SPTA1, spectrin alpha, erythrocytic 1, 6708

N. diseases: 76; N. variants: 71
Disease: ELLIPTOCYTOSIS 2 (disorder) ×
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: C1851741
Disease: ELLIPTOCYTOSIS 2 (disorder)
ELLIPTOCYTOSIS 2 (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 1 16 0.700 strong 1.000 13 16 1989 1996