Multiple Endocrine Neoplasia Type 2A

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Annotated Information

Classification and Resources

ID 122
ICD-10 ICD10CM:D44.8;
ICD-9-CM
OMIM OMIM:171400;
SNOMED-CT
Orphanet
MeSH MSH:D018813;
DO

Defination

An autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis.

Synonyms

MEN2A  ; multiple endocrine neoplasia II  ; Sipple syndrome  ;

Etiology

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Diagnosis

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Symptoms

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Treatment

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Labs working on this disease

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References

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