Familial hypoparathyroidism with pernicious anemia, steatorrhea and adrenocortical insufficiency: a variant of mucoviscidosis.
D000302:Adrenal Cortex; D000303:Adrenal Cortex Diseases; D000740:Anemia; D000752:Anemia, Pernicious; D002446:Celiac Disease; D002648:Child; D003550:Cystic Fibrosis / Q000235:genetics*; D004194:Disease; D006801:Humans; D007011:Hypoparathyroidism; D007223:Infant; D010279:Parathyroid Diseases; D010280:Parathyroid Glands; D045602:Steatorrhea
ADRENAL CORTEX/diseases; ANEMIA, PERNICIOUS/in infancy and childhood; PANCREATIC CYSTIC FIBROSIS/genetics; PARATHYROID GLANDS/diseases; SPRUE/in infancy and childhood