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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Familial porencephaly
Brain small vessel disease 2B, autosomal recessive
rare
Identifiers
MONDO:0980747
OMIM:621414
Causal genes
COL4A2
Part of
Autosomal recessive disease
Familial porencephaly
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