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The way concept relations are shown:
Ichthyosis, X-Linked
Hierarchy: | ∟ ∟ ∟ ∟ ∟ Ichthyosis, X-Linked 44 coordinate concepts∟ ∟ ∟ ∟ Ichthyosis, X-Linked 44 coordinate concepts∟ ∟ ∟ ∟ ∟ Ichthyosis, X-Linked 44 coordinate concepts∟ ∟ ∟ ∟ Ichthyosis, X-Linked 44 coordinate concepts∟ ∟ ∟ ∟ Ichthyosis, X-Linked 44 coordinate concepts∟ ∟ ∟ ∟ ∟ Ichthyosis, X-Linked 44 coordinate concepts∟ ∟ ∟ ∟ ∟ Ichthyosis, X-Linked 44 coordinate concepts∟ ∟ ∟ ∟ ∟ Ichthyosis, X-Linked 44 coordinate concepts∟ ∟ ∟ ∟ Ichthyosis, X-Linked 44 coordinate conceptsX |
Broader terms: | ∟ ∟ ∟ ∟ ∟ Ichthyosis, X-Linked ∟ ∟ ∟ ∟ Ichthyosis, X-Linked ∟ ∟ ∟ ∟ ∟ Ichthyosis, X-Linked ∟ ∟ ∟ ∟ Ichthyosis, X-Linked ∟ ∟ ∟ ∟ Ichthyosis, X-Linked ∟ ∟ ∟ ∟ ∟ Ichthyosis, X-Linked ∟ ∟ ∟ ∟ ∟ Ichthyosis, X-Linked ∟ ∟ ∟ ∟ ∟ Ichthyosis, X-Linked ∟ ∟ ∟ ∟ Ichthyosis, X-Linked |
Annotation: | do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
X |
History note: | Ichthyosis (1966-1990)X |
historyNote*: | 91
X |
publicMeSHNote*: | 91
X |
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.
X |
activeMeSHYear*: | 2007X |
dateCreated*: | 1990-02-12X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | AGSX |
Related term: | |
Type: | |
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Labels and equivalent concepts: | X-kromosomissa periytyvä kalansuomutauti (fi) XX-sidonnainen kalansuomutauti (fi, replaced) X-sidonnainen iktyoosi (fi, replaced) X-kromosomissa periytyvä iktyoosi (fi, replaced) Iktyos, X-bunden (sv) Ichthyosis, Sex-Linked (en, replaced) Ichtyosis congenita recessiva (la-FI, replaced) |
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