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| Descriptor en español: |
Eritroqueratodermia Variable
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| Descriptor en inglés: | Erythrokeratodermia Variabilis | ||||||
| Descriptor en portugués: | Eritroceratodermia Variável | ||||||
| Descriptor en francés: | Érythrokératodermie variabilis | ||||||
| Término(s) alternativo(s): |
Erythro et Keratodermia Variabilis Erythrokeratodermia Figurata Variabilis Erythrokeratodermia Figurata, Congenital Familial, in Plaques Erythrokeratodermia Variabilis with Erythema Gyratum Repens Erythrokeratodermia, Progressive Symmetric Greither Disease Mendes De Costa Syndrome Progressive Symmetric Erythrokeratodermia Transgrediens et Progrediens Palmoplantar Keratoderma |
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| Código(s) jeráquico(s): |
C16.320.850.337 C17.800.229.606 C17.800.428.304 C17.800.827.337 |
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| Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D056266 | ||||||
| Nota de alcance: | An autosomal dominant skin disease characterized by transient and variable noninflammatory ERYTHEMA and hyperkeratosis. It has been associated with mutations in the genes that code for CONNEXINS. Erythrokeratodermia variabilis inherited in an autosomal recessive fashion has also been reported. Affected individuals often develop PALMOPLANTAR KERATODERMA. |
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| Calificadores permitidos: |
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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| Indexación anterior: |
Erythema (1998-2009) Keratosis (2002-2009) Skin Diseases, Genetic (2002-2009) |
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| Nota Pública de MeSH: | 2010; ERYTHROKERATODERMIA FIGURATA, CONGENITAL FAMILIAL, IN PLAQUES and ERYTHROKERATODERMIA VARIABILIS WITH ERYTHEMA GYRATUM REPENS were indexed under PAPILLON-LEFEVRE DISEASE 2010-2016. |
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| Nota de historia: | 2010 |
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| Vea también los descriptores: |
Connexins
MeSH Keratoderma, Palmoplantar MeSH | ||||||
| Identificador de DeCS: | 53558 | ||||||
| ID del Descriptor: | D056266 | ||||||
| Documentos indizados en la Biblioteca Virtual de Salud (BVS): | Haga clic aquí para acceder a los documentos de la BVS | ||||||
| Fecha de establecimiento: | 01/01/2010 | ||||||
| Fecha de entrada: | 06/07/2009 | ||||||
| Fecha de revisión: | 20/06/2017 |
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Erythrokeratodermia Variabilis
- Concepto preferido
Greither Disease
- Relacionado pero no más amplio ni más estrecho
| UI del concepto |
M0526847 |
| Nota de alcance | An autosomal dominant skin disease characterized by transient and variable noninflammatory ERYTHEMA and hyperkeratosis. It has been associated with mutations in the genes that code for CONNEXINS. Erythrokeratodermia variabilis inherited in an autosomal recessive fashion has also been reported. Affected individuals often develop PALMOPLANTAR KERATODERMA. |
| Término preferido | Erythrokeratodermia Variabilis |
| Término(s) alternativo(s) |
Erythro et Keratodermia Variabilis Erythrokeratodermia Figurata Variabilis Erythrokeratodermia Figurata, Congenital Familial, in Plaques Erythrokeratodermia Variabilis with Erythema Gyratum Repens Erythrokeratodermia, Progressive Symmetric Mendes De Costa Syndrome Progressive Symmetric Erythrokeratodermia |
| UI del concepto |
M0527605 |
| Término preferido | Greither Disease |
| Término(s) alternativo(s) |
Transgrediens et Progrediens Palmoplantar Keratoderma |
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