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Genetic Diseases, X-Linked
MeSH HeadingGenetic Diseases, X-Linked
Tree NumberC16.320.322
Scope NoteGenetic diseases that are linked to gene mutations on the X CHROMOSOME in humans (X CHROMOSOME, HUMAN) or the X CHROMOSOME in other species. Included here are animal models of human X-linked diseases.
Entry TermGenetic Diseases, X-Chromosome Linked
Entry TermX-Linked Genetic Diseases
See AlsoChromosomes, Human, X
See AlsoGenes, X-Linked
See AlsoSex Chromosome Aberrations
See AlsoSex Chromosome Disorders
Allowable QualifiersBL CF CI CL CO DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RA RH RI RT SU TH UR US VE VI
Entry VersionGENET DIS X LINKED
Previous Indexing Genetic Diseases, Inborn (1966-2002)
Previous IndexingLinkage (Genetics) (1984-2002)
Previous Indexingspecific disease/Genetics (1984-2002)
History Note2003
Date of Entry20020703
Unique IDD040181


MeSH Tree Structures

 
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]  +
Anemia, Hypoplastic, Congenital [C16.320.077]  +
Angioedemas, Hereditary [C16.320.078]
Ataxia Telangiectasia [C16.320.080]
Autoimmune Lymphoproliferative Syndrome [C16.320.089]
Blood Coagulation Disorders, Inherited [C16.320.099]  +
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]  +
Costello Syndrome [C16.320.185]
Cystic Fibrosis [C16.320.190]
Donohue Syndrome [C16.320.215]
Dwarfism [C16.320.240]  +
Eye Diseases, Hereditary [C16.320.290]  +
Frasier Syndrome [C16.320.306]
Arrow pointing to current tree nodeGenetic 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]
Hypophosphatemic Rickets, X-Linked Dominant [C16.320.322.239]
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]  +
Muscular Dystrophy, Duchenne [C16.320.322.562]
Muscular Dystrophy, Emery-Dreifuss [C16.320.322.625]
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]
Genetic Diseases, Y-Linked [C16.320.338]
Hajdu-Cheney Syndrome [C16.320.355]
Hemoglobinopathies [C16.320.365]  +
Hereditary Autoinflammatory Diseases [C16.320.382]  +
Heredodegenerative Disorders, Nervous System [C16.320.400]  +
Hyperthyroxinemia, Familial Dysalbuminemic [C16.320.427]
Kallmann Syndrome [C16.320.467]
Kartagener Syndrome [C16.320.480]
Loeys-Dietz Syndrome [C16.320.510]
Marfan Syndrome [C16.320.540]
Metabolism, Inborn Errors [C16.320.565]  +
Muscular Dystrophies [C16.320.577]  +
Myasthenic Syndromes, Congenital [C16.320.590]
Nail-Patella Syndrome [C16.320.600]
Neoplastic Syndromes, Hereditary [C16.320.700]  +
Osteogenesis Imperfecta [C16.320.737]
Pain Insensitivity, Congenital [C16.320.775]
Pelger-Huet Anomaly [C16.320.784]
Polycystic Kidney, Autosomal Recessive [C16.320.793]
Pycnodysostosis [C16.320.812]
Skin Diseases, Genetic [C16.320.850]  +
Weill-Marchesani Syndrome [C16.320.887]
Werner Syndrome [C16.320.925]
Yellow Nail Syndrome [C16.320.962]

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