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Det sätt begreppsrelationer visas:
Progeria
Hierarki: | ∟ ∟ ∟ ∟ Progeria 15 sidobegrepp∟ ∟ ∟ ∟ Progeria 15 sidobegreppX |
Bredare villkor: | |
Anmärkning: | An abnormal congenital condition, associated with defects in the LAMIN TYPE A gene, which is characterized by premature aging in children, where all the changes of cell senescence occur. It is manifested by premature greying; hair loss; hearing loss (DEAFNESS); cataracts (CATARACT); ARTHRITIS; OSTEOPOROSIS; DIABETES MELLITUS; atrophy of subcutaneous fat; skeletal hypoplasia; elevated urinary HYALURONIC ACID; and accelerated ATHEROSCLEROSIS. Many affected individuals develop malignant tumors, especially SARCOMA.
X |
activeMeSHYear*: | 2007X |
dateCreated*: | 1999-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | NLMX |
Relaterad term: | |
Typ: | |
Samordna villkor: | |
URI: | |
Termer och motsvarande begrepp: | Hutchinson-Gilfordin syndrooma (fi, ersatt) XHutchinson-Gilfordin oireyhtymä (fi, ersatt) Ennenaikainen vanheneminen (fi, ersatt) Hutchinson-Gilford Syndrome (en, ersatt) Progeria (la-FI, ersatt) Syndroma Hutchinson-Gilfordin (la-FI, ersatt) |
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