EFNB1, ephrin B1, 1947

N. diseases: 134; N. variants: 19
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 8 18 1.000 None 0.958 24 18 2004 2019