Cytoscape Web
Click node...


13 OMIM references -
14 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
7 OMIM references -
5 associated genes
No signs/symptoms info
Autosomal dominant nonsyndromic intellectual deficit
Posterior polar cataract

CACNG2 CHMP4B
CDH15 CRYAB
CTNNB1 EPHA2
DOCK8 GJA3
DYNC1H1 PITX3
DYRK1A
EPB41L1
GRIN1
GRIN2B
KIF1A
KIRREL3
MBD5
SYNGAP1
TCF4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
(0.84)
CRYAB



Citations in the biomedical literature:


Autosomal dominant nonsyndromic intellectual deficit
CACNG2 CDH15 CTNNB1 DOCK8 DYNC1H1 DYRK1A
EPB41L1 GRIN1 GRIN2B KIF1A KIRREL3 MBD5
SYNGAP1 TCF4
Posterior polar cataract
CHMP4B CRYAB EPHA2 GJA3 PITX3



Autosomal dominant nonsyndromic intellectual deficit
Posterior polar cataract

Synonym(s):
(no synonyms)

Synonym(s):
- Posterior subcapsular cataract

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
13 OMIM references -
No MeSH references
External references:
7 OMIM references -
No MeSH references

No signs/symptoms info available.