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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 1
3 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Situs inversus totalis

APP CCDC11
CITED2
NODAL


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
CCDC11



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP
Situs inversus totalis
CCDC11 CITED2 NODAL



Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Situs inversus totalis

Synonym(s):
- HCHWA, Arctic type

Synonym(s):
- Complete situs inversus
- Complete situs inversus viscerum
- Situs inversus

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

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

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

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

Hereditary cerebral hemorrhage with amyloidosis, Arctic type

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



Situs inversus totalis

(no data available)