Associated diseases in AS-tDR-011775


DiseaseDO_IDDO_NameDO_TypeDO_Define
Alzheimer DiseaseDOID:10652Alzheimer's diseasedisease of anatomical entityA tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.
Amyotrophic Lateral SclerosisDOID:332amyotrophic lateral sclerosisdisease of anatomical entityA motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing.
Brain Injuries, TraumaticDOID:0081292traumatic brain injurydisease of anatomical entityA brain disease that is characterized by brain dysfunction caused by an outside force, usually a violent blow to the head.
Carotid Artery InjuriesDOID:3407carotid artery diseasedisease of anatomical entityN/A
Depressive Disorder, MajorDOID:1470major depressive disorderdisease of mental healthA depressive disorder that is characterized by at least two weeks of loss of interest or pleasure in normally enjoyable activities or depressed mood along with additional cognitive or somatic impairments such as appetite or weight changes, sleep difficulties, psychomotor agitation or retardation, fatigue or loss of energy, diminished ability to think or concentrate, feelings of worthlessness or excessive guilt, and suicidality.
Diffuse Intrinsic Pontine GliomaDOID:0080880diffuse glioma, H3 G34 mutantdisease of cellular proliferationA histone mutated tumor that has_material_basis_in mutations in codon 34 of the H3 histone family 3A protein.
EpilepsyDOID:1826epilepsydisease of anatomical entityA brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.
Intracranial AneurysmDOID:10941intracranial aneurysmdisease of anatomical entity//nervous system diseaseN/A
Moyamoya diseaseDOID:13099Moyamoya diseasedisease of anatomical entity//nervous system diseaseA cerebral arterial disease characterized by constriction of certain arteries at the base of the brain. Blood flow is blocked by the constriction and also by blood clots.
Moyamoya DiseaseDOID:13099Moyamoya diseasedisease of anatomical entity//nervous system diseaseA cerebral arterial disease characterized by constriction of certain arteries at the base of the brain. Blood flow is blocked by the constriction and also by blood clots.
Multiple SclerosisDOID:2377multiple sclerosisdisease of anatomical entity//nervous system diseaseA demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring.
Neurodegenerative DiseasesDOID:1289neurodegenerative diseasedisease of anatomical entityA central nervous system disease that results in the progressive deterioration of function or structure of neurons.
Parkinson DiseaseDOID:14330Parkinson's diseasedisease of anatomical entityA synucleinopathy that has_material_basis_in degeneration of the central nervous system that often impairs motor skills, speech, and other functions.
Sleep Apnea, ObstructiveDOID:0050848obstructive sleep apneadisease of mental healthA sleep apnea that is characterized by repeated collapse and obstruction of the upper airway during sleep, which results in reduced airflow (hypopnea) or complete airflow cessation (apnea), oxygen desaturation, and arousals from sleep.
Spinal Cord InjuriesN/AN/AN/AN/A
StrokeN/AN/AN/AN/A