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

EIF2B1
(UniProt - OMIM)
 APP
(UniProt - OMIM)
EIF2B2
(UniProt - OMIM)
EIF2B3
(UniProt - OMIM)
EIF2B4
(UniProt - OMIM)
EIF2B5
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
EIF2B2
EIF2B5
(0.56)
(0.56)
APP
APP


Citations in the biomedical literature:


Ovarioleukodystrophy
EIF2B1 EIF2B2 EIF2B3 EIF2B4 EIF2B5
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP



Ovarioleukodystrophy
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Synonym(s):
(no synonyms)

Synonym(s):
- HCHWA, Arctic type
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
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



Ovarioleukodystrophy

(no data available)