| XDP | xanthine diphosphate; xeroderma pigmentosum |
|---|---|
| XP | xanthogranulomatous pyelonephritis; xeroderma pigmentosum |
| XPA | xeroderma pigmentosum group A |
| XPC | xeroderma pigmentosum group C |
| XTE | xeroderma, talipes, and enamel defect [syndrome] |
| XP | Xeroderma Pigmentosum |
|---|---|
| XP-A | Xeroderma Pigmentosum complementation group A |
| XPA | Xeroderma pigmentosum group A |
| XP-V | Xeroderma pigmentosum variant |
| XP-C | xeroderma pigmentosum complementation group C |
| xeroderma pigmentosum | <disease> A rare inherited (autosomal recessive) disease in humans associated with increased sensitivity to ultraviolet induced mutagenesis and thus skin cancer. Sensitivity can be demonstrated in cultured cells and appears to be due to deficiency in DNA repair, specifically in excision of ultraviolet induced thymine dimers. Afflicted individuals are extremely sensitive to light and develop eye and skin abnormalities such as premature aging, keratoses and skin cancers and must be kept completely away from UV light. Inheritance: autosomal recessive. (18 Nov 1997) |
|---|
| xeroderma | <medicine> Ichthyosis. A skin disease characterised by the presence of numerous small pigmented spots resembling freckles, with which are subsequently mingled spots of atrophied skin. Origin: NL, fr. Gr. Dry + skin. Source: Websters Dictionary (01 Mar 1998) |
|---|
Synonyms : Kaposi's Disease, Kaposis Disease
Synonyms : XPA Nucleotide Excision Repair Protein, XPA Repair Protein, Xeroderma Pigmentosum Group A Complementing Protein, Xeroderma Pigmentosum-A Protein, Xeroderma Pigmentosum A Protein
Synonyms : ERCC2 Protein, Excision Repair Cross-Complementing Rodent Repair Deficiency, Group 2 Protein, Xeroderma Pigmentosum Complementation Group D Protein, Excision Repair Cross Complementing Rodent Repair Deficiency, Group 2 Protein
| xeroderma pigmentosum |
a rare genetic condition characterized by an eruption of exposed skin occurring in childhood and photosensitivity with severe sunburn; inherited as a recessive autosomal trait in which DNA repair processes are defective so they are more likely to chromosome breaks and cancers when exposed to ultraviolet light
출처: wordnet.princeton.edu/perl/webwn
|
|---|---|
| xeroderma pigmentosum |
a genetic disorder in which the skin is extremely sensitive to sunlight, causing it to age prematurely and leaving the individual particularly susceptible to skin cancer
출처: www.american-depot.com/services/resources_gl_x.asp
|
| xeroderma pigmentosum |
A disease in human beings caused by a defect in the UV mutation repair system.
출처: helios.bto.ed.ac.uk/bto/glossary/tuvwxyz.htm
|
| xeroderma pigmentosum |
An inherited disorder that causes extreme sensitivity to sunlight and early onset of skin cancers, including basal and squamous cell and melanoma. Patients are also at risk for cancers of the brain, lung, stomach, tongue, and melanoma of the eye, and leukemia.
출처: www.vh.org/adult/patient/cancercenter/prevention/p...
|
| xeroderma pigmentosum |
A genetic condition characterized by a sensitivity to all sources of ultraviolet radiation.
출처: goldbamboo.com/glossary-1x.html
|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|