Autoimmune Polyendocrine Syndrome Type 1

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Annotated Information

Classification and Resources

ID 58
ICD-10
ICD-9-CM
OMIM
SNOMED-CT
Orphanet
MeSH
DO

Defination

An autoimmune polyendocrine syndrome that is inherited in an autosomal recessive fashion, which is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs.

Synonyms

autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy  ; Autoimmune Polyglandular Syndrome I  ; Whitaker syndrom  ;

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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