Disease Comparison Results (show all mode) for Endocrine adenomata, type 2 (MEA2) and Hemoglobin M disease

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Hemoglobin M disease

Found: 13 | Differences: 5

Endocrine adenomata, type 2 (MEA2)

Found: 51 | Differences: 43

Endocrine adenomata, type 2 (MEA2) and Hemoglobin M disease sharing 8 common findings. (show all, show common, show differences)

Clinical Manifestations
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Laboratory Tests
Abnormal Lab Findings (Non Measured)
Hemoglobin electrophoresis abnormal (Lab)
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)
Clinical Manifestations
Signs & Symptoms
Tall Adult
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Past History
Past history/Pheochromocytoma
Established Disease Population
Patient/Multiple/MEN2/endocrine adenomata
Population Group
Child
Population/Pediatrics population
Family History
Family history/Endocrine disorder
Family history/MEA/endocrine tumors
Family history/Pheochromocytoma
Sex & Age Groups
Population/Child
Population/Children/all
Laboratory Tests
Abnormal Lab Findings (Non Measured)
RET Oncogene Mutation
Chromosomal abnormality (Lab)
Diagnostic Test Results
Pathology
PATH/Parathyroid Hyperplasia
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Hyperparathyroidism, primary
Associated Disease & Complications - Causes
Endocrine adenomata, multiple, type 2/MEA II
Endocrine dysfunction
Hyperparathyroidism, primary
Multiple endocrine adenomata/hereditary
Pheochromocytoma
Thyroid Cancer
Thyroid malignancy/carcinoma
Thyroid medullary carcinoma
Disease Mechanism & Classification
Class
CLASS/Endocrine gland (category)
Pathophysiology
Pathophysiology/Gene locus 10q11.2
Pathophysiology/Gene locus Chromosome 10
Pathophysiology/Gene locus Chromosome 10q
Pathophysiology/Gene locus Chromosome 20
Pathophysiology/Gene locus Chromosome 20p
Pathophysiology/Gene locus Chromosome X.
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Gene locus Xq28
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Hereditary disease/Adult manifestations
Pathophysiology/Oncogene RET/Locus 10q
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Benign tumor (ex).
PROCESS/Endocrine/humoral disorders (category)
PROCESS/Hereditofamilial (category)
PROCESS/Hereditofamilial/tumor syndrome (ex)
PROCESS/Neoplastic (category)
PROCESS/Endocrine adenoma (ex).
PROCESS/Multiple endocrine neoplasia syndromes (ex)
Synonyms
Synonym
Synonym/MEN IIA/Sipples syndrome
Synonym/Multiple endocrine adenomata syndrome/MEN/II
Synonym/Pheochromocytoma/thyroid medullary ca
Synonym/PTC syndrome
Synonym/Sipple syndrome
Synonym/Thyroid medullary ca/pheochromocytoma synd
Treatment
Other Treatments
TX/Genetic counselling
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