| AFS | acquired or adult Fanconi syndrome; alternative financing system; American Fertility Society; antifi... |
|---|---|
| FA | false aneurysm; Families Anonymous; Fanconi anemia; far advanced; fatty acid; febrile antigen; femor... |
| FACA | Fanconi anemia complementation group A; Fellow of the American College of Anesthetists; Fellow of th... |
| FACB | Fanconi anemia complementation group B |
| FACC | Fanconi anemia complementation group C; Fellow of the American College of Cardiologists |
| FA | Fanconi Anemia |
|---|---|
| FS | Fanconi syndrome |
| Fanconi syndrome | <syndrome> Transport disease (recessive defect) in which the renal reabsorption of several substances (phosphate, glucose, amino acids) is impaired. (18 Nov 1997) |
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| Fanconi's anaemia | <haematology> A rare inherited type of aplastic anaemia which carries an increased risk to the patient of developing leukaemia. May be treated by bone marrow transplant. Origin: Gr. Haima = blood (13 Nov 1997) |
| Fanconi's pancytopenia | fanconi's anaemia |
| Fanconi's syndrome | <syndrome> A group of conditions with characteristic disorders of renal tubular function, which may be classified as: 1. Cystinosis, an autosomal recessive disease of early childhood. 2. Adult Fanconi syndrome, a rare hereditary form, probably due to a recessive gene different from that found in cystinosis, characterised by the tubular malfunction seen in cystinosis and by osteomalacia, but without cystine deposit in tissues. 3. Acquired Fanconi syndrome, which may be associated with multiple myeloma or may result from chemical poisoning, injury, or persisting damage of proximal tubular epithelium due to various causes, leading to multiple defects of tubular function. (05 Mar 2000) |
| Fanconi, Guido | <person> Swiss paediatrician, 1892-1979. See: Fanconi's anaemia, Fanconi's pancytopenia, Fanconi's syndrome, De Toni-Fanconi syndrome, Lignac-Fanconi syndrome. (05 Mar 2000) |
| pancytopenia, fanconi | A genetic (inherited) disease with progressive decline in blood cells and a tendency to leukaemia. Also known as fanconi anaemia. (12 Dec 1998) |
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| De Toni-Fanconi syndrome | Lysosomal storage disorders of unknown molecular defect, characterised by widespread deposition of cystine crystals in reticuloendothelial cells. (12 Dec 1998) |
| Lignac-Fanconi syndrome | Lysosomal storage disorders of unknown molecular defect, characterised by widespread deposition of cystine crystals in reticuloendothelial cells. (12 Dec 1998) |
Synonyms : Fanconi's Anemia, Anemia, Fanconi's, Anemias, Fanconi, Fanconi Anemias
Synonyms : FANCA Protein, Fanconi Anemia Group A Complementing Protein, Fanconi Anemia Group A Protein
Synonyms : FANCC Protein, Fanconi Anemia Group C Complementing Protein, Fanconi Anemia Group C Protein
Synonyms : FANCD2 Protein, Fanconi Anemia Group D2 Complementing Protein, Fanconi Anemia Group D2 Protein
Synonyms : FANCE Protein, Fanconi Anemia Group E Complementing Protein, Fanconi Anemia Group E Protein
| Fanconi's anemia |
a rare congenital anemia characterized by pancytopenia and hypoplasia of the bone marrow
출처: wordnet.princeton.edu/perl/webwn
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| Fanconi's anemia |
A rare and often fatal inherited disease in which the bone marrow fails to produce red blood cells, white blood cells, platelets, or a combination of these cells. The disease may transform into myelodysplastic syndrome or leukemia. Also called Fanconi's syndrome.
출처: www.stjude.org/glossary
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| Fanconi's syndrome |
A rare and often fatal inherited disease in which the bone marrow fails to produce red blood cells, white blood cells, platelets, or a combination of these cells. The disease may transform into myelodysplastic syndrome or leukemia. Also called Fanconi anemia.
출처: www.stjude.org/glossary
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| Fanconi's anemia |
An heritable disease in human beings with a syndrome of congenital malformations (decreased blood cells, short stature, patchy dark skin pimentation, predisposition to cancer especially leukaemia) inherited as an autosomal recessive.
출처: helios.bto.ed.ac.uk/bto/glossary/ef.htm
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| Fanconi s. |
1. a rare recessive disorder with a poor prognosis, characterized by pancytopenia, bone marrow hypoplasia, and patchy brown skin discoloration due to deposition of melanin, as well as multiple congenital anomalies of the musculoskeletal and genitourinary systems. Called also Fanconi's anemia, pancytopenia, or panmyelopathy; congenital hypoplastic anemia; congenital pancytopenia; constitutional infantile panmyelopathy; and pancytopenia-dysmelia s. 2. a general term for a group of diseases marked by dysfunction of the proximal renal tubules (see proximal renal tubular acidosis, under acidosis) with generalized hyperaminoaciduria, renal glycosuria, hyperphosphaturia, and bicarbonate and water loss. The most common cause is cystinosis (q.v.), but it is also associated with other genetic diseases and occurs in idiopathic and acquired forms. When unassociated with cystinosis, the disorder is also called de Toni-Fanconi syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Fanconi | a rare congenital anemia characterized by pancytopenia and hypoplasia of the bone marrow |
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| Fanconi | a rare congenital anemia characterized by pancytopenia and hypoplasia of the bone marrow |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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