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DEND syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
DEND syndrome
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency

KCNJ11
(UniProt - OMIM)
 KCNJ11
(UniProt - OMIM)

COMMON
GENES 		KCNJ11


Citations in the biomedical literature:


DEND syndrome
KCNJ11
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency



DEND syndrome
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency

Synonym(s):
- Developmental delay - epilepsy - neonatal diabetes
Synonym(s):
- Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.