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Total congenital cataract
7 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Total congenital cataract
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

CRYBB2
(UniProt - OMIM)
 APP
(UniProt - OMIM)
CRYGB
(UniProt - OMIM)
EPHA2
(UniProt - OMIM)
MIP
(UniProt - OMIM)
NHS
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
EPHA2
(0.56)
APP


Citations in the biomedical literature:


Total congenital cataract
CRYBB2 CRYGB EPHA2 MIP NHS
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Total congenital cataract
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
(no synonyms)

Synonym(s):
- HCHWA, Flemish 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 -
1 MeSH reference: C535341
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.