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60 results

• Condition
  Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1, Susceptibility To
  Topicphenotype HERBHBDIS023367
  phenotype
• Condition
  Amyotrophic Lateral Sclerosis, Guam Form
  Topicsyndrome OMIM105500 MeSHD000690 HERBHBDIS010040
  disease · Nervous System Diseases; Nutritional and Metabolic Diseases
• Condition
  Anomalous Atrioventricular Excitation
  Topicphenotype HERBHBDIS028481
  phenotype · Cardiovascular Diseases; Pathological Conditions, Signs and Symptoms
• Condition
  Atherosclerotic Parkinsonism
  Topicsyndrome MeSHD010302 HERBHBDIS011287
  disease · Nervous System Diseases
• Condition
  Atypical Juvenile Parkinsonism
  Topicsyndrome HERBHBDIS026769
  disease
• Condition
  Atypical Parkinson Disease
  Topicsyndrome OMIM168601 MeSHC566823 HERBHBDIS018457
  disease · Nervous System Diseases
• Condition
  Atypical Parkinsonism
  Topicsyndrome HERBHBDIS026119
  disease · Nervous System Diseases
• Condition
  Autosomal Dominant Juvenile Parkinson Disease
  Topicsyndrome MeSHD020734 HERBHBDIS011535
  disease · Nervous System Diseases
• Condition
  Autosomal Dominant Late Onset Parkinson Disease
  Topicsyndrome HERBHBDIS025910
  disease · Nervous System Diseases
• Condition
  Autosomal Dominant Parkinsonism
  Topicsyndrome MeSHD020734 HERBHBDIS011536
  disease · Nervous System Diseases
• Condition
  Autosomal Recessive Parkinsonism
  Topicsyndrome MeSHD020734 HERBHBDIS011537
  disease · Nervous System Diseases
• Condition
  Dementia Due To Parkinson'S Disease
  Topicdisease HERBHBDIS028326
  disease · Nervous System Diseases
• Condition
  Dementia In Parkinson'S Disease
  Topicsyndrome ICD-10F02.3 HERBHBDIS008449
  disease
• Condition
  Dystonia 3, Torsion, X-Linked
  Topicsyndrome OMIM314250 MeSHC564048 HERBHBDIS015730
  disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
• Condition
  Dystonia Musculorum Deformans
  Topicsyndrome HPOHP:0001304 MeSHD004422 HERBHBDIS000864
  disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
• Condition
  End Stage Parkinson'S Disease
  Topicsyndrome HERBHBDIS025348
  disease
• Condition
  Familial Juvenile Parkinsonism
  Topicsyndrome MeSHD020734 HERBHBDIS011539
  disease · Nervous System Diseases
• Condition
  Familial Torsion Dystonia
  Topicsyndrome HERBHBDIS020076
  disease
• Condition
  Hemiparkinsonism
  Topicsyndrome HERBHBDIS014158
  disease
• Condition
  Idiopathic Familial Dystonia
  Topicsyndrome ICD-10G24.1 MeSHD020821 HERBHBDIS008681
  disease · Nervous System Diseases
• Condition
  Idiopathic Parkinsonism Or Parkinson'S Disease
  Topicsyndrome HERBHBDIS012237
  disease
• Condition
  Lown-Ganong-Levine Syndrome
  Topicsyndrome MeSHD008151 HERBHBDIS001781
  disease · Cardiovascular Diseases
• Condition
  Mitochondrial Complex I Deficiency, Mitochondrial Type 3 (Finding)
  Topicphenotype OMIM516000 HERBHBDIS030100
  phenotype
• Condition
  Mixed Dementia; And Dementia Related To Stroke, Parkinson'S Or Creutzfeldt-Jakob Diseases); Frontotemporal Dementia Such As Pick'S Disease; Non-Alzheimer'S Dementia (E.G., Lewy Body Dementia, Vascular Or Multi-Infarct Dementia
  Topicdisease HERBHBDIS027040
  disease
• Condition
  Parkinson Disease
  Topicsyndrome OMIM516000 ICD-10G20 MeSHD010300 HERBHBDIS002313
  disease · Nervous System Diseases
• Condition
  Parkinson Disease 1, Autosomal Dominant (Disorder)
  Topicsyndrome OMIM168601 HERBHBDIS018456
  disease
• Condition
  Parkinson Disease 10
  Topicsyndrome OMIM606852 MeSHC564653 HERBHBDIS016380
  disease · Nervous System Diseases
• Condition
  Parkinson Disease 11, Autosomal Dominant, Susceptibility To
  Topicphenotype OMIM607688 HERBHBDIS025539
  phenotype
• Condition
  Parkinson Disease 12
  Topicsyndrome OMIM300557 MeSHC564486 HERBHBDIS016192
  disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
• Condition
  Parkinson Disease 13, Autosomal Dominant, Susceptibility To
  Topicdisease OMIM610297 HERBHBDIS028909
  disease
• Condition
  Parkinson Disease 14, Autosomal Recessive
  Topicsyndrome OMIM612953 MeSHC567844 HERBHBDIS019980
  disease · Nervous System Diseases
• Condition
  Parkinson Disease 15, Autosomal Recessive (Disorder)
  Topicsyndrome OMIM260300 MeSHC538104 HERBHBDIS016676
  disease · Eye Diseases; Nervous System Diseases
• Condition
  Parkinson Disease 16 (Disorder)
  Topicsyndrome OMIM613164 MeSHC567726 HERBHBDIS019904
  disease · Nervous System Diseases
• Condition
  Parkinson Disease 17
  Topicsyndrome OMIM614203 HERBHBDIS021270
  disease
• Condition
  Parkinson Disease 18
  Topicsyndrome OMIM614251 HERBHBDIS021282
  disease
• Condition
  Parkinson Disease 19A, Juvenile-Onset
  Topicsyndrome OMIM615528 HERBHBDIS022377
  disease
• Condition
  Parkinson Disease 19B, Early-Onset
  Topicsyndrome OMIM615528 HERBHBDIS026354
  disease
• Condition
  Parkinson Disease 2, Autosomal Recessive Juvenile
  Topicsyndrome OMIM600116 MeSHD020734 HERBHBDIS018467
  disease · Nervous System Diseases
• Condition
  Parkinson Disease 20, Early-Onset
  Topicsyndrome OMIM615530 HERBHBDIS029500
  disease
• Condition
  Parkinson Disease 22, Autosomal Dominant
  Topicsyndrome OMIM616710 HERBHBDIS029843
  disease
• Condition
  Parkinson Disease 23, Autosomal Recessive Early-Onset
  Topicsyndrome OMIM616840 HERBHBDIS025632
  disease
• Condition
  Parkinson Disease 4, Autosomal Dominant Lewy Body (Disorder)
  Topicsyndrome OMIM605543 MeSHC565324 HERBHBDIS017019
  disease · Mental Disorders; Nervous System Diseases
• Condition
  Parkinson Disease 5, Autosomal Dominant
  Topicsyndrome OMIM613643 HERBHBDIS020701
  disease
• Condition
  Parkinson Disease 6, Autosomal Recessive Early-Onset
  Topicsyndrome OMIM605909 MeSHC565276 HERBHBDIS016990
  disease · Nervous System Diseases
• Condition
  Parkinson Disease 6, Late-Onset, Susceptibility To
  Topicphenotype OMIM605909 HERBHBDIS018800
  phenotype
• Condition
  Parkinson Disease 7, Autosomal Recessive Early-Onset
  Topicsyndrome OMIM606324 MeSHC565238 HERBHBDIS016956
  disease · Nervous System Diseases
• Condition
  Parkinson Disease 8 (Disorder)
  Topicsyndrome OMIM607060 HERBHBDIS016360
  disease
• Condition
  Parkinson Disease, Familial, Type 1
  Topicsyndrome MeSHC566823 HERBHBDIS021455
  disease · Nervous System Diseases
• Condition
  Parkinson Disease, Late-Onset
  Topicsyndrome OMIM168600 HERBHBDIS020869
  disease
• Condition
  Parkinson Disease, Mitochondrial (Disorder)
  Topicsyndrome OMIM556500 MeSHC564015 HERBHBDIS015718
  disease · Nervous System Diseases; Nutritional and Metabolic Diseases
• Condition
  Parkinson Disease, Postencephalitic
  Topicsyndrome ICD-10G21.3 MeSHD010301 HERBHBDIS002314
  disease · Nervous System Diseases
• Condition
  Parkinson Disease, Secondary Vascular
  Topicsyndrome MeSHD010302 HERBHBDIS011286
  disease · Nervous System Diseases
• Condition
  Parkinson's disease
  Topicdisease
• Condition
  Parkinson'S Disease And Parkinsonism
  Topicsyndrome HERBHBDIS012466
  disease
• Condition
  Parkinson'S Disease Psychosis
  Topicdisease HERBHBDIS022159
  disease
• Condition
  Parkinsonian Disorders
  Topicgroup HPOHP:0001300 MeSHD020734 HERBHBDIS005423
  group · Nervous System Diseases
• Condition
  Parkinsonian symptoms
  Topicdisease
• Condition
  Parkinsonian Tremor
  Topicphenotype HPOHP:0002322 HERBHBDIS010385
  phenotype · Nervous System Diseases; Pathological Conditions, Signs and Symptoms
• Condition
  Parkinsonism Or Parkinson'S Disease Nos
  Topicsyndrome HERBHBDIS012236
  disease
• Condition
  Parkinsonism With Favorable Response To Dopaminergic Medication
  Topicphenotype HPOHP:0002548 HERBHBDIS016362
  phenotype · Nervous System Diseases