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8 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Fuchs endothelial corneal dystrophy
Parathyroid carcinoma

AGBL1 CDC73
COL8A2
SLC4A11
TCF4
ZEB1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TCF4
(0.7)
CDC73



Citations in the biomedical literature:


Fuchs endothelial corneal dystrophy
AGBL1 COL8A2 SLC4A11 TCF4 ZEB1
Parathyroid carcinoma
CDC73



Fuchs endothelial corneal dystrophy
Parathyroid carcinoma

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

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Diseases of the eye and adnexa -
Classification (ICD10):
- Neoplasms -

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:
8 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.