- 1. Sjogren Larsson syndrome
- [An autosomal recessive neurocutaneous disorder characterized by severe ichthyosis MENTAL RETARDATION; SPASTIC PARAPLEGIA; and congenital ICHTHYOSIS. It is caused by mutation of gene encoding microsomal fatty ALDEHYDE DEHYDROGENASE leading to defect in fatty alcohol metabolism. ( MSH )] (UMLS (CSP) C0037231) =Congenital Abnormality; Disease or Syndrome =Ichthyosis;
inborn lipid storage disorder | - 2. Sjogren's syndrome
- [symptom complex of unknown etiology, usually occurring in middle-aged or older women, marked by the triad of keratoconjunctivitis sicca with or without lacrimal gland enlargement, xerostomia with or without salivary gland enlargement, and the presence of a connective tissue disease, usually rheumatoid arthritis but sometimes systemic lupus erythematosus, scleroderma, or polymyositis; an abnormal immune response has been implicated. ( CSP )] (UMLS (CSP) C1527336) Syndrome, sjogren's;
=Disease or Syndrome ;
=Arthritis, Rheumatoid;
autoimmune disease;
Collagen Diseases;
Dry Eye Syndrome;
KCS;
syndrome;
aptyalism;
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