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| Descriptor en español: |
Porfirias Hepáticas
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| Descriptor en inglés: | Porphyrias, Hepatic | ||||||
| Descriptor en portugués: | Porfirias Hepáticas | ||||||
| Descriptor en francés: | Porphyries hépatiques | ||||||
| Término(s) alternativo(s): |
Hepatic Porphyria Hepatic Porphyrias Porphyria, Hepatic |
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| Código(s) jeráquico(s): |
C06.552.830 C16.320.850.742 C17.800.827.742 C18.452.811.400 |
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| Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D017094 | ||||||
| Nota de alcance: | A group of metabolic diseases due to deficiency of one of a number of LIVER enzymes in the biosynthetic pathway of HEME. They are characterized by the accumulation and increased excretion of PORPHYRINS or its precursors. Clinical features include neurological symptoms (PORPHYRIA, ACUTE INTERMITTENT), cutaneous lesions due to photosensitivity (PORPHYRIA CUTANEA TARDA), or both (HEREDITARY COPROPORPHYRIA). Hepatic porphyrias can be hereditary or acquired as a result of toxicity to the hepatic tissues. |
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| Nota de indización: | do not confuse with PORPHYRIA, ERYTHROHEPATIC |
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| Calificadores permitidos: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital 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: |
Porphyria (1966-1992) |
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| Nota Pública de MeSH: | 2005; see PORPHYRIA, HEPATIC 1993-2004 |
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| Nota de historia: | 2005 (1993) |
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| Identificador de DeCS: | 30605 | ||||||
| ID del Descriptor: | D017094 | ||||||
| Documentos indizados en la Biblioteca Virtual de Salud (BVS): | Haga clic aquí para acceder a los documentos de la BVS | ||||||
| Fecha de establecimiento: | 01/01/1993 | ||||||
| Fecha de entrada: | 22/05/1992 | ||||||
| Fecha de revisión: | 05/06/2015 |
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Porphyrias, Hepatic
- Concepto preferido
| UI del concepto |
M0025973 |
| Nota de alcance | A group of metabolic diseases due to deficiency of one of a number of LIVER enzymes in the biosynthetic pathway of HEME. They are characterized by the accumulation and increased excretion of PORPHYRINS or its precursors. Clinical features include neurological symptoms (PORPHYRIA, ACUTE INTERMITTENT), cutaneous lesions due to photosensitivity (PORPHYRIA CUTANEA TARDA), or both (HEREDITARY COPROPORPHYRIA). Hepatic porphyrias can be hereditary or acquired as a result of toxicity to the hepatic tissues. |
| Término preferido | Porphyrias, Hepatic |
| Término(s) alternativo(s) |
Hepatic Porphyria Hepatic Porphyrias Porphyria, Hepatic |
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