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84 results
  1. xmlghr-summaries.xml 
    https://medlineplus.gov/download/ghr-summaries.xml
    ... published></gene-summary><gene-summary ><gene-symbol >FANCC</gene-symbol><name >FA complementation group C</name><ghr-page >https://medlineplus.gov/genetics/gene/ ...
  2. xmlTopicIndex.xml 
    https://medlineplus.gov/download/TopicIndex.xml
    ... gene/fanca</url></topic><topic ><title >FANCC: FA complementation group C</title><url >https://medlineplus.gov/genetics/gene/fancc</url></topic><topic ><title >FANCG: FA complementation ...
  3. Fanconi Anemia - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1401
    ... IN CHINESE HAMSTER, 2; XRCC2 600901 FANCONI ANEMIA, COMPLEMENTATION GROUP E; FANCE 602774 RAD51 PARALOG C; RAD51C 602956 FANCG GENE; FANCG 603467 FANCONI ANEMIA, COMPLEMENTATION GROUP F; FANCF ...
  4. FANCC gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/fancc
    ... About This Health Condition Other Names for This Gene FAC FACC FANCC_HUMAN Fanconi anemia complementation group C Fanconi anemia, complementation group C Additional Information & Resources ...
  5. XPC gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/xpc
    ... About This Health Condition Other Names for This Gene RAD4 Xeroderma pigmentosum group C-complementing protein xeroderma pigmentosum, complementation group C XP3 XPC_HUMAN XPCC Additional Information & ...
  6. Molybdenum cofactor deficiency: MedlinePlus Genetics 
    https://medlineplus.gov/.../condition/molybdenum-cofactor-deficiency
    ... disorder, named types A, B, and C (or complementation groups A, B, and C). The forms have the same signs and symptoms but are distinguished by their genetic cause: MOCS1 gene mutations cause type A, MOCS2 gene mutations cause ...
  7. Zellweger Spectrum Disorder - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1448
    ... the total number of individuals belonging to this complementation group who underwent sequencing of that gene . 10. One PEX6 variant, c.2578C>T (p.Arg860Trp), has been associated with ...
  8. Isolated Methylmalonic Acidemia - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1231
    ... T, Leclerc D, Wilson A, Wu X, Dore C, Hudson T, Rosenblatt DS, Gravel RA. Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on ...
  9. GPHN gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/gphn
    ... form of the disorder designated type C or complementation group C. This is the rarest form of the condition, affecting only a small number of individuals. The GPHN gene mutations involved in molybdenum cofactor deficiency likely reduce ...
  10. Xeroderma pigmentosum: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/condition/xeroderma-pigmentosum
    ... Disorders (NORD) Clinical Trials ClinicalTrials.gov Catalog of Genes and Diseases from OMIM XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD XERODERMA ...
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