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1 Possible Causes for Mutation in the LYRM7 Gene

  • Severe Infantile Carnitine Palmitoyl Transferase II Deficiency

    LYRM7 gene ( OMIM ) on chromosome 5q23; and MC3DN9 ( OMIM ), caused by mutation in the UQCC3 gene ( OMIM ) on chromosome 11q12.See also MTYCB ( OMIM ) for a discussion of[mendelian.co] […] in the CYC1 gene ( OMIM ) on chromosome 8q24; MC3DN7 ( OMIM ), caused by mutation in the UQCC2 gene ( OMIM ) on chromosome 6p21; MC3DN8 ( OMIM ), caused by mutation in the[mendelian.co] […] by mutation in the UQCRQ gene ( OMIM ) on chromosome 5q31; MC3DN5 ( OMIM ), caused by mutation in the UQCRC2 gene ( OMIM ) on chromosome 16p12; MC3DN6 ( OMIM ), caused by mutation[mendelian.co]

Further symptoms