DISEASES

Disease-gene associations mined from literature

Human genes for pseudobulbar palsy

Pseudobulbar palsy [DOID:12680]

An autosomal dominant disease characterized by the presence of multiple arteriovenous malformations that lack intervening capillaries and result in direct connections between arteries and veins.

Synonyms:  pseudobulbar palsy,  DOID:12680,  Pseudobulbar palsy (disorder),  pseudobulbar paralysis,  Pseudobulbar palsy