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Etymologie

Was (wer) ist cytomegalic inclusion disease virus - definition

HUMAN DISEASE

Mucolipidosis II; Inclusion-cell disease; Inclusion cell disease; Inclusion-Cell Disease; Mucolipidosis Ii; ML II; I cell disease; I Cell disease; I Cell Disease

Cytomegalic inclusion body disease

MEDICAL CONDITION

Cytomegalic inclusion body disease (CIBD) also known as cytomegalic inclusion disease (CID) is a series of signs and symptoms caused by cytomegalovirus infection, toxoplasmosis or other rare infections such as herpes or rubella viruses. It can produce massive calcification of the central nervous system, and often the kidneys.

https://en.wikipedia.org/wiki/Cytomegalic_inclusion_body_disease

Infectious bursal disease

SPECIES OF VIRUS

IBDV; Infectious Bursal Disease virus; Ibdv; Infectious bursal disease virus; Infectious Bursal Disease; Gumboro disease

Infectious bursal disease (IBD), also known as Gumboro disease, infectious bursitis and infectious avian nephrosis, is a highly contagious disease of young chickens and turkeys caused by infectious bursal disease virus (IBDV), characterized by immunosuppression and mortality generally at 3 to 6 weeks of age. The disease was first discovered in Gumboro, Delaware in 1962.

https://en.wikipedia.org/wiki/Infectious_bursal_disease

Pepper mild tigré virus

MEMBER VIRUS OF BEGOMOVIRUS

Pepper mild tigre virus; Tigre disease virus

Pepper mild tigré virus (PepMTV) is a plant pathogenic virus of the family Geminiviridae. It was demoted from species status in 2002.

https://en.wikipedia.org/wiki/Pepper_mild_tigré_virus

Wikipedia

I-cell disease

Inclusion-cell (I-cell) disease, also referred to as mucolipidosis II (ML II), is part of the lysosomal storage disease family and results from a defective phosphotransferase (an enzyme of the Golgi apparatus). This enzyme transfers phosphate to mannose residues on specific proteins. Mannose-6-phosphate serves as a marker for proteins to be targeted to lysosomes within the cell. Without this marker, proteins are instead secreted outside the cell, which is the default pathway for proteins moving through the Golgi apparatus. Lysosomes cannot function without these proteins, which function as catabolic enzymes for the normal breakdown of substances (e.g. oligosaccharides, lipids, and glycosaminoglycans) in various tissues throughout the body (i.e. fibroblasts). As a result, a buildup of these substances occurs within lysosomes because they cannot be degraded, resulting in the characteristic I-cells, or "inclusion cells" seen microscopically. In addition, the defective lysosomal enzymes normally found only within lysosomes are instead found in high concentrations in the blood, but they remain inactive at blood pH (around 7.4) because they require the low lysosomal pH 5 to function.

https://en.wikipedia.org/wiki/I-cell disease