| Descriptor English: | Epidermolysis Bullosa Dystrophica | ||||||
| Descriptor Spanish: |
Epidermólisis Ampollosa Distrófica
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| Descriptor Portuguese: | Epidermólise Bolhosa Distrófica | ||||||
| Descriptor French: | Épidermolyse bulleuse dystrophique | ||||||
| Entry term(s): |
Bullosa Dystrophica, Epidermolysis Bullosa Dystrophicas, Epidermolysis Bullosa, Dystrophic Epidermolysis Bullosas, Dystrophic Epidermolysis Cockayne Touraine Disease Cockayne Touraine Type Epidermolysis Bullosa Cockayne-Touraine Disease Cockayne-Touraine Type Epidermolysis Bullosa Dystrophic Epidermolysis Bullosa Dystrophic Epidermolysis Bullosa, Autosomal Recessive Dystrophic Epidermolysis Bullosas Dystrophica, Epidermolysis Bullosa Dystrophicas, Epidermolysis Bullosa Epidermolysis Bullosa Dystrophica, Autosomal Recessive Epidermolysis Bullosa Dystrophica, Cockayne Touraine Type Epidermolysis Bullosa Dystrophica, Cockayne-Touraine Type Epidermolysis Bullosa Dystrophica, Dominant Epidermolysis Bullosa Dystrophica, Hallopeau Siemens Type Epidermolysis Bullosa Dystrophica, Hallopeau-Siemens Type Epidermolysis Bullosa Dystrophica, Recessive Epidermolysis Bullosa Dystrophicas Epidermolysis Bullosa, Dystrophic Epidermolysis Bullosas, Dystrophic Hallopeau Siemens Disease Hallopeau-Siemens Disease |
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| Tree number(s): |
C16.131.831.493.160 C16.320.850.275.160 C17.300.200.367 C17.800.804.493.160 C17.800.827.275.160 C17.800.865.410.160 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D016108 | ||||||
| Scope note: | Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in COLLAGEN TYPE VII, a major component fibrils of BASEMENT MEMBRANE and EPIDERMIS. |
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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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| Previous Indexing: |
Epidermolysis Bullosa (1966-1990) |
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| Public MeSH Note: | 1991 |
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| History Note: | 1991 |
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| DeCS ID: | 28925 | ||||||
| Unique ID: | D016108 | ||||||
| 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 |
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Epidermolysis Bullosa Dystrophica
- Preferred
Hallopeau-Siemens Disease
- Narrower
Cockayne-Touraine Disease
- Narrower
| Concept UI |
M0024601 |
| Scope note | Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in COLLAGEN TYPE VII, a major component fibrils of BASEMENT MEMBRANE and EPIDERMIS. |
| Preferred term | Epidermolysis Bullosa Dystrophica |
| Entry term(s) |
Bullosa Dystrophica, Epidermolysis Bullosa Dystrophicas, Epidermolysis Bullosa, Dystrophic Epidermolysis Bullosas, Dystrophic Epidermolysis Dystrophic Epidermolysis Bullosa Dystrophic Epidermolysis Bullosas Dystrophica, Epidermolysis Bullosa Dystrophicas, Epidermolysis Bullosa Epidermolysis Bullosa Dystrophicas Epidermolysis Bullosa, Dystrophic Epidermolysis Bullosas, Dystrophic |
| Concept UI |
M0024602 |
| Preferred term | Hallopeau-Siemens Disease |
| Entry term(s) |
Dystrophic Epidermolysis Bullosa, Autosomal Recessive Epidermolysis Bullosa Dystrophica, Autosomal Recessive Epidermolysis Bullosa Dystrophica, Hallopeau Siemens Type Epidermolysis Bullosa Dystrophica, Hallopeau-Siemens Type Epidermolysis Bullosa Dystrophica, Recessive Hallopeau Siemens Disease |
| Concept UI |
M0024600 |
| Preferred term | Cockayne-Touraine Disease |
| Entry term(s) |
Cockayne Touraine Disease Cockayne Touraine Type Epidermolysis Bullosa Cockayne-Touraine Type Epidermolysis Bullosa Epidermolysis Bullosa Dystrophica, Cockayne Touraine Type Epidermolysis Bullosa Dystrophica, Cockayne-Touraine Type Epidermolysis Bullosa Dystrophica, Dominant |
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