Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Steroid Metabolism, Inborn Errors
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Steroid Metabolism, Inborn Errors
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Preferred term
Ichthyosis, X-Linked
Type
-
Topical Descriptor
Broader concept
Entry terms
- Ichthyoses, Sex-Linked
- Ichthyosis, Sex Linked
- Ichthyosis, Sex-Linked
Note
- 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.
History note
- 91
In other languages
-
Finnish
-
ichthyosis congenita recessiva chromosomate X dependens
-
ichtyosis congenita recessiva
-
X-kromosomissa periytyvä iktyoosi
-
X-sidonnainen iktyoosi
-
X-sidonnainen kalansuomutauti
-
Swedish
URI
http://www.yso.fi/onto/mesh/D016114
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