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Autosomal recessive hyperinsulinism due to Kir6.2 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 recessive hyperinsulinism due to Kir6.2 deficiency
Transient neonatal diabetes mellitus

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

COMMON
GENES 		KCNJ11


Citations in the biomedical literature:


Autosomal recessive hyperinsulinism due to Kir6.2 deficiency
KCNJ11
Transient neonatal diabetes mellitus
ABCC8 HYMAI PLAGL1 ZFP57



Autosomal recessive hyperinsulinism due to Kir6.2 deficiency
Transient neonatal diabetes mellitus

Synonym(s):
- Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 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:
(no data available)
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.