ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Cardiomyopathy - hypotonia - lactic acidosis

Autosomal recessive cutis laxa type 2, classic type


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SLC25A3	(0.49)	ATP6V0A2

Citations in the biomedical literature:

Cardiomyopathy - hypotonia - lactic acidosis		Autosomal recessive cutis laxa type 2, classic type
	Synonym(s): (no synonyms)		Synonym(s): - ARCL2, DebrÃ© type - ARCL2, classic type - Autosomal recessive cutis laxa type 2, DebrÃ© type

	Classification (Orphanet): - Inborn errors of metabolism - Rare cardiac disease - Rare genetic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare abdominal surgical disease - Rare bone disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare skin disease - Rare surgical thoracic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	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

No signs/symptoms info available.