Diabetes Mellitus, Permanent Neonatal, 1 (PNDM1)

Alias:

Permanent Diabetes Mellitus of Infancy

Permanent Neonatal Diabetes Mellitus 1

Dend Syndrome

Pndm1

Pdmi

Diabetes Mellitus Permanent Neonatal with Neurologic Features

Developmental Delay-Epilepsy-Neonatal Diabetes Syndrome

Developmental Delay, Epilepsy, and Neonatal Diabetes

Developmental Delay Epilepsy and Neonatal Diabetes

Diabetes Mellitus, Permanent Neonatal, Type 1

Diabetes Mellitus, Permanent, of Infancy

Diabetes Mellitus, Permanent Neonatal 1

Dend

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Diabetes Mellitus, Permanent Neonatal, 1, also known as permanent diabetes mellitus of infancy, is related to diabetes mellitus, permanent neonatal, 4 and isolated permanent neonatal diabetes mellitus. An important gene associated with Diabetes Mellitus, Permanent Neonatal, 1 is GCK (Glucokinase), and among its related pathways/superpathways are Integration of energy metabolism and Disorders of transmembrane transporters. The drug Glyburide has been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle and pancreas, and related phenotypes are hyperglycemia and elevated hemoglobin a1c

Related ID：

MALACARDS：DBT104

OMIM：606176

MESH：D003920