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

CADDS

Hereditary cerebral hemorrhage with amyloidosis, Flemish type

ABCD1	(UniProt - OMIM)		APP	(UniProt - OMIM)
BCAP31	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	BCAP31	(0.77)	APP

Citations in the biomedical literature:

CADDS		Hereditary cerebral hemorrhage with amyloidosis, Flemish type
	Synonym(s): - Contiguous ABCD1 DXS1357E deletion syndrome - Zellweger-like contiguous gene deletion syndrome		Synonym(s): - HCHWA, Flemish type

	Classification (Orphanet): - Inborn errors of metabolism - Rare developmental defect during embryogenesis - Rare genetic disease - Rare hepatic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: sporadic		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.