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Albinism
General term for a number of inherited defects of amino acid metabolism in which there is a deficiency or absence of pigment in the eyes, skin, or hair.
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
radiotherapy
rehabilitation
surgery
therapy
urine
veterinary
virology
树号:
C11.270.040, C16.320.290.040, C16.320.565.100.102, C16.320.850.080, C17.800.621.440.102, C17.800.827.080, C18.452.648.100.102
MeSH 单一 ID:
D000417
All MeSH Categories
Diseases Category
Eye Diseases [C11]
Eye Diseases, Hereditary [C11.270]
Aicardi Syndrome [C11.270.019]
Albinism [C11.270.040]
Albinism, Ocular [C11.270.040.090]
Albinism, Oculocutaneous [C11.270.040.545]
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Chediak-Higashi Syndrome [C11.270.040.772]
add_circle
Aniridia [C11.270.060]
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Choroideremia [C11.270.142]
Coloboma [C11.270.147]
add_circle
Cone Dystrophy [C11.270.151]
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Cone-Rod Dystrophies [C11.270.152]
Corneal Dystrophies, Hereditary [C11.270.162]
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Duane Retraction Syndrome [C11.270.235]
Familial Exudative Vitreoretinopathies [C11.270.238]
Graves Ophthalmopathy [C11.270.240]
Gyrate Atrophy [C11.270.468]
Leber Congenital Amaurosis [C11.270.516]
Optic Atrophies, Hereditary [C11.270.564]
add_circle
Optic Nerve Hypoplasia [C11.270.588]
Retinal Degeneration [C11.270.612]
Retinal Dysplasia [C11.270.660]
Retinitis Pigmentosa [C11.270.684]
add_circle
Retinoblastoma [C11.270.862]
Stargardt Disease [C11.270.872]
Walker-Warburg Syndrome [C11.270.881]
Weill-Marchesani Syndrome [C11.270.921]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Eye Diseases, Hereditary [C16.320.290]
Aicardi Syndrome [C16.320.290.019]
Albinism [C16.320.290.040]
Albinism, Ocular [C16.320.290.040.090]
Albinism, Oculocutaneous [C16.320.290.040.100]
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Piebaldism [C16.320.290.040.600]
Aniridia [C16.320.290.078]
add_circle
Choroideremia [C16.320.290.142]
Cone-Rod Dystrophies [C16.320.290.152]
Corneal Dystrophies, Hereditary [C16.320.290.162]
add_circle
Duane Retraction Syndrome [C16.320.290.235]
Familial Exudative Vitreoretinopathies [C16.320.290.352]
Graves Ophthalmopathy [C16.320.290.410]
Gyrate Atrophy [C16.320.290.468]
Optic Atrophies, Hereditary [C16.320.290.564]
add_circle
Optic Nerve Hypoplasia [C16.320.290.612]
Retinal Dysplasia [C16.320.290.660]
Retinitis Pigmentosa [C16.320.290.684]
add_circle
Stargardt Disease [C16.320.290.724]
Vitelliform Macular Dystrophy [C16.320.290.763]
Weill-Marchesani Syndrome [C16.320.290.842]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Amino Acid Metabolism, Inborn Errors [C16.320.565.100]
Albinism [C16.320.565.100.102]
Albinism, Ocular [C16.320.565.100.102.090]
Albinism, Oculocutaneous [C16.320.565.100.102.100]
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Piebaldism [C16.320.565.100.102.600]
Alkaptonuria [C16.320.565.100.187]
Hyperglycinemia, Nonketotic [C16.320.565.100.477]
Hyperhomocysteinemia [C16.320.565.100.480]
add_circle
Hyperlysinemias [C16.320.565.100.544]
Maple Syrup Urine Disease [C16.320.565.100.608]
Multiple Acyl Coenzyme A Dehydrogenase Deficiency [C16.320.565.100.614]
Multiple Carboxylase Deficiency [C16.320.565.100.620]
add_circle
Phenylketonurias [C16.320.565.100.766]
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Prolidase Deficiency [C16.320.565.100.794]
Propionic Acidemia [C16.320.565.100.823]
Tyrosinemias [C16.320.565.100.880]
Urea Cycle Disorders, Inborn [C16.320.565.100.940]
add_circle
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]
Albinism, Ocular [C16.320.850.080.090]
Albinism, Oculocutaneous [C16.320.850.080.100]
add_circle
Piebaldism [C16.320.850.080.600]
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]
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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]
Pigmentation Disorders [C17.800.621]
Hypopigmentation [C17.800.621.440]
Albinism [C17.800.621.440.102]
Albinism, Ocular [C17.800.621.440.102.090]
Albinism, Oculocutaneous [C17.800.621.440.102.100]
add_circle
Piebaldism [C17.800.621.440.102.600]
Vitiligo [C17.800.621.440.895]
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]
Albinism, Ocular [C17.800.827.080.090]
Albinism, Oculocutaneous [C17.800.827.080.100]
add_circle
Piebaldism [C17.800.827.080.600]
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]
Metabolism, Inborn Errors [C18.452.648]
Amino Acid Metabolism, Inborn Errors [C18.452.648.100]
Albinism [C18.452.648.100.102]
Albinism, Ocular [C18.452.648.100.102.090]
Albinism, Oculocutaneous [C18.452.648.100.102.100]
add_circle
Piebaldism [C18.452.648.100.102.600]
Alkaptonuria [C18.452.648.100.187]
Hyperglycinemia, Nonketotic [C18.452.648.100.477]
Hyperhomocysteinemia [C18.452.648.100.480]
add_circle
Hyperlysinemias [C18.452.648.100.544]
Maple Syrup Urine Disease [C18.452.648.100.608]
Multiple Acyl Coenzyme A Dehydrogenase Deficiency [C18.452.648.100.614]
Multiple Carboxylase Deficiency [C18.452.648.100.620]
add_circle
Phenylketonurias [C18.452.648.100.766]
add_circle
Propionic Acidemia [C18.452.648.100.823]
Tyrosinemias [C18.452.648.100.880]
Urea Cycle Disorders, Inborn [C18.452.648.100.940]
add_circle
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