ODCs

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

PROTEIN INTERACTIONS: 1

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

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

Juvenile myelomonocytic leukemia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CSF1R	(0.96)	CBL

Citations in the biomedical literature:

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia		Juvenile myelomonocytic leukemia
	Synonym(s): - ALSP - Autosomal dominant leukoencephalopathy with neuroaxonal spheroids - HDLS - Hereditary diffuse leukoencephalopathy with spheroids - POLD - Pigmentary orthochromatic leukodystrophy		Synonym(s): - Juvenile chronic myelomonocytic leukemia

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Neoplasms -

	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: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D054429

No signs/symptoms info available.