Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:2261
  • Symbol:FGFR3
  • Description:fibroblast growth factor receptor 3

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Disease_Term Source Rank Other Values
Bladder cancer, somatic, 109800 (3) OMIM high
  • Genome region :12p12.1
  • Genome region :13q14.2
  • Genome region :4p16.3
  • OMIM_ID :109800OMIM phenotype ID
  • OMIM_ID :134934OMIM gene ID
  • OMIM_ID :190070OMIM gene ID
  • OMIM_ID :614041OMIM gene ID
Spermatocytic seminoma, somatic, 273300 (3) OMIM high
  • Genome region :4p16.3
  • OMIM_ID :134934OMIM gene ID
  • OMIM_ID :273300OMIM phenotype ID
Crouzon syndrome with acanthosis nigricans, 612247 (3) OMIM high
  • Genome region :4p16.3
  • OMIM_ID :134934OMIM gene ID
  • OMIM_ID :612247OMIM phenotype ID
Muenke syndrome, 602849 (3) OMIM high
  • Genome region :4p16.3
  • OMIM_ID :134934OMIM gene ID
  • OMIM_ID :602849OMIM phenotype ID
CATSHL syndrome, 610474 (3) OMIM high
  • Genome region :4p16.3
  • OMIM_ID :134934OMIM gene ID
  • OMIM_ID :610474OMIM phenotype ID
Thanatophoric dysplasia, type I, 187600 (3) OMIM high
  • Genome region :4p16.3
  • OMIM_ID :134934OMIM gene ID
  • OMIM_ID :187600OMIM phenotype ID
Achondroplasia, 100800 (3) OMIM high
  • Genome region :4p16.3
  • OMIM_ID :100800OMIM phenotype ID
  • OMIM_ID :134934OMIM gene ID
Nevus, epidermal, somatic, 162900 (3) OMIM high
  • Genome region :3q26.32
  • Genome region :4p16.3
  • OMIM_ID :134934OMIM gene ID
  • OMIM_ID :162900OMIM phenotype ID
  • OMIM_ID :171834OMIM gene ID
Cervical cancer, somatic, 603956 (3) OMIM high
  • Genome region :4p16.3
  • OMIM_ID :134934OMIM gene ID
  • OMIM_ID :603956OMIM phenotype ID
Thanatophoric dysplasia, type II, 187601 (3) OMIM high
  • Genome region :4p16.3
  • OMIM_ID :134934OMIM gene ID
  • OMIM_ID :187601OMIM phenotype ID
Hypochondroplasia, 146000 (3) OMIM high
  • Genome region :4p16.3
  • OMIM_ID :134934OMIM gene ID
  • OMIM_ID :146000OMIM phenotype ID
SADDAN, 616482 (3) OMIM high
  • Genome region :4p16.3
  • OMIM_ID :134934OMIM gene ID
  • OMIM_ID :616482OMIM phenotype ID
Colorectal cancer, somatic, 114500 (3) OMIM high
  • Genome region :14q24.3
  • Genome region :14q32.33
  • Genome region :15q15.1
  • Genome region :17p11.2
  • Genome region :17q24.1
  • Genome region :18q21.2
  • Genome region :19q13.33
  • Genome region :1p13.2
  • Genome region :22q13.2
  • Genome region :3p22.1
  • Genome region :3q26.32
  • Genome region :4p16.3
  • Genome region :5q22.2
  • Genome region :8p22
  • OMIM_ID :114500OMIM phenotype ID
  • OMIM_ID :116806OMIM gene ID
  • OMIM_ID :120470OMIM gene ID
  • OMIM_ID :134934OMIM gene ID
  • OMIM_ID :159350OMIM gene ID
  • OMIM_ID :164730OMIM gene ID
  • OMIM_ID :164790OMIM gene ID
  • OMIM_ID :171834OMIM gene ID
  • OMIM_ID :600040OMIM gene ID
  • OMIM_ID :602700OMIM gene ID
  • OMIM_ID :602860OMIM gene ID
  • OMIM_ID :604025OMIM gene ID
  • OMIM_ID :604258OMIM gene ID
  • OMIM_ID :604395OMIM gene ID
  • OMIM_ID :604584OMIM gene ID
  • OMIM_ID :607273OMIM gene ID
  • OMIM_ID :611731OMIM gene ID
LADD syndrome, 149730 (3) OMIM high
  • Genome region :10q26.13
  • Genome region :4p16.3
  • Genome region :5p12
  • OMIM_ID :134934OMIM gene ID
  • OMIM_ID :149730OMIM phenotype ID
  • OMIM_ID :176943OMIM gene ID
  • OMIM_ID :602115OMIM gene ID
Height GWAS high
Bladder cancer GWAS high
Urinary bladder cancer GWAS high