has material basis in germline mutation in NR0B1 X-linked disease congenital nervous system disorder X-linked adrenal hypoplasia congenita https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/adrenal_hypoplasia_congenital cytomegalic congenital adrenal hypoplasia UMLS:C0342482 X-linked AHC adrenal hypoplasia congenita AHC Addison disease, X-linked NANDO:1200403 A X-linked condition characterized by underdevelopment of the adrenal gland and adrenal insufficiency caused by mutation(s) in the NR0B1 gene, resulting in decreased activity of the nuclear receptor protein DAX1, which may be associated with hypogonadotropic hypogonadism. AHC with HHG Orphanet:95702 OMIM:300200 MONDO:0010264 adrenal hypoplasia, congenital mineralocorticoid deficiency, isolated cytomegalic adrenocortical hypoplasia adrenal hypoplasia, congenital, with precocious puberty adrenal insufficiency, progressive, and hypogonadotropic hypogonadism DOID:0080156 NCIT:C123725 adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism GARD:0000555 AHC with isolated gonadotropin deficiency X-linked adrenal hypoplasia congenita MEDGEN:87442 X-linked congenital adrenal hypoplasia SCTID:93235007 adrenal hypoplasia, congenital, X-linked recessive NANDO:2200357 chronic primary adrenal insufficiency congenital hypogonadotropic hypogonadism alternating hemiplegia of childhood