- 1. Hutchinson Gilford syndrome
- [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. ( MSH )] (UMLS (CSP) C0033300) =Disease or Syndrome =Congenital Metabolic Disorder;
| - 2. hutterite
- [ ] (UMLS (CSP) C0598855) =Population Group ;
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