MedGen UID:
57759
Concept ID:
C0152254
Pathologic Function
14.

Vitamin deficiency

A disorder that is caused by the deficiency of a vitamin. The deficiency may result from either suboptimal vitamin intake or conditions that prevent the vitamin's use or absorption in the body. Representative examples include beriberi caused by thiamine deficiency, scurvy caused by vitamin C deficiency, and rickets caused by vitamin D deficiency. [from NCI]

MedGen UID:
267607
Concept ID:
C1510471
Disease or Syndrome
15.

Disease Attributes

Clinical characteristics of disease or illness. [from MeSH]

MedGen UID:
199876
Concept ID:
C0752357
Disease or Syndrome
16.

Avitaminosis

a disease due to a lack of a vitamin in the body [from CHV]

MedGen UID:
91216
Concept ID:
C0376286
Disease or Syndrome
17.

Malnutrition

Food provides the energy and nutrients you need to be healthy. If you don't get enough nutrients -- including proteins, carbohydrates, fats, vitamins, and minerals - you may suffer from malnutrition. Causes of malnutrition include:: -Lack of specific nutrients in your diet. Even the lack of one vitamin can lead to malnutrition. -An unbalanced diet. -Certain medical problems, such as malabsorption syndromes and cancers. Symptoms may include fatigue, dizziness and weight loss, or you may have no symptoms. Your doctor will do tests, depending on the cause of your problem. Treatment may include replacing the missing nutrients and treating the underlying cause.  [from MedlinePlus]

MedGen UID:
56429
Concept ID:
C0162429
Disease or Syndrome
18.

Nutritional and Metabolic Diseases

A collective term for nutritional disorders resulting from poor absorption or nutritional imbalance, and metabolic disorders resulting from defects in biosynthesis (ANABOLISM) or breakdown (CATABOLISM) of endogenous substances. [from MeSH]

MedGen UID:
45164
Concept ID:
C0028715
Disease or Syndrome
19.

Nutrition Disorders

MedGen UID:
45163
Concept ID:
C0028709
Disease or Syndrome
20.

Vitamin B Deficiency

A condition due to deficiency in any member of the VITAMIN B COMPLEX. These B vitamins are water-soluble and must be obtained from the diet because they are easily lost in the urine. Unlike the lipid-soluble vitamins, they cannot be stored in the body fat. [from MeSH]

MedGen UID:
22669
Concept ID:
C0042850
Disease or Syndrome

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