disease has basis in disruption of disease caused by disruption of parathyroid hormone secretion hereditary hypoparathyroidism familial hypoparathyroidism https://www.malacards.org/card/familial_isolated_hypoparathyroidism hypoparathyroidism, familial isolated MONDO:0016390 familial isolated hypoparathyroidism NORD:1128 OMIMPS:146200 GARD:0002910 Familial Isolated Hypoparathyroidism MESH:C537156 A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism due to deficient secretion of parathormone (PTH), without other endocrine disorders or developmental defects. MEDGEN:322005 icd11.foundation:1907423603 DOID:0111387 hypoparathyroidism, familial UMLS:C1832648 hypoparathyroidism familial isolated SCTID:725036000 Orphanet:2238 inborn errors of metabolism obsolete metabolic disease with cataract