Human genes for ABCD syndrome
ABCD syndrome [DOID:0050600]
A syndrome 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).
Synonyms: ABCD syndrome, ABCD disease, ABCD disorder, ABCD syndromes, DOID:0050600 ...
Linkouts: OMIM