ODCs

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4 OMIM references -
3 associated genes
12 signs/symptoms

COMMON GENES: 1
PROTEIN INTERACTIONS: 3

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

Bilateral striopallidodentate calcinosis

Idiopathic hypereosinophilic syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PDGFB PDGFRB PDGFB	(0.9) (0.9) (0.88)	PDGFRA PDGFRA PDGFRB

Citations in the biomedical literature:

Bilateral striopallidodentate calcinosis		Idiopathic hypereosinophilic syndrome
	Synonym(s): - BSPDC - Cerebrovascular ferrocalcinosis - Idiopathic basal ganglia calcification		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

Bilateral striopallidodentate calcinosis
	Very frequent - Agyria / micro / pachy / macrogyria / lissencephaly / gyration / neuronal migration defect - Autosomal recessive inheritance - Dilated cerebral ventricles without hydrocephaly - Hepatomegaly / liver enlargement (excluding storage disease) - Intracranial / cerebral calcifications - Intrauterine growth retardation - Microcephaly - Purpura / petichiae - Seizures / epilepsy / absences / spasms / status epilepticus - Thrombocytopenia / thrombopenia Frequent - Corneal clouding / opacity / vascularisation - Structural anomalies of the liver and the biliary tract
Idiopathic hypereosinophilic syndrome
(no data available)