Cytoscape Web
Click node...

Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
1 OMIM reference -
1 associated gene
3 signs/symptoms
Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

MCEE
(UniProt - OMIM)
 APP
(UniProt - OMIM)

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


Citations in the biomedical literature:


Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency
MCEE
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP



Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Synonym(s):
- MCEE deficiency
- Methylmalonic acidemia due to methylmalonyl-CoA racemase deficiency
- Methylmalonic aciduria due to methylmalonyl-CoA epimerase deficiency
- Methylmalonic aciduria due to methylmalonyl-CoA racemase deficiency
Synonym(s):
- HCHWA, Arctic type
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic 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



Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency

(no data available)