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13 OMIM references -
14 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
8 OMIM references -
5 associated genes
No signs/symptoms info
Autosomal dominant nonsyndromic intellectual deficit
Fuchs endothelial corneal dystrophy

CACNG2 AGBL1
CDH15 COL8A2
CTNNB1 SLC4A11
DOCK8 TCF4
DYNC1H1 ZEB1
DYRK1A
EPB41L1
GRIN1
GRIN2B
KIF1A
KIRREL3
MBD5
SYNGAP1
TCF4


COMMON
GENES
TCF4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
(0.9)
TCF4



Citations in the biomedical literature:


Autosomal dominant nonsyndromic intellectual deficit
CACNG2 CDH15 CTNNB1 DOCK8 DYNC1H1 DYRK1A
EPB41L1 GRIN1 GRIN2B KIF1A KIRREL3 MBD5
SYNGAP1 TCF4
Fuchs endothelial corneal dystrophy
AGBL1 COL8A2 SLC4A11 ZEB1



Autosomal dominant nonsyndromic intellectual deficit
Fuchs endothelial corneal dystrophy

Synonym(s):
(no synonyms)

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

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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the eye and adnexa -

Epidemiological data:
Class of prevalence: -
Average age onset: -
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:
13 OMIM references -
No MeSH references
External references:
8 OMIM references -
No MeSH references

No signs/symptoms info available.