Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:4854
  • Symbol:NOTCH3
  • Description:notch receptor 3

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Disease_Term Source Rank Other Values
Lateral meningocele syndrome, 130720 (3) OMIM high
  • Genome region :19p13.12
  • OMIM_ID :130720OMIM phenotype ID
  • OMIM_ID :600276OMIM gene ID
Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1, 125310 (3) OMIM high
  • Genome region :19p13.12
  • OMIM_ID :125310OMIM phenotype ID
  • OMIM_ID :600276OMIM gene ID
?Myofibromatosis, infantile 2, 615293 (3) OMIM high
  • Genome region :19p13.12
  • OMIM_ID :600276OMIM gene ID
  • OMIM_ID :615293OMIM phenotype ID