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Results 1 - 10 of 43 for Familial arthropathy
  1. ... syndrome 6 MPV17-associated hepatocerebral MDS MTDPS6 Navajo familial neurogenic arthropathy Navajo neurohepatopathy Navajo neuropathy NNH Genetic Testing Registry: ...
  2. ... signs and symptoms.Another bone disorder, known as familial digital arthropathy-brachydactyly, has also been associated with mutations in ... CATION CHANNEL, SUBFAMILY V, MEMBER 4; TRPV4 DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL; FDAB PULMONARY DISEASE, CHRONIC OBSTRUCTIVE; COPD BRACHYOLMIA TYPE ...
  3. ... This predisposition can be passed through generations in families, but the inheritance pattern is unknown. Arthritis, degenerative Arthropathy Degenerative joint disease Degenerative polyarthritis Hypertrophic arthritis OA ...
  4. ... of affected individuals have at least one close family member with psoriasis or psoriatic arthritis. Arthropathic psoriasis Psoriatic arthropathy Genetic Testing Registry: Psoriatic arthritis, susceptibility to Psoriasis- ...
  5. ... Grewal D, Alcausin M, Rice GI, Crow YJ. Familial Aicardi-Goutieres syndrome due to SAMHD1 mutations is associated with chronic arthropathy and contractures. Am J Med Genet A. 2010 ...
  6. ... with no history of the disorder in their family. Rarely, an affected person inherits the mutation from one affected parent. LAPS syndrome Laryngotracheal stenosis, arthropathy, prognathism, and short stature Genetic Testing Registry: Myhre ...
  7. What Is Hemophilia? (Centers for Disease Control and Prevention)  
    Hemophilia/Start Here ... Hemophilia ... Centers for Disease Control and Prevention ... What is Hemophilia? Hemophilia is an inherited bleeding disorder in which the ...
  8. Osteoarthritis (National Library of Medicine)  
    ... joint that doesn't line up correctly. A family history of osteoarthritis. Some people inherit genetic changes ...
  9. ... a variant resembling Torg syndrome in a Saudi family. Am J Med Genet. 2000 Jul ... nodulosis, arthropathy and osteolysis (NAO) syndrome. Am J Med Genet. ...
  10. ... SA, Warman ML. Mutations in the CCN gene family member WISP3 cause progressive ... arthropathy of childhood (PPAC): a hereditary disorder simulating juvenile ...
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