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Epidermolysis Bullosa
Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties.
推出的年份:
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
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
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urine
veterinary
virology
树号:
C16.131.831.493, C16.320.850.275, C17.800.804.493, C17.800.827.275, C17.800.865.410
MeSH 单一 ID:
D004820
进入的组:
Acantholysis Bullosa
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]
Epidermolysis Bullosa Acquisita [C16.131.831.493.080]
Epidermolysis Bullosa Dystrophica [C16.131.831.493.160]
Epidermolysis Bullosa Simplex [C16.131.831.493.180]
Epidermolysis Bullosa, Junctional [C16.131.831.493.170]
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]
add_circle
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]
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Ehlers-Danlos Syndrome [C16.320.850.260]
Epidermolysis Bullosa [C16.320.850.275]
Epidermolysis Bullosa Dystrophica [C16.320.850.275.160]
Epidermolysis Bullosa Simplex [C16.320.850.275.180]
Epidermolysis Bullosa, Junctional [C16.320.850.275.170]
Erythrokeratodermia Variabilis [C16.320.850.337]
Hyalinosis, Systemic [C16.320.850.368]
Ichthyosiform Erythroderma, Congenital [C16.320.850.400]
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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]
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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]
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]
Epidermolysis Bullosa Acquisita [C17.800.804.493.080]
Epidermolysis Bullosa Dystrophica [C17.800.804.493.160]
Epidermolysis Bullosa Simplex [C17.800.804.493.180]
Epidermolysis Bullosa, Junctional [C17.800.804.493.170]
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]
Epidermolysis Bullosa Acquisita [C17.800.827.275.080]
Epidermolysis Bullosa Dystrophica [C17.800.827.275.160]
Epidermolysis Bullosa Simplex [C17.800.827.275.180]
Epidermolysis Bullosa, Junctional [C17.800.827.275.170]
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
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Skin Diseases, Vesiculobullous [C17.800.865]
Acantholysis [C17.800.865.070]
Blister [C17.800.865.187]
Dermatitis Herpetiformis [C17.800.865.360]
Eczema, Dyshidrotic [C17.800.865.385]
Epidermolysis Bullosa [C17.800.865.410]
Epidermolysis Bullosa Acquisita [C17.800.865.410.080]
Epidermolysis Bullosa Dystrophica [C17.800.865.410.160]
Epidermolysis Bullosa Simplex [C17.800.865.410.180]
Epidermolysis Bullosa, Junctional [C17.800.865.410.170]
Erythema Multiforme [C17.800.865.475]
add_circle
Hydroa Vacciniforme [C17.800.865.575]
Linear IgA Bullous Dermatosis [C17.800.865.622]
Pemphigoid Gestationis [C17.800.865.700]
Pemphigoid, Benign Mucous Membrane [C17.800.865.670]
Pemphigoid, Bullous [C17.800.865.690]
Pemphigus [C17.800.865.716]
Pemphigus, Benign Familial [C17.800.865.858]
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