DISEASES

Disease-gene associations mined from literature

Human genes for pseudobulbar palsy

Pseudobulbar palsy [DOID:12680]

A brain disease that is characterized by damage to neurons of the corticobulbar tract, has_symptom dysarthria, has_symptom dysphagia, has_symptom spasticity located_in tongue, has_symptom abnormal bulbar reflexes, and has_symptom emotional outbursts.

Synonyms:  pseudobulbar palsy,  DOID:12680,  pseudobulbar palsies,  pseudobulbar paralysis,  pseudobulbar paralysises