FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term familial hypocalciuric hypercalcemia ID (Ontology) DOID:0060699 (Human Disease)
Definition A hypercalcemia characterized by autosomal dominant inheritance with elevation of serum calcium levels and decreased urinary calcium excretion.
Also Known As "familial benign hypercalcemia" ; "familial benign hypocalciuric hypercalcemia" ; "FBH" (for all, see Synonyms field below)
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Spanning Tree (Parents/Children)
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disease of metabolism
 |__inherited metabolic disorder__
autosomal genetic disease         |
 |__autosomal dominant disease____|
calcium metabolism disease        |
 |__hypercalcemia_________________|
genetic disease                   |
 |__inherited metabolic disorder__|
                                  familial hypocalciuric hypercalcemia  2 rec.
                                   |__familial hypocalciuric hypercalcemia 1
                                   |__familial hypocalciuric hypercalcemia 2 1 rec.
                                   |__familial hypocalciuric hypercalcemia 3 1 rec.
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Is a autosomal dominant disease
hypercalcemia
inherited metabolic disorder
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Synonyms
  • "familial benign hypercalcemia" EXACT
    "familial benign hypocalciuric hypercalcemia" EXACT
    "FBH" EXACT OMO:0003012
    "FBHH" EXACT OMO:0003012
    "FHH" EXACT OMO:0003012
Secondary IDs
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GARD:10828
ICD10CM:E83.5
MIM:PS145980
ORDO:405