adrenal gland disorder adrenomyodystrophy https://www.malacards.org/card/adrenomyodystrophy MESH:C538051 UMLS:C1846044 Orphanet:977 GARD:0000562 icd11.foundation:46666832 MONDO:0010288 SCTID:763311001 MEDGEN:337494 adrenomyodystrophy OMIM:300270 Adrenomyodystrophy is an extremely rare genetic endocrine disease characterized by primary adrenal insufficiency, dystrophic myopathy, hepatic steatosis, severe psychomotor delay, megalocornea, failure to thrive, chronic constipation, and terminal bladder ectasia which can lead to death. There have been no further descriptions in the literature since 1982. chronic primary adrenal insufficiency