Cytoscape Web
Click node...


7 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Posterior polar cataract
X-linked hyper-IgM syndrome

CHMP4B CD40LG
CRYAB
EPHA2
GJA3
PITX3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CRYAB
(0.63)
CD40LG



Citations in the biomedical literature:


Posterior polar cataract
CHMP4B CRYAB EPHA2 GJA3 PITX3
X-linked hyper-IgM syndrome
CD40LG



Posterior polar cataract
X-linked hyper-IgM syndrome

Synonym(s):
- Posterior subcapsular cataract

Synonym(s):
- HIGM1
- Hyper-IgM syndrome due to CD40 ligand deficiency
- Hyper-IgM syndrome due to CD40L deficiency
- Hyper-IgM syndrome type 1
- XHIGM

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

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

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

No signs/symptoms info available.