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Items: 4

1.

Mediastinal yolk sac tumor

An extragonadal non-seminomatous malignant germ cell tumor that arises from the mediastinum. It is characterized by the presence of small pale cells with small amount of cytoplasm and round to oval nuclei with small nucleoli forming a variety of patterns, including microcystic, macrocystic, pseudopapillary, myxomatous, hepatoid, polyvesicular vitelline, and solid. It manifests with respiratory distress, thoracic pain, fever, and superior vena cava syndrome. [from NCI]

MedGen UID:
233176
Concept ID:
C1334683
Neoplastic Process
2.

Iron metabolism disease

Disorders in the processing of iron in the body: its absorption, transport, storage, and utilization. [from MONDO]

MedGen UID:
8438
Concept ID:
C0012715
Disease or Syndrome
3.

Disorder of iron metabolism and transport

MedGen UID:
1826109
Concept ID:
C5681031
Disease or Syndrome
4.

Deficiency of isobutyryl-CoA dehydrogenase

Isobutyryl-CoA dehydrogenase (IBD) deficiency is a condition that disrupts the breakdown of certain proteins. Normally, proteins from food are broken down into parts called amino acids. Amino acids can be further processed to provide energy for growth and development. People with IBD deficiency have inadequate levels of an enzyme that helps break down a particular amino acid called valine.

Most people with IBD deficiency are asymptomatic, which means they do not have any signs or symptoms of the condition. A few children with IBD deficiency have developed features such as a weakened and enlarged heart (dilated cardiomyopathy), weak muscle tone (hypotonia), and developmental delay. This condition may also cause low numbers of red blood cells (anemia) and very low blood levels of carnitine, which is a natural substance that helps convert certain foods into energy. The range of signs and symptoms associated with IBD deficiency remains unclear because very few affected individuals have been reported. [from MedlinePlus Genetics]

MedGen UID:
370754
Concept ID:
C1969809
Disease or Syndrome
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