CENPF, centromere protein F, 1063

N. diseases: 76; N. variants: 10
Disease: Jejunal Atresia with Microcephaly and Ocular Anomalies ×
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: C1855705
Disease: Jejunal Atresia with Microcephaly and Ocular Anomalies
Jejunal Atresia with Microcephaly and Ocular Anomalies 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 1 9 0.720 None 1.000 4 9 2015 2020