Bilateral striopallidodentate calcinosis

rare

A basal ganglia disease characterized by the accumulation of calcium deposits in different brain regions, particularly the basal ganglia and dentate nucleus, and is often associated with neurodegeneration.

Identifiers: MONDO:0008947 Orphanet:1980
Part of: Basal ganglia disorder Hereditary neurological disease
Also known as: basal ganglia calcification · basal ganglia degeneration with calcification · BSPDC · cerebrovascular ferrocalcinosis · PFBC

Subtypes

All diseases Rare only

Disease	ID	Genes
Basal ganglia calcification, idiopathic, 1	MONDO:0024538	SLC20A2
Basal ganglia calcification, idiopathic, 10, autosomal recessive	MONDO:0975875	CMPK2
Basal ganglia calcification, idiopathic, 11, autosomal recessive	MONDO:0980939	RRP12
Basal ganglia calcification, idiopathic, 4	MONDO:0014004	PDGFRB
Basal ganglia calcification, idiopathic, 5	MONDO:0014204	PDGFB
Basal ganglia calcification, idiopathic, 6	MONDO:0014628	XPR1
Basal ganglia calcification, idiopathic, 7, autosomal recessive	MONDO:0032673	MYORG
Basal ganglia calcification, idiopathic, 8, autosomal recessive	MONDO:0032938	JAM2
Basal ganglia calcification, idiopathic, 9, autosomal recessive	MONDO:0968977	NAA60
Basal ganglia calcification, idiopathic, childhood-onset	MONDO:0007247

Rare disease

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