- Concept UI
- M0017668
- Scope Note
- 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 graying; 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.
- Terms
-
Progeria
Preferred Term
Term UI
T033535
Date01/01/1999
LexicalTag
NON
ThesaurusID
-
Hutchinson-Gilford Syndrome
Term UI
T033534
Date01/01/1975
LexicalTag
EPO
ThesaurusID
-
Hutchinson Gilford Progeria Syndrome
Term UI
T834214
Date12/12/2012
LexicalTag
NON
ThesaurusID
ORD (2010)
-
Hutchinson-Gilford Progeria Syndrome
Term UI
T811837
Date11/15/2011
LexicalTag
NON
ThesaurusID