Structured Summary
Abstract
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.
MeSH Record
Classification
Broader headings
Narrower headings
- Aicardi Syndrome
- Androgen-Insensitivity Syndrome
- Anhidrotic Ectodermal Dysplasia 1
- Barth Syndrome
- Choroideremia
- Chronic Granulomatous Disease
- Dent Disease
- Duchenne Muscular Dystrophy
- Dyskeratosis Congenita
- Emery-Dreifuss Muscular Dystrophy
- Fabry Disease
- Focal Dermal Hypoplasia
- Glycogen Storage Disease Type IIb
- Glycogen Storage Disease Type VIII
- Hemophilia B
- Isolated Noncompaction of the Ventricular Myocardium
- Oculocerebrorenal Syndrome
- Ornithine Carbamoyltransferase Deficiency Disease
- Pelizaeus-Merzbacher Disease
- Type 1 Hyper-IgM Immunodeficiency Syndrome
- Wiskott-Aldrich Syndrome
- X-Linked Bulbo-Spinal Atrophy
- X-Linked Combined Immunodeficiency Diseases
- X-Linked Ichthyosis
- X-Linked Intellectual Disability
Related Concepts
Knowledge Graph
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MeSH Record
See Also
MeSH Record
Synonyms
9 entry terms
- Genetic Diseases, X-Chromosome Linked
- Genetic Diseases, X-Linked
- Disease, X-Linked Genetic
- Diseases, X-Linked Genetic
- Genetic Disease, X-Linked
- Genetic Diseases, X Chromosome Linked
- Genetic Diseases, X Linked
- X Linked Genetic Diseases
- X-Linked Genetic Disease
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings 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 & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2003
MeSH Record
Previous Indexing
- Genetic Diseases, Inborn (1966-2002)
- Linkage (Genetics) (1984-2002)
- specific disease/Genetics (1984-2002)
MeSH Hierarchy
Tree Number
AMA Style
References
- National Library of Medicine. X-Linked Genetic Diseases. Medical Subject Headings (MeSH). 2026. Unique ID D040181. http://id.nlm.nih.gov/mesh/2026/D040181
- X-Linked Genetic Diseases. In: Wikidata. https://www.wikidata.org/wiki/Q18553438