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| Descriptor en español: |
Seudoxantoma Elástico
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| Descriptor en inglés: | Pseudoxanthoma Elasticum | ||||||
| Descriptor en portugués: | Pseudoxantoma Elástico | ||||||
| Descriptor en francés: | Pseudoxanthome élastique | ||||||
| Término(s) alternativo(s): |
Elasticum, Incomplete Pseudoxanthoma Elasticums, Incomplete Pseudoxanthoma Groenblad-Strandberg Syndrome Gronblad Strandberg Syndrome Gronblad-Strandberg Syndrome Incomplete Pseudoxanthoma Elasticum Incomplete Pseudoxanthoma Elasticums Pseudoxanthoma Elasticum, Autosomal Dominant Pseudoxanthoma Elasticum, Forme Fruste Pseudoxanthoma Elasticum, Incomplete Pseudoxanthoma Elasticums, Incomplete Syndrome, Gronblad-Strandberg |
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| Código(s) jeráquico(s): |
C14.907.454.530 C15.378.463.515.530 C16.131.831.766 C16.320.850.750 C17.300.766 C17.800.804.766 C17.800.827.750 |
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| Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D011561 | ||||||
| Nota de alcance: | An inherited disorder of connective tissue with extensive degeneration and calcification of ELASTIC TISSUE primarily in the skin, eye, and vasculature. At least two forms exist, autosomal recessive and autosomal dominant. This disorder is caused by mutations of one of the ATP-BINDING CASSETTE TRANSPORTERS. Patients are predisposed to MYOCARDIAL INFARCTION and GASTROINTESTINAL HEMORRHAGE. |
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| Nota de indización: | in titles & translations use diacritic: Grönblad |
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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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| Identificador de DeCS: | 11998 | ||||||
| ID del Descriptor: | D011561 | ||||||
| Clasificación de la NLM: | WD 375 | ||||||
| Documentos indizados en la Biblioteca Virtual de Salud (BVS): | Haga clic aquí para acceder a los documentos de la BVS | ||||||
| Fecha de establecimiento: | 01/01/1966 | ||||||
| Fecha de entrada: | 01/01/1999 | ||||||
| Fecha de revisión: | 18/06/2015 |
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Pseudoxanthoma Elasticum
- Concepto preferido
Gronblad-Strandberg Syndrome
- Más estrecho
Pseudoxanthoma Elasticum, Incomplete
- Más estrecho
| UI del concepto |
M0017968 |
| Nota de alcance | An inherited disorder of connective tissue with extensive degeneration and calcification of ELASTIC TISSUE primarily in the skin, eye, and vasculature. At least two forms exist, autosomal recessive and autosomal dominant. This disorder is caused by mutations of one of the ATP-BINDING CASSETTE TRANSPORTERS. Patients are predisposed to MYOCARDIAL INFARCTION and GASTROINTESTINAL HEMORRHAGE. |
| Término preferido | Pseudoxanthoma Elasticum |
| UI del concepto |
M0017969 |
| Término preferido | Gronblad-Strandberg Syndrome |
| Término(s) alternativo(s) |
Groenblad-Strandberg Syndrome Gronblad Strandberg Syndrome Syndrome, Gronblad-Strandberg |
| UI del concepto |
M0501068 |
| Término preferido | Pseudoxanthoma Elasticum, Incomplete |
| Término(s) alternativo(s) |
Elasticum, Incomplete Pseudoxanthoma Elasticums, Incomplete Pseudoxanthoma Incomplete Pseudoxanthoma Elasticum Incomplete Pseudoxanthoma Elasticums Pseudoxanthoma Elasticum, Autosomal Dominant Pseudoxanthoma Elasticum, Forme Fruste Pseudoxanthoma Elasticums, Incomplete |
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