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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
/
Hereditary neurological disease
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Bilateral striopallidodentate calcinosis
Basal ganglia calcification, idiopathic, 10, autosomal recessive
rare
Identifiers
MONDO:0975875
OMIM:621018
Causal genes
CMPK2
Part of
Bilateral striopallidodentate calcinosis
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