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Ichthyosis Vulgaris
Most common form of ICHTHYOSIS characterized by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait.
推出的年份: 1991
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:
C16.131.831.512.410, C16.320.850.405, C17.800.428.333.410, C17.800.804.512.410, C17.800.827.405
MeSH 单一 ID:
D016112
进入的组:
Ichthyosis Simplex
Ichthyosis Simplices
Ichthyosis Vulgaris, Dominant
Dominant Ichthyosis Vulgaris
早前的内容:
Ichthyosis (1966-1990)
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Skin Abnormalities [C16.131.831]
Ichthyosis [C16.131.831.512]
Ichthyosiform Erythroderma, Congenital [C16.131.831.512.400]
add_circle
Ichthyosis Bullosa of Siemens [C16.131.831.512.408]
Ichthyosis Vulgaris [C16.131.831.512.410]
Ichthyosis, X-Linked [C16.131.831.512.420]
Sjogren-Larsson Syndrome [C16.131.831.512.723]
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]
add_circle
Ehlers-Danlos Syndrome [C16.320.850.260]
Epidermolysis Bullosa [C16.320.850.275]
add_circle
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]
Keratosis [C17.800.428]
Ichthyosis [C17.800.428.333]
Ichthyosiform Erythroderma, Congenital [C17.800.428.333.250]
add_circle
Ichthyosis Bullosa of Siemens [C17.800.428.333.330]
Ichthyosis Vulgaris [C17.800.428.333.410]
Ichthyosis, X-Linked [C17.800.428.333.420]
Sjogren-Larsson Syndrome [C17.800.428.333.723]
All MeSH Categories
Diseases Category
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Skin Abnormalities [C17.800.804]
Ichthyosis [C17.800.804.512]
Ichthyosiform Erythroderma, Congenital [C17.800.804.512.400]
add_circle
Ichthyosis Bullosa of Siemens [C17.800.804.512.405]
Ichthyosis Vulgaris [C17.800.804.512.410]
Ichthyosis, X-Linked [C17.800.804.512.420]
Sjogren-Larsson Syndrome [C17.800.804.512.723]
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]
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