Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:170302
  • Symbol:ARX
  • Description:aristaless related homeobox

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Disease_Term Source Rank Other Values
Mental retardation, X-linked 29 and others, 300419 (3) OMIM high
  • Genome region :Xp21.3
  • OMIM_ID :300382OMIM gene ID
  • OMIM_ID :300419OMIM phenotype ID
Epileptic encephalopathy, early infantile, 1, 308350 (3) OMIM high
  • Genome region :Xp21.3
  • OMIM_ID :300382OMIM gene ID
  • OMIM_ID :308350OMIM phenotype ID
Partington syndrome, 309510 (3) OMIM high
  • Genome region :Xp21.3
  • OMIM_ID :300382OMIM gene ID
  • OMIM_ID :309510OMIM phenotype ID
Hydranencephaly with abnormal genitalia, 300215 (3) OMIM high
  • Genome region :Xp21.3
  • OMIM_ID :300215OMIM phenotype ID
  • OMIM_ID :300382OMIM gene ID
Proud syndrome, 300004 (3) OMIM high
  • Genome region :Xp21.3
  • OMIM_ID :300004OMIM phenotype ID
  • OMIM_ID :300382OMIM gene ID
Lissencephaly, X-linked 2, 300215 (3) OMIM high
  • Genome region :Xp21.3
  • OMIM_ID :300215OMIM phenotype ID
  • OMIM_ID :300382OMIM gene ID