ABCC8 - ATP-binding cassette, sub-family C (CFTR/MRP), member 8
|
|
Diseases list
- Disease-causing germline mutation(s) in Autosomal dominant hyperinsulinism due to SUR1 deficiency
- Disease-causing germline mutation(s) in Autosomal recessive hyperinsulinism due to SUR1 deficiency
- Disease-causing germline mutation(s) in Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency
- Disease-causing germline mutation(s) in MODY syndrome
- Disease-causing germline mutation(s) in Permanent neonatal diabetes mellitus
- Disease-causing germline mutation(s) in Transient neonatal diabetes mellitus
Assessed
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
