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- Disease Information
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Disease Processes ▼
- Auto Immune
- Vascular-Arteriosclerosis
- Biochemical
- Congenital-developmental
- Deficiency
- Degenrative-Necrosis
- Electromagnetic-Physics
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- Hereditofamilial
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- Idiopathic
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- Infectious agent
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- Trauma
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Major Organs-Systems ▼
- Systemic
- Pediatric
- Nervous & Sensory System (Neurology)
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- Respiratory (Pulmonary) System
- Gastro-Intestinal (Digestive) System
- Urinary System
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- Musculoskeletal System
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- Tissue/Cells/Organelles
Disease Comparison Results (show all mode) for Hemoglobin E thalassemia and Huntington's chorea
Found: 161 | Differences: 155
Found: 33 | Differences: 27
Hemoglobin E thalassemia and Huntington's chorea sharing 6 common findings. (show all, show common, show differences)
- Clinical Manifestations
- Signs & Symptoms
- Akinetic rigid frozen Posture
- Dysphagia for solids
- Dysphagia Liquids
- Failure to Thrive
- Rigidity/Muscle/movement
- Tongue movements/involuntary
- Muscle stiffness/rigidity
- Abnormal movements/involuntary
- Action Tremor
- Akinesia/poor voluntary movement
- Apathy/Indifference
- Apraxia/dyspraxia
- Ataxia
- Ataxia, Cerebellar type
- Ataxia/Motor tremor type
- Athetosis
- Basal ganglion signs
- Behavior problems
- Chorea signs
- Choreoathetoid movement
- Choreoathetosis
- Clonus/bilateral ankle (sustained)
- CNS symptoms/signs
- Cognitive defect
- Confabulation
- Confusion/Disoriented
- Coordination/signs
- Delirium
- Difficulty concentrating/Distraction/Forgetful
- Dysarthria
- Dystonia
- Dystonia, acquired
- Equinus Posture/Ankles
- Executive function loss/apathy/inertia
- Extrapyramidal signs
- Finger to nose test abnormality
- Gait disturbance/abnormality
- Handwriting progressive decline
- Hyperkinetic Movement Disorder
- Impaired judgement/signs
- Inattention
- Involuntary movements
- Irritability/short tempered
- Mental Slowing Deteriation
- Motor slowing
- Movement or gait disorder/signs
- Myoclonus/Myoclonic jerks on exam
- Near recall/memory deficit/defect
- Odd body posturing
- Personality change
- Rapidly progressive dementia
- Slow speech
- Spasticity/Spastic gait
- Staggering Gait
- Tics/sign
- Tremor
- Tremor in Elderly
- Tremor,coarse
- Tremor,intention
- Tremor,resting
- Unable to tandem walk/straight line
- Peculiar respiratory/grunts noises
- Depressed/discouraged/sad
- Destructive Behavior
- Mood swings/changes
- Personality changes/gradual
- Psychiatric manifestations/problems/difficulties
- Volatility/wild mood swings
- Withdrawn Unresponsive
- Difficulty Talking
- Listlessness/lassitude
- Restlessness/Anxiousness
- Walking difficulties
- Clinical Presentation & Variations
- Presentation/Movement Disorder Ataxia Dementia Progressive
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
- Course/Progressive/slowly chronic illness
- Course/Twenty years survival/from onset
- Onset/fourth decade
- Onset/gradual
- Demographics & Risk Factors
- Population Group
- Child
- Population/Pediatrics population
- Family History
- Family history/Dementia
- Family history/Gait disorders
- Family history/Nerve disease
- Family history/Tremor
- Event, Activity, Behavioral & Seasonal Factors
- Lifestyle/Antisocial/acting-out behavior
- Sex & Age Groups
- Population/Adult/all
- Population/Forties adult
- Population/Thirties adult
- Laboratory Tests
- Microbiology & Serology Findings
- Microlab/PCR identification
- Abnormal Lab Findings (Non Measured)
- Chromosomal abnormality (Lab)
- DNATest specific/genetics laboratory/abnormality (Lab)
- Abnormal Lab Findings - Decreased
- Isoleucine (Lab)
- Leucine (Lab)
- Tyrosine (Lab)
- Valine (Lab)
- Zinc, serum (Lab)
- Abnormal Lab Findings - Increased
- Free fatty acids/FFA/Non-esterified (Lab)
- Total Protein, serum (Lab)
- URINE Norepinephrine
- Diagnostic Test Results
- Pathology
- PATH/Brain abnormal
- CT Scan
- CT Scan/Head Boxcar ventricles pattern
- CT Scan/Head caudate nucleus lesion
- CT Scan/Head Cortical atrophy
- MRI/Head caudate nucleus atrophy
- PET Scan/Head Caudate Nucleus/Lack glucose uptake
- PET Scan/Head FDDNP abnormal
- Associated Diseases & Rule outs
- Associated Disease & Complications - Rule Outs
- Alzheimers disease
- Gilles de Tourette syndrome
- Tardive dyskinesia syndrome
- Associated Disease & Complications - Causes
- Amnesia
- Basal gangion lesion/secondary
- Dementia
- Dyskinesia
- Extrapyramidal disease/manifestation
- Huntingtons chorea
- Neurobehavior Problems
- Neurodevelopmental disorders
- Parkinsons disease
- Pneumonia, aspiration
- Psychosis
- Subdural hematoma
- Tuberculosis
- Tuberculosis, pulmonary
- Torticollis
- Akinetic Rigid Syndrome
- Ataxia Disorder
- Disease Mechanism & Classification
- Class
- CLASS/Basal ganglia lesion/involvement/disorders (ex)
- CLASS/Brain/CNS disorder (ex)
- CLASS/Neurologic (category)
- Pathophysiology
- Pathophysiology/Anticipation kindred inheritance earlier onset effect
- Pathophysiology/Chromosome 4/Unstable CAG repeat/4p
- Pathophysiology/Corpus striatum lesion/disorder
- Pathophysiology/Gene HD 143100 OMIM/locus 4p
- Pathophysiology/Gene locus 11p11.2
- Pathophysiology/Gene Locus Identified/OMIM database
- Pathophysiology/Gene locus/Chromosome 4
- Pathophysiology/Genomic base pair repeats mutation
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Pathophysiology/Hereditary anticipation/generations worsen
- Pathophysiology/Hereditary disease/Adult manifestations
- Pathophysiology/Single gene locus indentified
- Pathophysiology/Caudate nucleus lesion/effect
- Pathophysiology/CNS degeneration
- Pathophysiology/Neurologic degenerative disorder (ex)
- Process
- PROCESS/Autosomal dominant hereditary disease (ex).
- PROCESS/Eponymic (category)
- PROCESS/Hereditofamilial (category)
- PROCESS/Movement disorder (ex)
- PROCESS/Use/Age/atrophic disorder (category)
- PROCESS/Developmental degenerative neurological disorder (ex)
- PROCESS/Hereditary ataxia disorder (ex)
- PROCESS/Hyperkinetic Movement disorders
- Treatment
- Drug Therapy
- RX/No effective/definitive treatment yet available
- Other Treatments
- TX/Genetic counselling
- Clinical Manifestations
- Clinical Presentation & Variations
- Anemia in Children
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
- Demographics & Risk Factors
- Past History
- Past history/Anemia
- Past history/Refractory anemia
- Population Group
- Child
- Population/Pediatrics population
- Family History
- Family history/Anemia
- Sex & Age Groups
- Population/Child
- Population/Child-Infant Only
- Population/Children/all
- Laboratory Tests
- Abnormal Lab Findings (Non Measured)
- Hemoglobin electrophoresis abnormal (Lab)
- Microcytes/small RBCs on Blood smear
- Microcytosis/microcytic anemia (Lab)
- Normocytic anemia
- Normocytic Anemia/High Retic count
- Normocytic/Normochromic Anemia (Lab)
- Abnormal Lab Findings - Decreased
- Hematocrit (Lab)
- Hemoglobin (Lab)
- MCV/Mean Corpuscular Volume (Lab)
- RBC/Red Blood Count (Lab)
- Abnormal Lab Findings - Increased
- Fetal hemoglobin (Lab)
- Iron, serum (Lab)
- Diagnostic Test Results
- Pathology
- Bone Marrow/Iron stores normal/anemia
- Bone Marrow/Iron stores/increased
- Associated Diseases & Rule outs
- Associated Disease & Complications - Rule Outs
- Iron deficiency anemia
- Paroxysmal cold hemoglobinuria
- Associated Disease & Complications - Causes
- Anemia
- Disease Mechanism & Classification
- Class
- CLASS/Hematologic (category)
- Pathophysiology
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Process
- PROCESS/Hereditofamilial (category)
- PROCESS/Hemoglobinopathy disorder (ex)
- PROCESS/Molecular/hematologic disorder (ex)