ODCs

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3 OMIM references -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Idiopathic aplastic anemia

Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SBDS	(0.63)	IDH1

Citations in the biomedical literature:

Idiopathic aplastic anemia		Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria
	Synonym(s): - Bone marrow failure		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare hematologic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adulthood Average age of death: adult Type of inheritance: unknown		Epidemiological data: (no data available)

	External references: 3 OMIM references - 1 MeSH reference: C538494		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.