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Xeroderma Pigmentosum
A rare, pigmentary, and atrophic autosomal recessive disease. It is manifested as an extreme photosensitivity to ULTRAVIOLET RAYS as the result of a deficiency in the enzyme that permits excisional repair of ultraviolet-damaged DNA.
推出的年份: 1963
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
congenital
diagnosis
diagnostic imaging
diet therapy
drug therapy
economics
embryology
enzymology
epidemiology
ethnology
etiology
genetics
history
immunology
metabolism
microbiology
mortality
nursing
parasitology
pathology
physiopathology
prevention and control
psychology
radiotherapy
rehabilitation
surgery
therapy
urine
veterinary
virology
树号:
C04.834.867, C16.131.831.936, C16.320.850.970, C17.800.600.925, C17.800.621.936, C17.800.804.936, C17.800.827.970, C18.452.284.975
MeSH 单一 ID:
D014983
进入的组:
Kaposi's Disease
Kaposis Disease
Kaposi Disease
All MeSH Categories
Diseases Category
Neoplasms [C04]
Precancerous Conditions [C04.834]
Aberrant Crypt Foci [C04.834.020]
Barrett Esophagus [C04.834.154]
Erythroplasia [C04.834.288]
Keratosis, Actinic [C04.834.450]
Leukoplakia [C04.834.512]
add_circle
Lymphomatoid Granulomatosis [C04.834.567]
Preleukemia [C04.834.770]
Smoldering Multiple Myeloma [C04.834.794]
Uterine Cervical Dysplasia [C04.834.818]
add_circle
Xeroderma Pigmentosum [C04.834.867]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Skin Abnormalities [C16.131.831]
Acrodermatitis [C16.131.831.066]
Carney Complex [C16.131.831.108]
Dyskeratosis Congenita [C16.131.831.150]
Ectodermal Dysplasia [C16.131.831.350]
add_circle
Ehlers-Danlos Syndrome [C16.131.831.428]
Epidermolysis Bullosa [C16.131.831.493]
add_circle
Ichthyosis [C16.131.831.512]
add_circle
Incontinentia Pigmenti [C16.131.831.580]
Port-Wine Stain [C16.131.831.675]
Prolidase Deficiency [C16.131.831.720]
Pseudoxanthoma Elasticum [C16.131.831.766]
Rothmund-Thomson Syndrome [C16.131.831.775]
Sclerema Neonatorum [C16.131.831.812]
Trichothiodystrophy Syndromes [C16.131.831.874]
Xeroderma Pigmentosum [C16.131.831.936]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Skin Diseases, Genetic [C16.320.850]
Albinism [C16.320.850.080]
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Cutis Laxa [C16.320.850.180]
Darier Disease [C16.320.850.190]
Dermatitis, Atopic [C16.320.850.210]
Dyskeratosis Congenita [C16.320.850.235]
Ectodermal Dysplasia [C16.320.850.250]
add_circle
Ehlers-Danlos Syndrome [C16.320.850.260]
Epidermolysis Bullosa [C16.320.850.275]
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Erythrokeratodermia Variabilis [C16.320.850.337]
Hyalinosis, Systemic [C16.320.850.368]
Ichthyosiform Erythroderma, Congenital [C16.320.850.400]
add_circle
Ichthyosis Bullosa of Siemens [C16.320.850.402]
Ichthyosis Vulgaris [C16.320.850.405]
Ichthyosis, X-Linked [C16.320.850.408]
Incontinentia Pigmenti [C16.320.850.420]
Keratoderma, Palmoplantar [C16.320.850.475]
add_circle
Leukokeratosis, Hereditary Mucosal [C16.320.850.542]
Lipoid Proteinosis of Urbach and Wiethe [C16.320.850.595]
Monilethrix [C16.320.850.647]
Netherton Syndrome [C16.320.850.673]
Pemphigus, Benign Familial [C16.320.850.700]
Porokeratosis [C16.320.850.730]
Porphyria, Erythropoietic [C16.320.850.738]
Porphyrias, Hepatic [C16.320.850.742]
add_circle
Prolidase Deficiency [C16.320.850.746]
Pseudoxanthoma Elasticum [C16.320.850.750]
Rothmund-Thomson Syndrome [C16.320.850.765]
Sjogren-Larsson Syndrome [C16.320.850.820]
Trichothiodystrophy Syndromes [C16.320.850.895]
Xeroderma Pigmentosum [C16.320.850.970]
All MeSH Categories
Diseases Category
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Photosensitivity Disorders [C17.800.600]
Dermatitis, Photoallergic [C17.800.600.325]
Dermatitis, Phototoxic [C17.800.600.335]
Hydroa Vacciniforme [C17.800.600.425]
Sunburn [C17.800.600.725]
Xeroderma Pigmentosum [C17.800.600.925]
All MeSH Categories
Diseases Category
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Pigmentation Disorders [C17.800.621]
Argyria [C17.800.621.166]
Cafe-au-Lait Spots [C17.800.621.250]
Hyperpigmentation [C17.800.621.430]
add_circle
Hypopigmentation [C17.800.621.440]
add_circle
Incontinentia Pigmenti [C17.800.621.497]
Urticaria Pigmentosa [C17.800.621.893]
Xeroderma Pigmentosum [C17.800.621.936]
Yellow Nail Syndrome [C17.800.621.968]
All MeSH Categories
Diseases Category
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Skin Abnormalities [C17.800.804]
Acrodermatitis [C17.800.804.066]
Anetoderma [C17.800.804.108]
Dyskeratosis Congenita [C17.800.804.150]
Ectodermal Dysplasia [C17.800.804.350]
add_circle
Ehlers-Danlos Syndrome [C17.800.804.428]
Epidermolysis Bullosa [C17.800.804.493]
add_circle
Ichthyosis [C17.800.804.512]
add_circle
Incontinentia Pigmenti [C17.800.804.580]
Port-Wine Stain [C17.800.804.675]
Pseudoxanthoma Elasticum [C17.800.804.766]
Rothmund-Thomson Syndrome [C17.800.804.775]
Sclerema Neonatorum [C17.800.804.812]
Trichothiodystrophy Syndromes [C17.800.804.874]
Xeroderma Pigmentosum [C17.800.804.936]
All MeSH Categories
Diseases Category
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Skin Diseases, Genetic [C17.800.827]
Albinism [C17.800.827.080]
add_circle
Cutis Laxa [C17.800.827.180]
Darier Disease [C17.800.827.190]
Dermatitis, Atopic [C17.800.827.210]
Dyskeratosis Congenita [C17.800.827.235]
Ectodermal Dysplasia [C17.800.827.250]
add_circle
Ehlers-Danlos Syndrome [C17.800.827.260]
Epidermolysis Bullosa [C17.800.827.275]
add_circle
Erythrokeratodermia Variabilis [C17.800.827.337]
Hereditary Autoinflammatory Diseases [C17.800.827.368]
add_circle
Hyalinosis, Systemic [C17.800.827.384]
Ichthyosiform Erythroderma, Congenital [C17.800.827.400]
add_circle
Ichthyosis Bullosa of Siemens [C17.800.827.403]
Ichthyosis Vulgaris [C17.800.827.405]
Ichthyosis, X-Linked [C17.800.827.408]
Incontinentia Pigmenti [C17.800.827.420]
Keratoderma, Palmoplantar [C17.800.827.475]
add_circle
Leukokeratosis, Hereditary Mucosal [C17.800.827.595]
Monilethrix [C17.800.827.602]
Muir-Torre Syndrome [C17.800.827.610]
Netherton Syndrome [C17.800.827.655]
Pemphigus, Benign Familial [C17.800.827.700]
Porokeratosis [C17.800.827.730]
Porphyria, Erythropoietic [C17.800.827.738]
Porphyrias, Hepatic [C17.800.827.742]
add_circle
Pseudoxanthoma Elasticum [C17.800.827.750]
Rothmund-Thomson Syndrome [C17.800.827.775]
Sjogren-Larsson Syndrome [C17.800.827.820]
Trichothiodystrophy Syndromes [C17.800.827.895]
Xeroderma Pigmentosum [C17.800.827.970]
All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
DNA Repair-Deficiency Disorders [C18.452.284]
Ataxia Telangiectasia [C18.452.284.060]
Bloom Syndrome [C18.452.284.100]
Cockayne Syndrome [C18.452.284.250]
Colorectal Neoplasms, Hereditary Nonpolyposis [C18.452.284.255]
Fanconi Anemia [C18.452.284.280]
Li-Fraumeni Syndrome [C18.452.284.520]
Nijmegen Breakage Syndrome [C18.452.284.600]
Rothmund-Thomson Syndrome [C18.452.284.760]
Severe Combined Immunodeficiency [C18.452.284.800]
Werner Syndrome [C18.452.284.960]
Xeroderma Pigmentosum [C18.452.284.975]
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