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Begreppsinformation

Immune System Diseases > Autoimmune Diseases > Addison Disease > Hypoadrenocorticism, Familial
Endocrine System Diseases > Adrenal Gland Diseases > Adrenal Insufficiency > Addison Disease > Hypoadrenocorticism, Familial

Föredragen term

Hypoadrenocorticism, Familial  

Typ

  • Topical Descriptor

Överordnat begrepp

Hänvisningstermer

  • Adrenal Hypoplasia, X-linked
  • Complex Glycerol Kinase Deficiency
  • X linked Adrenal Hypoplasia
  • X-linked Adrenal Hypoplasia
  • Xp21 Contiguous Gene Deletion Syndrome

Användningsanmärkning

  • Hereditary forms of Addison disease that may exhibit autosomal recessive or X-linked inheritance. They are characterized by severe neurological symptoms, APNEA; and death in infancy. OMIM: 240200

Anmärkning om ändringshistoria

  • 2018(2010)

Termer på andra språk

URI

http://www.yso.fi/onto/mesh/D000075262

Ladda ned detta begrepp:

RDF/XML TURTLE JSON-LD Skapad 2017-07-11, senast editerad 2024-06-25