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Acute infantile liver failure-multisystemic involvement syndrome
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant Charcot-Marie-Tooth disease type 2N
1 OMIM reference -
1 associated gene
No signs/symptoms info
Acute infantile liver failure-multisystemic involvement syndrome
Autosomal dominant Charcot-Marie-Tooth disease type 2N

LARS
(UniProt - OMIM)
 AARS
(UniProt - OMIM)
MARS
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
LARS
(0.56)
AARS


Citations in the biomedical literature:


Acute infantile liver failure-multisystemic involvement syndrome
LARS MARS
Autosomal dominant Charcot-Marie-Tooth disease type 2N
AARS



Acute infantile liver failure-multisystemic involvement syndrome
Autosomal dominant Charcot-Marie-Tooth disease type 2N

Synonym(s):
(no synonyms)

Synonym(s):
- CMT2N
Classification (Orphanet):
- Rare genetic disease
- Rare hepatic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.