ODCs

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3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Cerebral sinovenous thrombosis

Atypical hemolytic uremic syndrome with thrombomodulin anomaly


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	F2	(0.9)	THBD

Citations in the biomedical literature:

Cerebral sinovenous thrombosis		Atypical hemolytic uremic syndrome with thrombomodulin anomaly
	Synonym(s): - CSVT		Synonym(s): - Atypical HUS with thrombomodulin anomaly - D-HUS with thrombomodulin anomaly - Hemolytic-uremic syndrome without diarrhea with thrombomodulin anomaly - aHUS with thrombomodulin anomaly

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.