Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 658
  • Symbol: BMPR1B
  • Description: bone morphogenetic protein receptor type 1B

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Disease_Term Source Rank Other Values
Brachydactyly, type A2, 112600 (3) OMIM high
  • Genome region : 20p12.3
  • Genome region : 20q11.22
  • Genome region : 4q22.3
  • OMIM_ID : 112261 OMIM gene ID
  • OMIM_ID : 112600 OMIM phenotype ID
  • OMIM_ID : 601146 OMIM gene ID
  • OMIM_ID : 603248 OMIM gene ID
Brachydactyly, type A1, D, 616849 (3) OMIM high
  • Genome region : 4q22.3
  • OMIM_ID : 603248 OMIM gene ID
  • OMIM_ID : 616849 OMIM phenotype ID
Acromesomelic dysplasia, Demirhan type, 609441 (3) OMIM high
  • Genome region : 4q22.3
  • OMIM_ID : 603248 OMIM gene ID
  • OMIM_ID : 609441 OMIM phenotype ID
Amyotrophic lateral sclerosis (sporadic) GWAS high
Attention deficit hyperactivity disorder GWAS high