Brain small vessel disease 1 with or without ocular anomalies

MONDO:0008289

Any porencephaly in which the cause of the disease is a mutation in the COL4A1 gene.

Also known as: ADT1P, BSVD, BSVD1, COL4A1 porencephaly, COL4A1-related brain small vessel disease with haemorrhage, T1P, brain small vessel disease with axenfeld-rieger anomaly, brain small vessel disease with haemorrhage

13 clinical trials for this condition and its sub-types, 3 tagged with Brain small vessel disease 1 with or without ocular anomalies itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

Including sub-types (13) Tagged with Brain small vessel disease 1 with or without ocular anomalies (3)

Trials to join now! 2 Not yet recruiting 1

French biobank aims to unlock secrets of rare brain vessel diseases

Knowledge-focused Not yet recruiting

This study will collect blood samples and medical information from 600 adults with rare diseases affecting blood vessels in the brain and eye, such as CADASIL and cavernous angioma. The goal is to create a long-term biobank that researchers can use to find biomarkers and better u…

Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Knowledge-focused

Last updated Jun 27, 2026 14:00 UTC

Brain small vessel disease 1 with or without ocular anomalies

Where it sits in the disease tree

French biobank aims to unlock secrets of rare brain vessel diseases