Log In|Sign Up
ENDiabetes Mellitus, Permanent Neonatal, 3 (PNDM3)
Alias:
Diabetes Mellitus, Permanent Neonatal 3, with or Without Neurologic Features
Diabetes Mellitus, Permanent Neonatal 3
Pndm3
Diabetes, Permanent Neonatal 3, with or Without Neurologic Features
Developmental Delay, Epilepsy, and Neonatal Diabetes 2
Dend2
Favorite
Diabetes Mellitus, Permanent Neonatal, 3, is also known as diabetes mellitus, permanent neonatal 3, with or without neurologic features. An important gene associated with Diabetes Mellitus, Permanent Neonatal, 3 is ABCC8 (ATP Binding Cassette Subfamily C Member 8). Related phenotypes are muscle weakness and type i diabetes mellitus
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
