ODCs

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2 OMIM references -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Acute infantile liver failure-multisystemic involvement syndrome

Amish nemaline myopathy

LARS	(UniProt - OMIM)		TNNT1	(UniProt - OMIM)
MARS	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MARS	(0.63)	TNNT1

Citations in the biomedical literature:

Acute infantile liver failure-multisystemic involvement syndrome		Amish nemaline myopathy

	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: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal recessive

	External references: 2 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.