Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:5979
  • Symbol:RET
  • Description:ret proto-oncogene

Export (tab separated) Export to Excel

Disease_Term Source Rank Other Values
Central hypoventilation syndrome, congenital, 209880 (3) OMIM high
  • Genome region :10q11.21
  • Genome region :11p14.1
  • Genome region :12q23.2
  • Genome region :20q13.32
  • OMIM_ID :100790OMIM gene ID
  • OMIM_ID :113505OMIM gene ID
  • OMIM_ID :131242OMIM gene ID
  • OMIM_ID :164761OMIM gene ID
  • OMIM_ID :209880OMIM phenotype ID
Multiple endocrine neoplasia IIB, 162300 (3) OMIM high
  • Genome region :10q11.21
  • OMIM_ID :162300OMIM phenotype ID
  • OMIM_ID :164761OMIM gene ID
Pheochromocytoma, 171300 (3) OMIM high
  • Genome region :10q11.21
  • Genome region :11q23.1
  • Genome region :1p36.13
  • Genome region :1p36.22
  • Genome region :3p25.3
  • OMIM_ID :164761OMIM gene ID
  • OMIM_ID :171300OMIM phenotype ID
  • OMIM_ID :185470OMIM gene ID
  • OMIM_ID :602690OMIM gene ID
  • OMIM_ID :605995OMIM gene ID
  • OMIM_ID :608537OMIM gene ID
{Hirschsprung disease, susceptibility to, 1}, 142623 (3) OMIM high
  • Genome region :10q11.21
  • OMIM_ID :142623OMIM phenotype ID
  • OMIM_ID :164761OMIM gene ID
Medullary thyroid carcinoma, 155240 (3) OMIM high
  • Genome region :10q11.21
  • OMIM_ID :155240OMIM phenotype ID
  • OMIM_ID :164761OMIM gene ID
Multiple endocrine neoplasia IIA, 171400 (3) OMIM high
  • Genome region :10q11.21
  • OMIM_ID :164761OMIM gene ID
  • OMIM_ID :171400OMIM phenotype ID
Hirschsprung disease GWAS high
Cannabis dependence GWAS high