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
Also Known As:
Hypoadrenocorticism, Familial; AHC with Isolated Gonadotropin Deficiency; Addison Disease, X-Linked; Adrenal Hypoplasia, Congenital; Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism; Complex Glycerol Kinase Deficiency; Cytomegalic Adrenocortical Hypoplasia; Familial X-linked Addison Disease; X-linked Adrenal Hypoplasia; X-linked Congenital Adrenal Hypoplasia; Xp21 Contiguous Gene Deletion Syndrome; Addison Disease, X Linked; Adrenal Hypoplasia, X-linked; Congenital Adrenal Hypoplasia; Congenital Adrenal Hypoplasias; Cytomegalic Adrenocortical Hypoplasias; Familial Hypoadrenocorticisms; Familial X linked Addison Disease; Hypoadrenocorticisms, Familial; Hypoplasia, Congenital Adrenal; X linked Adrenal Hypoplasia; X linked Congenital Adrenal Hypoplasia; X-Linked Addison Disease