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11 OMIM references -
12 associated genes
No signs/symptoms info
COMMON GENES: 2
PROTEIN INTERACTIONS: 1
3 OMIM references -
5 associated genes
No signs/symptoms info
MODY syndrome
Transient neonatal diabetes mellitus

ABCC8 ABCC8
BLK HYMAI
CEL KCNJ11
GCK PLAGL1
HNF1A ZFP57
HNF4A
INS
KCNJ11
KLF11
NEUROD1
PAX4
PDX1


COMMON
GENES
ABCC8
KCNJ11


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HNF1A
(0.63)
HYMAI



Citations in the biomedical literature:


MODY syndrome
ABCC8 BLK CEL GCK HNF1A HNF4A
INS KCNJ11 KLF11 NEUROD1 PAX4 PDX1

Transient neonatal diabetes mellitus
HYMAI PLAGL1 ZFP57



MODY syndrome
Transient neonatal diabetes mellitus

Synonym(s):
- Maturity-onset diabetes of the young

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: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
11 OMIM references -
No MeSH references
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.