ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Mitochondrial trifunctional protein deficiency

Hereditary cerebral hemorrhage with amyloidosis, Flemish type

HADHA	(UniProt - OMIM)		APP	(UniProt - OMIM)
HADHB	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HADHB	(0.62)	APP

Citations in the biomedical literature:

Mitochondrial trifunctional protein deficiency		Hereditary cerebral hemorrhage with amyloidosis, Flemish type
	Synonym(s): - TFP deficiency - TFPD		Synonym(s): - HCHWA, Flemish 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): - Diseases of the nervous system -		Classification (ICD10): (no data available)

	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		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: D024741		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.