| Descriptor English: | Ectodermal Dysplasia 1, Anhidrotic | ||||||
| Descriptor Spanish: |
Displasia Ectodermal Anhidrótica Tipo 1
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| Descriptor Portuguese: | Displasia Ectodérmica Anidrótica Tipo 1 | ||||||
| Descriptor French: | Dysplasie ectodermique anhidrotique de type 1 | ||||||
| Entry term(s): |
Anhidrotic Ectodermal Dysplasia, X Linked Anhidrotic Ectodermal Dysplasia, X-Linked Anhydrotic Ectodermal Dysplasia, X Linked Anhydrotic Ectodermal Dysplasia, X-Linked CST Syndrome CST Syndromes Christ Siemens Touraine Syndrome Christ-Siemens-Touraine Syndrome Dysplasia 1, Ectodermal Ectodermal Dysplasia 1 Ectodermal Dysplasia 1, Anhydrotic Ectodermal Dysplasia 1s Ectodermal Dysplasia, Anhidrotic, X-Linked Ectodermal Dysplasia, Hypohidrotic, X-Linked Ectodermal Dysplasia, Hypohydridic, X-Linked Hypohidrotic Ectodermal Dysplasia Syndrome, CST Syndromes, CST X Linked Hypohydridic Ectodermal Dysplasia X-Linked Hypohydridic Ectodermal Dysplasia |
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| Tree number(s): |
C16.131.077.350.198 C16.131.831.350.198 C16.320.322.116 C16.320.850.250.198 C17.800.804.350.198 C17.800.827.250.198 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D053358 | ||||||
| Scope note: | An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN. |
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| 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 |
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| Public MeSH Note: | 2007; see ECTODERMAL DYSPLASIA 1993-2006 |
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| History Note: | 2007(1993) |
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| Related: |
Ectodysplasins
MeSH | ||||||
| DeCS ID: | 52139 | ||||||
| Unique ID: | D053358 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2007/01/01 | ||||||
| Date of Entry: | 2006/07/05 | ||||||
| Revision Date: | 2015/06/18 |
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Ectodermal Dysplasia 1, Anhidrotic
- Preferred
| Concept UI |
M0007033 |
| Scope note | An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN. |
| Preferred term | Ectodermal Dysplasia 1, Anhidrotic |
| Entry term(s) |
Anhidrotic Ectodermal Dysplasia, X Linked Anhidrotic Ectodermal Dysplasia, X-Linked Anhydrotic Ectodermal Dysplasia, X Linked Anhydrotic Ectodermal Dysplasia, X-Linked CST Syndrome CST Syndromes Christ Siemens Touraine Syndrome Christ-Siemens-Touraine Syndrome Dysplasia 1, Ectodermal Ectodermal Dysplasia 1 Ectodermal Dysplasia 1, Anhydrotic Ectodermal Dysplasia 1s Ectodermal Dysplasia, Anhidrotic, X-Linked Ectodermal Dysplasia, Hypohidrotic, X-Linked Ectodermal Dysplasia, Hypohydridic, X-Linked Hypohidrotic Ectodermal Dysplasia Syndrome, CST Syndromes, CST X Linked Hypohydridic Ectodermal Dysplasia X-Linked Hypohydridic Ectodermal Dysplasia |
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