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Mental Retardation, X-Linked
A class of genetic disorders resulting in INTELLECTUAL DISABILITY that is associated either with mutations of GENES located on the X CHROMOSOME or aberrations in the structure of the X chromosome (SEX CHROMOSOME ABERRATIONS).
推出的年份: 2003
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:
C10.597.606.360.455, C16.320.322.500, C16.320.400.525
MeSH 单一 ID:
D038901
进入的组:
Mental Retardation, X Linked
Retardation, X-Linked Mental
X-Linked Mental Retardations
X-Linked Mental Retardation Syndromes
X Linked Mental Retardation Syndromes
X-Linked Mental Retardation Disorders
X Linked Mental Retardation Disorders
X-Linked Mental Retardation
X Linked Mental Retardation
早前的内容:
Mental Retardation/genetics (1971-2002)
All MeSH Categories
Diseases Category
Nervous System Diseases [C10]
Neurologic Manifestations [C10.597]
Neurobehavioral Manifestations [C10.597.606]
Intellectual Disability [C10.597.606.360]
Cri-du-Chat Syndrome [C10.597.606.360.180]
De Lange Syndrome [C10.597.606.360.210]
Down Syndrome [C10.597.606.360.220]
Mental Retardation, X-Linked [C10.597.606.360.455]
Adrenoleukodystrophy [C10.597.606.360.455.124]
Coffin-Lowry Syndrome [C10.597.606.360.455.249]
Fragile X Syndrome [C10.597.606.360.455.500]
Glycogen Storage Disease Type IIb [C10.597.606.360.455.562]
Lesch-Nyhan Syndrome [C10.597.606.360.455.625]
Menkes Kinky Hair Syndrome [C10.597.606.360.455.687]
Mucopolysaccharidosis II [C10.597.606.360.455.750]
Pyruvate Dehydrogenase Complex Deficiency Disease [C10.597.606.360.455.875]
Rett Syndrome [C10.597.606.360.455.937]
Prader-Willi Syndrome [C10.597.606.360.690]
Rubinstein-Taybi Syndrome [C10.597.606.360.700]
Trisomy 13 Syndrome [C10.597.606.360.835]
WAGR Syndrome []
add_circle
Williams Syndrome [C10.597.606.360.970]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Genetic Diseases, X-Linked [C16.320.322]
Aicardi Syndrome [C16.320.322.030]
Androgen-Insensitivity Syndrome [C16.320.322.061]
Barth Syndrome [C16.320.322.068]
Bulbo-Spinal Atrophy, X-Linked [C16.320.322.076]
Choroideremia [C16.320.322.092]
Dent Disease [C16.320.322.100]
Dyskeratosis Congenita [C16.320.322.108]
Ectodermal Dysplasia 1, Anhidrotic [C16.320.322.116]
Fabry Disease [C16.320.322.124]
Focal Dermal Hypoplasia [C16.320.322.186]
Glycogen Storage Disease Type IIb [C16.320.322.201]
Glycogen Storage Disease Type VIII [C16.320.322.217]
Granulomatous Disease, Chronic [C16.320.322.233]
Hemophilia B [C16.320.322.235]
Hyper-IgM Immunodeficiency Syndrome, Type 1 [C16.320.322.237]
Ichthyosis, X-Linked [C16.320.322.241]
Isolated Noncompaction of the Ventricular Myocardium [C16.320.322.370]
Mental Retardation, X-Linked [C16.320.322.500]
Adrenoleukodystrophy [C16.320.322.500.124]
Classical Lissencephalies and Subcortical Band Heterotopias [C16.320.322.500.186]
Coffin-Lowry Syndrome [C16.320.322.500.249]
Fragile X Syndrome [C16.320.322.500.500]
Lesch-Nyhan Syndrome [C16.320.322.500.625]
Menkes Kinky Hair Syndrome [C16.320.322.500.687]
Mucopolysaccharidosis II [C16.320.322.500.750]
Pyruvate Dehydrogenase Complex Deficiency Disease [C16.320.322.500.875]
Rett Syndrome [C16.320.322.500.937]
Muscular Dystrophy, Duchenne [C16.320.322.562]
Muscular Dystrophy, Emery-Dreifuss [C16.320.322.625]
add_circle
Oculocerebrorenal Syndrome [C16.320.322.750]
Ornithine Carbamoyltransferase Deficiency Disease [C16.320.322.828]
Pelizaeus-Merzbacher Disease [C16.320.322.906]
Wiskott-Aldrich Syndrome [C16.320.322.937]
X-Linked Combined Immunodeficiency Diseases [C16.320.322.968]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Heredodegenerative Disorders, Nervous System [C16.320.400]
Alexander Disease [C16.320.400.024]
Amyloid Neuropathies, Familial [C16.320.400.050]
Bulbo-Spinal Atrophy, X-Linked [C16.320.400.100]
Canavan Disease [C16.320.400.150]
Cockayne Syndrome [C16.320.400.200]
Dystonia Musculorum Deformans [C16.320.400.330]
Gerstmann-Straussler-Scheinker Disease [C16.320.400.350]
Hepatolenticular Degeneration [C16.320.400.361]
Hereditary Central Nervous System Demyelinating Diseases [C16.320.400.367]
Hereditary Sensory and Autonomic Neuropathies [C16.320.400.415]
add_circle
Hereditary Sensory and Motor Neuropathy [C16.320.400.375]
add_circle
Huntington Disease [C16.320.400.430]
Lafora Disease [C16.320.400.480]
Mental Retardation, X-Linked [C16.320.400.525]
Adrenoleukodystrophy [C16.320.400.525.124]
Coffin-Lowry Syndrome [C16.320.400.525.249]
Fragile X Syndrome [C16.320.400.525.500]
Lesch-Nyhan Syndrome [C16.320.400.525.625]
Menkes Kinky Hair Syndrome [C16.320.400.525.687]
Mucopolysaccharidosis II [C16.320.400.525.750]
Pyruvate Dehydrogenase Complex Deficiency Disease [C16.320.400.525.875]
Rett Syndrome [C16.320.400.525.937]
Myotonia Congenita [C16.320.400.540]
Myotonic Dystrophy [C16.320.400.542]
Neuroacanthocytosis [C16.320.400.550]
Neurofibromatoses [C16.320.400.560]
add_circle
Neuronal Ceroid-Lipofuscinoses [C16.320.400.600]
Optic Atrophies, Hereditary [C16.320.400.630]
add_circle
Pantothenate Kinase-Associated Neurodegeneration [C16.320.400.650]
Spinal Muscular Atrophies of Childhood [C16.320.400.765]
Spinocerebellar Degenerations [C16.320.400.780]
add_circle
Tourette Syndrome [C16.320.400.820]
Tuberous Sclerosis [C16.320.400.880]
Unverricht-Lundborg Syndrome [C16.320.400.940]
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