Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:1674
  • Symbol:DES
  • Description:desmin

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Disease_Term Source Rank Other Values
Myopathy, myofibrillar, 1, 601419 (3) OMIM high
  • Genome region :2q35
  • OMIM_ID :125660OMIM gene ID
  • OMIM_ID :601419OMIM phenotype ID
Scapuloperoneal syndrome, neurogenic, Kaeser type, 181400 (3) OMIM high
  • Genome region :2q35
  • OMIM_ID :125660OMIM gene ID
  • OMIM_ID :181400OMIM phenotype ID
Cardiomyopathy, dilated, 1I, 604765 (3) OMIM high
  • Genome region :2q35
  • OMIM_ID :125660OMIM gene ID
  • OMIM_ID :604765OMIM phenotype ID
?Muscular dystrophy, limb-girdle, type 2R, 615325 (3) OMIM high
  • Genome region :2q35
  • OMIM_ID :125660OMIM gene ID
  • OMIM_ID :615325OMIM phenotype ID