DISEASES

Disease-gene associations mined from literature

Human genes for DOID:4019

DOID:4019 [DOID:4019]

Apraxia is a disorder caused by damage to specific areas of the cerebrum. Apraxia is characterized by loss of the ability to execute or carry out learned purposeful movements, despite having the desire and the physical ability to perform the movements. It is a disorder of motor planning, which may be acquired or developmental, but may not be caused by incoordination, sensory loss, or failure to comprehend simple commands (which can be tested by asking the person to recognize the correct movement from a series). Apraxia should not be confused with ataxia, a lack of coordination of movements, aphasia, an inability to produce and/or comprehend language; abulia, the lack of desire to carry out an action; or allochiria, in which patients perceive stimuli to one side of the body as occurring on the other.

Synonyms:  apraxia,  DOID:4019,  Apraxia (context-dependent category),  Apraxia (finding),  Apraxia [Ambiguous] ...