Diabetes Mellitus, Permanent Neonatal, 2 (PNDM2)

Diabetes Mellitus, Permanent Neonatal, 2(来自ICD-11)

别称:

Diabetes, Permanent Neonatal 2, with or Without Neurologic Features

Diabetes Mellitus, Permanent Neonatal 2

Pndm2

Developmental Delay, Epilepsy, and Neonatal Diabetes 1

Dend1

加入收藏

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Diabetes Mellitus, Permanent Neonatal, 2, is also known as diabetes, permanent neonatal 2, with or without neurologic features. An important gene associated with Diabetes Mellitus, Permanent Neonatal, 2 is KCNJ11 (Potassium Inwardly Rectifying Channel Subfamily J Member 11). Affiliated tissues include pancreas and brain, and related phenotypes are global developmental delay and hypsarrhythmia

查看原文参与反馈