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| Descriptor en español: |
Síndrome de la Uña-Rótula
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| Descriptor en inglés: | Nail-Patella Syndrome | ||||||
| Descriptor en portugués: | Síndrome da Unha-Patela | ||||||
| Descriptor en francés: | Syndrome nail-patella | ||||||
| Término(s) alternativo(s): |
Disease, Fong Fong Disease Hereditary Onycho-Osteodysplasia Hereditary Osteo-Onychodysplasia Hereditary Osteo-Onychodysplasias Nail Patella Syndrome Onychoosteodysplasia Osteo Onychodysplasia, Hereditary Osteo-Onychodysplasia, Hereditary Osteo-Onychodysplasias, Hereditary Osterreicher Syndrome Pelvic Horn Syndrome Syndrome, Nail-Patella Syndrome, Osterreicher Syndrome, Pelvic Horn Syndrome, Turner-Kieser Turner Kieser Syndrome Turner-Kieser Syndrome |
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| Código(s) jeráquico(s): |
C05.550.629 C16.131.077.606 C16.320.600 C17.800.529.400 |
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| Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D009261 | ||||||
| Nota de alcance: | A syndrome of multiple abnormalities characterized by the absence or hypoplasia of the PATELLA and congenital nail dystrophy. It is a genetically determined autosomal dominant trait. |
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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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| Nota Pública de MeSH: | 65 |
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| Nota de historia: | 65(63) |
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| Identificador de DeCS: | 9452 | ||||||
| ID del Descriptor: | D009261 | ||||||
| Documentos indizados en la Biblioteca Virtual de Salud (BVS): | Haga clic aquí para acceder a los documentos de la BVS | ||||||
| Fecha de establecimiento: | 01/01/1965 | ||||||
| Fecha de entrada: | 01/01/1999 | ||||||
| Fecha de revisión: | 08/07/2013 |
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Nail-Patella Syndrome
- Concepto preferido
| UI del concepto |
M0014428 |
| Nota de alcance | A syndrome of multiple abnormalities characterized by the absence or hypoplasia of the PATELLA and congenital nail dystrophy. It is a genetically determined autosomal dominant trait. |
| Término preferido | Nail-Patella Syndrome |
| Término(s) alternativo(s) |
Disease, Fong Fong Disease Hereditary Onycho-Osteodysplasia Hereditary Osteo-Onychodysplasia Hereditary Osteo-Onychodysplasias Nail Patella Syndrome Onychoosteodysplasia Osteo Onychodysplasia, Hereditary Osteo-Onychodysplasia, Hereditary Osteo-Onychodysplasias, Hereditary Osterreicher Syndrome Pelvic Horn Syndrome Syndrome, Nail-Patella Syndrome, Osterreicher Syndrome, Pelvic Horn Syndrome, Turner-Kieser Turner Kieser Syndrome Turner-Kieser Syndrome |
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