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   Chromosome: X (208 OMIM diseases)   Display all OMIM diseases on Chr:
  
  Ensembl id   HUGO id   OMIM id   Chromosome   Cytolocation
Aarskog-Scott syndrome (3)
  ENSG00000102302     FGD1     305400     X     p11.21
  No ensembl prediction     FGDY     305400     X     p11.21
  No ensembl prediction     AAS     305400     X     p11.21
Adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism (3)
  No ensembl prediction     AHC     300200     X     p21.3 - p21.2
  No ensembl prediction     DAX1     300200     X     p21.3 - p21.2
  No ensembl prediction     AHX     300200     X     p21.3 - p21.2
Adrenoleukodystrophy (3)
  No ensembl prediction     ALD     300100     X     q28
Adrenomyeloneuropathy (3)
  No ensembl prediction     ALD     300100     X     q28
Agammaglobulinemia, type 1, X-linked (3)
  ENSG00000010671     BTK     300300     X     q21.3 - q22
  No ensembl prediction     AGMX1     300300     X     q21.3 - q22
  No ensembl prediction     IMD1     300300     X     q21.3 - q22
  No ensembl prediction     XLA     300300     X     q21.3 - q22
  No ensembl prediction     AT     300300     X     q21.3 - q22
Agammaglobulinemia, type 2, X-linked (2)
  No ensembl prediction     AGMX2     300310     X     p22
  No ensembl prediction     XLA2     300310     X     p22
  No ensembl prediction     IMD6     300310     X     p22
Aicardi syndrome (2)
  No ensembl prediction     AIC     304050     X     p22
Albinism-deafness syndrome (2)
  No ensembl prediction     ADFN     300700     X     q26.3 - q27.1
  No ensembl prediction     ALDS     300700     X     q26.3 - q27.1

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 Date : 2001-10-30 16:35:30 Help Desk / Suggestions