Intermediate Dend Syndrome

Alias:
Developmental Delay-Epilepsy-Neonatal Diabetes Syndrome, Intermediate Form
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Intermediate Dend Syndrome, also known as developmental delay-epilepsy-neonatal diabetes syndrome, intermediate form, is related to permanent neonatal diabetes mellitus and diabetes mellitus, permanent neonatal, 1. An important gene associated with Intermediate Dend Syndrome is KCNJ11 (Potassium Inwardly Rectifying Channel Subfamily J Member 11).
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
AD
Newborn
--
1
17
--

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
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