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MeSH 搜索器

Hypoadrenocorticism, Familial

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
推出的年份: 2018(2010)
副标题
树号: C19.053.500.263.500
MeSH 单一 ID: D000075262
进入的组:
  • Familial Hypoadrenocorticism
  • Familial Hypoadrenocorticisms
  • Hypoadrenocorticisms, Familial
  • Complex Glycerol Kinase Deficiency
  • Xp21 Contiguous Gene Deletion Syndrome
  • X-linked Adrenal Hypoplasia
  • Adrenal Hypoplasia, X-linked
  • X linked Adrenal Hypoplasia
  • Familial X-linked Addison Disease
  • Familial X linked Addison Disease
  • Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism
  • Addison Disease, X-Linked
  • Addison Disease, X Linked
  • X-Linked Addison Disease
  • Cytomegalic Adrenocortical Hypoplasia
  • Cytomegalic Adrenocortical Hypoplasias
  • AHC with Isolated Gonadotropin Deficiency
  • X-linked Congenital Adrenal Hypoplasia
  • X linked Congenital Adrenal Hypoplasia
  • Adrenal Hypoplasia, Congenital
  • Congenital Adrenal Hypoplasia
  • Congenital Adrenal Hypoplasias
  • Hypoplasia, Congenital Adrenal

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