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11 OMIM references -
12 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
5 signs/symptoms
MODY syndrome
Partial pancreatic agenesis

ABCC8 PDX1
BLK PTF1A
CEL
GCK
HNF1A
HNF4A
INS
KCNJ11
KLF11
NEUROD1
PAX4
PDX1


COMMON
GENES
PDX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NEUROD1
(0.52)
PDX1



Citations in the biomedical literature:


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

Partial pancreatic agenesis
PTF1A



MODY syndrome
Partial pancreatic agenesis

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

Synonym(s):
- Congenital pancreatic agenesis
- Partial agenesis of the pancreas

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

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

Partial pancreatic agenesis

Very frequent
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Insulin-dependent / type 1 diabetes
- Intrauterine growth retardation
- Maternal diabetes
- Structural anomalies of the pancreas



MODY syndrome

(no data available)