Käsitteen tiedot
Käytettävä termi
Genetic Diseases, X-Linked
Tyyppi
-
Topical Descriptor
Yläkäsite
Alakäsitteet
- Aicardi Syndrome
- Androgen-Insensitivity Syndrome
- Barth Syndrome
- Bulbo-Spinal Atrophy, X-Linked
- Choroideremia
- Dent Disease
- Dyskeratosis Congenita
- Ectodermal Dysplasia 1, Anhidrotic
- Fabry Disease
- Focal Dermal Hypoplasia
- Glycogen Storage Disease Type VIII
- Granulomatous Disease, Chronic
- Hemophilia B
- Hyper-IgM Immunodeficiency Syndrome, Type 1
- Ichthyosis, X-Linked
- Isolated Noncompaction of the Ventricular Myocardium
- Mental Retardation, X-Linked
- Muscular Dystrophy, Duchenne
- Muscular Dystrophy, Emery-Dreifuss
- Oculocerebrorenal Syndrome
- Ornithine Carbamoyltransferase Deficiency Disease
- Pelizaeus-Merzbacher Disease
- Wiskott-Aldrich Syndrome
- X-Linked Combined Immunodeficiency Diseases
Ohjaustermit
- Genetic Diseases, X Chromosome Linked
- Genetic Diseases, X-Chromosome Linked
- X Linked Genetic Diseases
- X-Linked Genetic Diseases
Käyttöhuomautus
- Genetic 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.
Huomautus muutoshistoriasta
- 2003
Muunkieliset termit
-
ruotsi
-
suomi
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X-kromosomissa periytyvä sairaus
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X-kromosomissa periytyvä tauti
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X-kromosomissa periytyvät sairaudet
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X-kromosomissa periytyvät taudit
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X-sidonnainen perinnöllinen sairaus
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X-sidonnainen perinnöllinen tauti
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X-sidonnaiset perinnölliset taudit
URI
http://www.yso.fi/onto/mesh/D040181
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