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Results 1 - 10 of 10 for Calcinosis
  1. Hyperphosphatemic familial tumoral calcinosis 
    Hyperphosphatemic familial tumoral calcinosis (HFTC) is a condition characterized by an increase in the levels of phosphate in the blood (hyperphosphatemia) and abnormal ...
    https://medlineplus.gov/...rphosphatemic-familial-tumoral-calcinosis - Genetics
  2. Primary familial brain calcification 
    ... signs and symptoms of the condition. Bilateral striopallidodentate calcinosis Cerebrovascular ferrocalcinosis Familial idiopathic basal ganglia calcification FIBGC ...
    https://medlineplus.gov/.../primary-familial-brain-calcification - Genetics
  3. GALNT3 gene 
    ... have been found to cause hyperphosphatemic familial tumoral calcinosis (HFTC), a condition characterized by an increase in ... hyperphosphatemia) and abnormal deposits of phosphate and calcium (calcinosis) in the body's tissues. GALNT3 gene mutations ...
    https://medlineplus.gov/genetics/gene/galnt3 - Genetics
  4. KL gene 
    ... has been found to cause hyperphosphatemic familial tumoral calcinosis (HFTC), a condition characterized by an increase in ... hyperphosphatemia) and abnormal deposits of phosphate and calcium (calcinosis) in the body's tissues. The KL gene ...
    https://medlineplus.gov/genetics/gene/kl - Genetics
  5. FGF23 gene 
    ... have been found to cause hyperphosphatemic familial tumoral calcinosis (HFTC), a condition characterized by an increase in ... hyperphosphatemia) and abnormal deposits of phosphate and calcium (calcinosis) in the body's tissues. Mutations in the ...
    https://medlineplus.gov/genetics/gene/fgf23 - Genetics
  6. Systemic scleroderma 
    ... on their fingers, painful bumps under the skin (calcinosis), or small clusters of enlarged blood vessels just ... named for the common features of the condition: calcinosis, Raynaud phenomenon, esophageal motility dysfunction, sclerodactyly, and telangiectasia. ...
    https://medlineplus.gov/genetics/condition/systemic-scleroderma - Genetics
  7. Systemic lupus erythematosus 
    ... in SLE include calcium deposits under the skin (calcinosis), damaged blood vessels (vasculitis) in the skin, and ...
    https://medlineplus.gov/.../condition/systemic-lupus-erythematosus - Genetics
  8. Poikiloderma with neutropenia 
    ... palmoplantar keratoderma); calcium deposits that form small nodules (calcinosis cutis), especially on the knees, elbows, or ears; ...
    https://medlineplus.gov/.../condition/poikiloderma-with-neutropenia - Genetics
  9. Hartsfield syndrome 
    ... heterozygous missense mutation in FGFR1 and incorporating tumoral calcinosis. Am J Med Genet A. 2016 Aug;170( ...
    https://medlineplus.gov/genetics/condition/hartsfield-syndrome - Genetics
  10. Idiopathic inflammatory myopathy 
    ... deposits form hard, painful bumps under the skin (calcinosis).In sporadic inclusion body myositis, the muscles most ...
    https://medlineplus.gov/.../idiopathic-inflammatory-myopathy - Genetics