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Results 1 - 10 of 25 for Family history
  1. CDH1 gene 
    ... in lobular breast cancers in women without a family history of the disease. These genetic changes, known as ... of BCD syndrome and with or without a family history of HDGC (both described above). The CDH1 gene ...
    https://medlineplus.gov/genetics/gene/cdh1 - Genetics
  2. CACNA1A gene 
    ... sporadic hemiplegic migraine occurs in people with no family history of the condition. As in FHM1, sporadic hemiplegic migraine caused by CACNA1A gene variants is commonly associated with migraines ... also found in families with FHM1. The altered channels are more active ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics
  3. BRCA1 gene 
    ... BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies. Am J ...
    https://medlineplus.gov/genetics/gene/brca1 - Genetics
  4. APC gene 
    ... patients with apparently sporadic desmoid tumors but a family history of colorectal carcinoma. Dis Colon Rectum. 2005 Jun; ...
    https://medlineplus.gov/genetics/gene/apc - Genetics
  5. LRRK2 gene 
    ... s disease cases, in which there is no family history of the disease.Studies in Chinese and Japanese ...
    https://medlineplus.gov/genetics/gene/lrrk2 - Genetics
  6. PTEN gene 
    ... in some breast cancers in women without a family history of the disease. Somatic mutations are not inherited ...
    https://medlineplus.gov/genetics/gene/pten - Genetics
  7. BAP1 gene 
    ... cases, the cancers occur in people with no family history of the cancer and are considered sporadic. Affected ...
    https://medlineplus.gov/genetics/gene/bap1 - Genetics
  8. ATP1A2 gene 
    ... sporadic hemiplegic migraine occurs in people with no family history of the condition. As in FHM2, most of ...
    https://medlineplus.gov/genetics/gene/atp1a2 - Genetics
  9. CARD14 gene 
    ... increased risk of psoriasis in people without a family history of the disorder. Studies suggest that these genetic ...
    https://medlineplus.gov/genetics/gene/card14 - Genetics
  10. KIF1B gene 
    ... inherited KIF1B gene mutations have been identified in families with a history of neuroblastoma. These mutations change single protein building blocks (amino acids) in the kinesin family member 1B protein. Studies suggest that deletion or ...
    https://medlineplus.gov/genetics/gene/kif1b - Genetics
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