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11 OMIM references -
12 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
8 OMIM references -
5 associated genes
No signs/symptoms info
MODY syndrome
Fuchs endothelial corneal dystrophy

ABCC8 AGBL1
BLK COL8A2
CEL SLC4A11
GCK TCF4
HNF1A ZEB1
HNF4A
INS
KCNJ11
KLF11
NEUROD1
PAX4
PDX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NEUROD1
(0.52)
TCF4



Citations in the biomedical literature:


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

Fuchs endothelial corneal dystrophy
AGBL1 COL8A2 SLC4A11 TCF4 ZEB1



MODY syndrome
Fuchs endothelial corneal dystrophy

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

Synonym(s):
- Endoepithelial corneal dystrophy
- FECD
- Late hereditary endothelial dystrophy

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the eye and adnexa -

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: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.