Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 2273
  • Symbol: FHL1
  • Description: four and a half LIM domains 1

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Disease_Term Source Rank Other Values
Reducing body myopathy, X-linked 1b, with late childhood or adult onset, 300718 (3) OMIM high
  • Genome region : Xq26.3
  • OMIM_ID : 300163 OMIM gene ID
  • OMIM_ID : 300718 OMIM phenotype ID
Emery-Dreifuss muscular dystrophy 6, X-linked, 300696 (3) OMIM high
  • Genome region : Xq26.3
  • OMIM_ID : 300163 OMIM gene ID
  • OMIM_ID : 300696 OMIM phenotype ID
Scapuloperoneal myopathy, X-linked dominant, 300695 (3) OMIM high
  • Genome region : Xq26.3
  • OMIM_ID : 300163 OMIM gene ID
  • OMIM_ID : 300695 OMIM phenotype ID
Myopathy, X-linked, with postural muscle atrophy, 300696 (3) OMIM high
  • Genome region : Xq26.3
  • OMIM_ID : 300163 OMIM gene ID
  • OMIM_ID : 300696 OMIM phenotype ID
Reducing body myopathy, X-linked 1a, severe, infantile or early childhood onset, 300717 (3) OMIM high
  • Genome region : Xq26.3
  • OMIM_ID : 300163 OMIM gene ID
  • OMIM_ID : 300717 OMIM phenotype ID