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Results 1 - 10 of 13 for Familial arthropathy
  1. MPV17-related hepatocerebral mitochondrial DNA depletion syndrome 
    ... syndrome 6 MPV17-associated hepatocerebral MDS MTDPS6 Navajo familial neurogenic arthropathy Navajo neurohepatopathy Navajo neuropathy NNH Genetic Testing Registry: ...
    https://medlineplus.gov/...bral-mitochondrial-dna-depletion-syndrome - Genetics
  2. TRPV4 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/trpv4 - Genetics
  3. Osteoarthritis 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/osteoarthritis - Genetics
  4. Psoriatic arthritis 
    ... 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- ...
    https://medlineplus.gov/genetics/condition/psoriatic-arthritis - Genetics
  5. SAMHD1 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/samhd1 - Genetics
  6. Myhre syndrome 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/myhre-syndrome - Genetics
  7. Multicentric osteolysis, nodulosis, and arthropathy 
    ... 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. ...
    https://medlineplus.gov/...tric-osteolysis-nodulosis-and-arthropathy - Genetics
  8. Progressive pseudorheumatoid dysplasia 
    ... SA, Warman ML. Mutations in the CCN gene family member WISP3 cause progressive ... arthropathy of childhood (PPAC): a hereditary disorder simulating juvenile ...
    https://medlineplus.gov/.../progressive-pseudorheumatoid-dysplasia - Genetics
  9. MMP2 gene 
    ... been found to cause multicentric osteolysis, nodulosis, and arthropathy (MONA), a rare inherited bone disease that is ... and feet, and related joint problems described as arthropathy. Each of the known MMP2 gene mutations eliminates ...
    https://medlineplus.gov/genetics/gene/mmp2 - Genetics
  10. Tumor necrosis factor receptor-associated periodic syndrome 
    ... pathogenesis, treatment, and place relative to other periodic joint diseases. Joint Bone Spine. 2004 Jul;71(4):284- ... LJ. Autosomal recessive transmission of TRAPS in a family with a novel TNFRSF1A mutation. Scand J Rheumatol. ...
    https://medlineplus.gov/...tor-receptor-associated-periodic-syndrome - Genetics
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