ABCC8
ATP binding cassette subfamily C member 8
Ассоциированные заболевания
Герминативная мутация (причина)7
Autosomal dominant hyperinsulinism due to SUR1 deficiencyORPHA:276575
→Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiencyORPHA:276598
→MODYORPHA:552
→DEND syndromeORPHA:79134
→Autosomal recessive hyperinsulinism due to SUR1 deficiencyORPHA:79643
→Isolated permanent neonatal diabetes mellitusORPHA:99885
→Transient neonatal diabetes mellitusORPHA:99886
→