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Familial porencephaly

MONDO:0020496

An instance of porencephaly that is caused by an inherited modification of the individual's genome.

Also known as: hereditary porencephaly, familial porencephalic white matter disease

13 clinical trials for this condition and its sub-types, 0 tagged with Familial porencephaly itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary neurological disease (5772) ↑ Cerebrovascular disorder (3282) ↑ Porencephaly (3)

Sub-types of Familial porencephaly

Brain small vessel disease 1 with or without ocular anomalies 3 trials
Brain small vessel disease 2A, autosomal dominant 1 trial
Brain small vessel disease 2B, autosomal recessive 0 trials
Brain small vessel disease 3 0 trials
Brain small vessel disease 4 0 trials
Brain small vessel disease 5 with osteoporosis 0 trials
Brain small vessel disease 6 with leukoencephalopathy 0 trials

Including sub-types (13) Tagged with Familial porencephaly (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.