ABCD syndrome

MONDO:0010895

An autosomal recessive disease that is characterized by albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness and has material basis in a mutation in the endothelin B receptor gene (EDNRB).

Also known as: ABCD syndrome, albinism, block lock, cell migration disorder of the neurocytes of the gut, and deafness, ABCDS, albinism, black lock, cell migration disorder of the Neurocytes of the gut, and deafness

0 clinical trials for this condition and its sub-types, 0 tagged with ABCD syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal recessive disease (994)

Including sub-types (0) Tagged with ABCD syndrome (0)

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