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11 OMIM references -
12 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 3
2 associated genes
No signs/symptoms info
MODY syndrome
Hepatocellular carcinoma, childhood-onset

ABCC8 CTNNB1
BLK MET
CEL
GCK
HNF1A
HNF4A
INS
KCNJ11
KLF11
NEUROD1
PAX4
PDX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HNF4A
BLK
HNF1A
(0.78)
(0.72)
(0.63)
CTNNB1
MET
CTNNB1



Citations in the biomedical literature:


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

Hepatocellular carcinoma, childhood-onset
CTNNB1 MET



MODY syndrome
Hepatocellular carcinoma, childhood-onset

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

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare hepatic disease
- Rare oncologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic

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

No signs/symptoms info available.