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Descriptor English: Genetic Diseases, X-Linked
Descriptor Spanish: Enfermedades Genéticas Ligadas al Cromosoma X
Descriptor enfermedades genéticas ligadas al cromosoma X
Entry term(s) enfermedades genéticas ligadas al X
Scope note: Enfermedades genéticas que estan ligadas a mutaciones en genes del CROMOSOMA X de los seres humanos (CROMOSOMA X HUMANO) o al CROMOSOMA X de otras especies. En este concepto se incluyen los modelos animales de enfermedades humanas ligadas al cromosoma X.
Descriptor Portuguese: Doenças Genéticas Ligadas ao Cromossomo X
Descriptor French: Maladies génétiques liées au chromosome X
Entry term(s): Disease, X-Linked Genetic
Diseases, X-Linked Genetic
Genetic Disease, X-Linked
Genetic Diseases, X Chromosome Linked
Genetic Diseases, X Linked
Genetic Diseases, X-Chromosome Linked
X Linked Genetic Diseases
X-Linked Genetic Disease
X-Linked Genetic Diseases
Tree number(s): C16.320.322
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D040181
Scope note: 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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Genetic Diseases, Inborn (1966-2002)
Linkage (Genetics) (1984-2002)
specific disease/Genetics (1984-2002)
Public MeSH Note: 2003
History Note: 2003
Entry Version: GENET DIS X LINKED
Related: Chromosomes, Human, X MeSH
Genes, X-Linked MeSH
Sex Chromosome Aberrations MeSH
Sex Chromosome Disorders MeSH
DeCS ID: 37289
Unique ID: D040181
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2003/01/01
Date of Entry: 2002/07/03
Revision Date: 2013/07/09
Genetic Diseases, X-Linked - Preferred
Concept UI M0420489
Scope note 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.
Preferred term Genetic Diseases, X-Linked
Entry term(s) Disease, X-Linked Genetic
Diseases, X-Linked Genetic
Genetic Disease, X-Linked
Genetic Diseases, X Chromosome Linked
Genetic Diseases, X Linked
Genetic Diseases, X-Chromosome Linked
X Linked Genetic Diseases
X-Linked Genetic Disease
X-Linked Genetic Diseases



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