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

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

Capillary malformation - arteriovenous malformation


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CSF1R	(0.52)	RASA1

Citations in the biomedical literature:

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia		Capillary malformation - arteriovenous malformation
	Synonym(s): - ALSP - Autosomal dominant leukoencephalopathy with neuroaxonal spheroids - HDLS - Hereditary diffuse leukoencephalopathy with spheroids - POLD - Pigmentary orthochromatic leukodystrophy		Synonym(s): - CM-AVM

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare circulatory system disease - Rare developmental defect during embryogenesis - Rare genetic disease

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: adult Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.