| Descriptor English: | Ichthyosis, X-Linked | ||||||
| Descriptor Spanish: |
Ictiosis Ligada al Cromosoma X
| ||||||
| Descriptor Portuguese: | Ictiose Ligada ao Cromossomo X | ||||||
| Descriptor French: | Ichtyose liée à l'X | ||||||
| Entry term(s): |
Deficiencies, Steroid Sulfatase Deficiency, Steroid Sulfatase Ichthyoses, Sex-Linked Ichthyoses, X-Linked Ichthyosis, Sex Linked Ichthyosis, Sex-Linked Ichthyosis, X Linked Placental Steroid Sulfatase Deficiency Steroid Sulfatase Deficiencies Steroid Sulfatase Deficiency Steroid Sulfatase Deficiency Disease Sulfatase Deficiencies, Steroid Sulfatase Deficiency, Steroid |
||||||
| 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 |
||||||
| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D016114 | ||||||
| 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. |
||||||
| Annotation: | do not use /congen & do not coord with INFANT, NEWBORN, 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: |
Ichthyosis (1966-1990) |
||||||
| Public MeSH Note: | 91 |
||||||
| History Note: | 91 |
||||||
| Related: |
Steryl-Sulfatase
MeSH | ||||||
| DeCS ID: | 28987 | ||||||
| Unique ID: | D016114 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| 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 but not broader or narrower
Steroid Sulfatase Deficiency Disease
- Narrower
| Concept UI |
M0024615 |
| 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. |
| Preferred term | Ichthyosis, X-Linked |
| Entry term(s) |
Ichthyoses, Sex-Linked Ichthyoses, X-Linked Ichthyosis, Sex Linked Ichthyosis, Sex-Linked Ichthyosis, X Linked |
| Concept UI |
M0536647 |
| Preferred term | Placental Steroid Sulfatase Deficiency |
| Entry term(s) |
Deficiencies, Steroid Sulfatase Deficiency, Steroid Sulfatase Steroid Sulfatase Deficiencies Steroid Sulfatase Deficiency Sulfatase Deficiencies, Steroid Sulfatase Deficiency, Steroid |
| Concept UI |
M0536355 |
| Preferred term | Steroid Sulfatase Deficiency Disease |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
