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Autosomal dominant hyperinsulinism due to SUR1 deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Transient neonatal diabetes mellitus
3 OMIM references -
5 associated genes
No signs/symptoms info
Autosomal dominant hyperinsulinism due to SUR1 deficiency
Transient neonatal diabetes mellitus

ABCC8
(UniProt - OMIM)
 ABCC8
(UniProt - OMIM)
HYMAI
(OMIM)
KCNJ11
(UniProt - OMIM)
PLAGL1
(UniProt - OMIM)
ZFP57
(UniProt - OMIM)

COMMON
GENES 		ABCC8


Citations in the biomedical literature:


Autosomal dominant hyperinsulinism due to SUR1 deficiency
ABCC8
Transient neonatal diabetes mellitus
HYMAI KCNJ11 PLAGL1 ZFP57



Autosomal dominant hyperinsulinism due to SUR1 deficiency
Transient neonatal diabetes mellitus

Synonym(s):
- Autosomal dominant hyperinsulinemic hypoglycemia due to SUR1 deficiency
Synonym(s):
- TNDM
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Certain conditions originating in the perinatal period -
Epidemiological data:
Class of prevalence: unknown
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:
3 OMIM references -
No MeSH references
No signs/symptoms info available.