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Skin Diseases, Genetic
Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.
推出的年份: 1998
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
radiotherapy
rehabilitation
surgery
therapy
urine
veterinary
virology
树号:
C16.320.850, C17.800.827
MeSH 单一 ID:
D012873
进入的组:
Genetic Skin Diseases
Disease, Genetic Skin
Diseases, Genetic Skin
Genetic Skin Disease
Skin Disease, Genetic
早前的内容:
Skin Diseases (1975-1997)
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Adrenal Hyperplasia, Congenital [C16.320.033]
Alagille Syndrome [C16.320.051]
alpha 1-Antitrypsin Deficiency [C16.320.060]
Anemia, Hemolytic, Congenital [C16.320.070]
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Anemia, Hypoplastic, Congenital [C16.320.077]
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Ataxia Telangiectasia [C16.320.080]
Autoimmune Lymphoproliferative Syndrome [C16.320.089]
Blood Coagulation Disorders, Inherited [C16.320.099]
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Brugada Syndrome [C16.320.100]
CADASIL [C16.320.129]
Camurati-Engelmann Syndrome [C16.320.144]
Cardiomyopathy, Hypertrophic, Familial [C16.320.160]
CHARGE Syndrome [C16.320.165]
Cherubism [C16.320.170]
Chromosome Disorders [C16.320.180]
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Ciliopathies [C16.320.184]
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Costello Syndrome [C16.320.188]
Cystic Fibrosis [C16.320.190]
Donohue Syndrome [C16.320.215]
Dwarfism [C16.320.240]
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Eye Diseases, Hereditary [C16.320.290]
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Familial Multiple Lipomatosis [C16.320.298]
Frasier Syndrome [C16.320.306]
GATA2 Deficiency [C16.320.314]
Genetic Diseases, X-Linked [C16.320.322]
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Genetic Diseases, Y-Linked [C16.320.338]
Hajdu-Cheney Syndrome [C16.320.355]
Hemoglobinopathies [C16.320.365]
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Hereditary Autoinflammatory Diseases [C16.320.382]
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Heredodegenerative Disorders, Nervous System [C16.320.400]
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Hyper-IgM Immunodeficiency Syndrome [C16.320.413]
Hyperthyroxinemia, Familial Dysalbuminemic [C16.320.427]
Kallmann Syndrome [C16.320.467]
Kartagener Syndrome [C16.320.184.500.531]
Laminopathies [C16.320.488]
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Lennox Gastaut Syndrome [C16.320.495]
Loeys-Dietz Syndrome [C16.320.510]
Marfan Syndrome [C16.320.540]
Metabolism, Inborn Errors [C16.320.565]
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Muscular Dystrophies [C16.320.577]
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Myasthenic Syndromes, Congenital [C16.320.590]
Nail-Patella Syndrome [C16.320.600]
Neoplastic Syndromes, Hereditary [C16.320.700]
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Oculocerebrorenal Syndrome [C16.320.322.750]
Orofaciodigital Syndromes [C16.320.180.830.670]
Osteoarthropathy, Primary Hypertrophic [C16.320.718]
Osteochondrodysplasias [C16.320.728]
Osteogenesis Imperfecta [C16.320.737]
Pain Insensitivity, Congenital [C16.320.775]
Pelger-Huet Anomaly [C16.320.784]
Primary Immunodeficiency Diseases [C16.320.798]
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Pycnodysostosis [C16.320.565.595.800]
Renal Tubular Transport, Inborn Errors [C16.320.565.893]
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]
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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]
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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]
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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]
Werner Syndrome [C16.320.925]
Yellow Nail Syndrome [C16.320.962]
All MeSH Categories
Diseases Category
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Acneiform Eruptions [C17.800.030]
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Angiolymphoid Hyperplasia with Eosinophilia [C17.800.060]
Breast Diseases [C17.800.090]
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Cutaneous Fistula [C17.800.135]
Dermatitis [C17.800.174]
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Dermatomyositis [C17.800.185]
Erythema [C17.800.229]
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Exanthema [C17.800.257]
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Facial Dermatoses [C17.800.271]
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Foot Diseases [C17.800.321]
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Hair Diseases [C17.800.329]
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Hand Dermatoses [C17.800.338]
Keratoacanthoma [C17.800.417]
Keratosis [C17.800.428]
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Leg Dermatoses [C17.800.446]
Lipomatosis [C17.800.463]
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Lupus Erythematosus, Cutaneous [C17.800.480]
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Morgellons Disease [C17.800.518]
Nail Diseases [C17.800.529]
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Necrobiotic Disorders [C17.800.550]
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Necrolytic Migratory Erythema [C17.800.551]
Nephrogenic Fibrosing Dermopathy [C17.800.553]
Panniculitis [C17.800.566]
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Photosensitivity Disorders [C17.800.600]
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Pigmentation Disorders [C17.800.621]
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Prurigo [C17.800.674]
Pruritus [C17.800.685]
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Pyoderma [C17.800.695]
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Rosacea [C17.800.716]
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Scalp Dermatoses [C17.800.738]
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Scleredema Adultorum [C17.800.751]
Scleroderma, Localized [C17.800.767]
Scleroderma, Systemic [C17.800.784]
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Sebaceous Gland Diseases [C17.800.794]
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Skin Abnormalities [C17.800.804]
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Skin Diseases, Eczematous [C17.800.815]
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Skin Diseases, Genetic [C17.800.827]
Albinism [C17.800.827.080]
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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]
Skin Diseases, Infectious [C17.800.838]
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Skin Diseases, Metabolic [C17.800.849]
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Skin Diseases, Papulosquamous [C17.800.859]
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Skin Diseases, Vascular [C17.800.862]
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Skin Diseases, Vesiculobullous [C17.800.865]
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Skin Neoplasms [C17.800.882]
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Skin Ulcer [C17.800.893]
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Sweat Gland Diseases [C17.800.946]
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Xanthogranuloma, Juvenile [C17.800.973]
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