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Ichthyosis, X-Linked MeSH Descriptor Data 2022


MeSH Heading
Ichthyosis, X-Linked
Tree Number(s)
C16.131.831.512.420
C16.320.322.241
C16.320.565.925.400
C16.320.850.408
C16.614.492.420
C17.800.428.333.420
C17.800.804.512.420
C17.800.827.408
C18.452.648.925.400
Unique ID
D016114
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D016114
Annotation
do not use /‌congen & do not coord with INFANT, NEWBORN, DISEASES
Scope Note
Chronic form of ichthyosis that is inherited as a sex-linked recessive trait carried on the X-chromosome and transmitted to the male offspring. It is characterized by severe scaling, especially on the extremities, and is associated with steroid sulfatase deficiency.
Entry Term(s)
Ichthyosis, Sex-Linked
Placental Steroid Sulfatase Deficiency
Steroid Sulfatase Deficiency
Steroid Sulfatase Deficiency Disease
Previous Indexing
Ichthyosis (1966-1990)
See Also
Steryl-Sulfatase
Public MeSH Note
91
History Note
91
Date Established
1991/01/01
Date of Entry
1990/02/12
Revision Date
2015/06/18
Ichthyosis, X-Linked Preferred
Placental Steroid Sulfatase Deficiency Related
Steroid Sulfatase Deficiency Disease Narrower
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