Cytoscape Web
Click node...


7 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 OMIM reference -
1 associated gene
3 signs/symptoms
Posterior polar cataract
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

CHMP4B APP
CRYAB
EPHA2
GJA3
PITX3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CRYAB
EPHA2
(0.81)
(0.56)
APP
APP



Citations in the biomedical literature:


Posterior polar cataract
CHMP4B CRYAB EPHA2 GJA3 PITX3
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP



Posterior polar cataract
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Synonym(s):
- Posterior subcapsular cataract

Synonym(s):
- HCHWA, Arctic type

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

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

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

Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Very frequent
- Autosomal dominant inheritance
- Psychic / behavioural troubles
- Psychic / psychomotor regression / dementia / intellectual decline



Posterior polar cataract

(no data available)