Cytoscape Web
Click node...

Multiple acyl-CoA dehydrogenation deficiency, mild type
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
1 OMIM reference -
1 associated gene
3 signs/symptoms
Multiple acyl-CoA dehydrogenation deficiency, mild type
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

ETFA
(UniProt - OMIM)
 APP
(UniProt - OMIM)
ETFB
(UniProt - OMIM)
ETFDH
(UniProt - OMIM)

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


Citations in the biomedical literature:


Multiple acyl-CoA dehydrogenation deficiency, mild type
ETFA ETFB ETFDH
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP



Multiple acyl-CoA dehydrogenation deficiency, mild type
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Synonym(s):
(no synonyms)

Synonym(s):
- HCHWA, Arctic type
Classification (Orphanet):
- Inborn errors of metabolism
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No 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



Multiple acyl-CoA dehydrogenation deficiency, mild type

(no data available)