Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:2260
  • Symbol:FGFR1
  • Description:fibroblast growth factor receptor 1

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Disease_Term Source Rank Other Values
Hartsfield syndrome, 615465 (3) OMIM high
  • Genome region :8p11.23
  • OMIM_ID :136350OMIM gene ID
  • OMIM_ID :615465OMIM phenotype ID
Pfeiffer syndrome, 101600 (3) OMIM high
  • Genome region :10q26.13
  • Genome region :8p11.23
  • OMIM_ID :101600OMIM phenotype ID
  • OMIM_ID :136350OMIM gene ID
  • OMIM_ID :176943OMIM gene ID
Hypogonadotropic hypogonadism 2 with or without anosmia, 147950 (3) OMIM high
  • Genome region :8p11.23
  • OMIM_ID :136350OMIM gene ID
  • OMIM_ID :147950OMIM phenotype ID
Jackson-Weiss syndrome, 123150 (3) OMIM high
  • Genome region :10q26.13
  • Genome region :8p11.23
  • OMIM_ID :123150OMIM phenotype ID
  • OMIM_ID :136350OMIM gene ID
  • OMIM_ID :176943OMIM gene ID
Trigonocephaly 1, 190440 (3) OMIM high
  • Genome region :8p11.23
  • OMIM_ID :136350OMIM gene ID
  • OMIM_ID :190440OMIM phenotype ID
Encephalocraniocutaneous lipomatosis, 613001 (3) OMIM high
  • Genome region :8p11.23
  • OMIM_ID :136350OMIM gene ID
  • OMIM_ID :613001OMIM phenotype ID
Osteoglophonic dysplasia, 166250 (3) OMIM high
  • Genome region :8p11.23
  • OMIM_ID :136350OMIM gene ID
  • OMIM_ID :166250OMIM phenotype ID
Response to cognitive-behavioural therapy in anxiety disorder GWAS high