| Descriptor English: | Erythrokeratodermia Variabilis | ||||||
| Descriptor Spanish: |
Eritroqueratodermia Variable
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| Descriptor Portuguese: | Eritroceratodermia Variável | ||||||
| Descriptor French: | Érythrokératodermie variabilis | ||||||
| Entry term(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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| Tree number(s): |
C16.320.850.337 C17.800.229.606 C17.800.428.304 C17.800.827.337 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D056266 | ||||||
| Scope note: | 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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| 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: |
Erythema (1998-2009) Keratosis (2002-2009) Skin Diseases, Genetic (2002-2009) |
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| Public MeSH Note: | 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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| History Note: | 2010 |
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| Related: |
Connexins
MeSH Keratoderma, Palmoplantar MeSH | ||||||
| DeCS ID: | 53558 | ||||||
| Unique ID: | D056266 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2010/01/01 | ||||||
| Date of Entry: | 2009/07/06 | ||||||
| Revision Date: | 2017/06/20 |
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Erythrokeratodermia Variabilis
- Preferred
Greither Disease
- Related but not broader or narrower
| Concept UI |
M0526847 |
| Scope note | 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. |
| Preferred term | Erythrokeratodermia Variabilis |
| Entry term(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 |
| Concept UI |
M0527605 |
| Preferred term | Greither Disease |
| Entry term(s) |
Transgrediens et Progrediens Palmoplantar Keratoderma |
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