医
China Med Service
Best doctors, yours
Breaking down language, channel and process barriers in cross-border care — making the best doctors your personal doctors.
300 Grade-A partner hospitals · 3,000+ leading experts · one-stop service across all specialties
Periodic ataxia (episodic ataxia) (G11.100x004) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compil
Spinocerebellar ataxia (SCA) is autosomal dominant progressive ataxia from cerebellar/brainstem/spinal degeneration; many genetic subtypes; supportive/rehab.
神经内科Early-onset cerebellar ataxia (G11.100) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Congenital imbalance syndrome (G11.000x008) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Congenital ataxia with mental retardation and partial aniridia (G11.000x007) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological
Congenital cerebellar-granule-cell aplasia (G11.000x006) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is bei
Congenital cerebellar-vermis hypoplasia (G11.000x005) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being
Congenital cerebellar ataxia with bilateral palsy (G11.000x004) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction
Congenital cerebellar ataxia (G11.000x003) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Cerebellar hypoplasia/aplasia (G11.000x002) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Congenital non-progressive ataxia (G11.000) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Huntington disease dementia is progressive subcortical cognitive decline in Huntington disease, with chorea/psychiatric symptoms; no cure, supportive/symptomatic.
神经内科Congenital chorea (G10.x00x005) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Benign non-progressive familial chorea (G10.x00x004) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being c
Huntington disease is autosomal dominant CAG-trinucleotide neurodegenerative chorea, cognitive decline, and psychiatric disturbance in mid-adulthood; no cure, supportive/symptomatic.
神经内科Sequelae of infectious-toxic encephalopathy (G09.x01) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being
Sequelae of CNS infectious disease (G09.x00x005) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compi
Sequelae of encephalomyelitis (G09.x00x004) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Sequelae of meningitis (G09.x00x003) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Sequelae of encephalitis are residual neurologic/cognitive/behavioral deficits after encephalitis: epilepsy/paresis/cognitive impairment; treat by supportive care, rehab, antiepileptics.
神经内科
|
