0 Chromosome 19

  • Myotonia dystrophica
  • Insulin receptor gene
  • NPHS 1 (Nephrin) - Congenital FINNISH type of Nephrotic Syndrome (AR)

Note :
NPHS 1 - Chromosome 19
NPHS 2 - Chromosome 1

Human Insulin gene - Chromosome 11
Insulin Receptor gene - Chromosome 19

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