ZFIN Human Disease: familial hypocalciuric hypercalcemia

OBO ID: DOID:0060699

Term Name:	familial hypocalciuric hypercalcemia		Search Ontology:
Synonyms:	familial benign hypercalcemia familial benign hypocalciuric hypercalcemia FBH FBHH FHH
Definition:	A hypercalcemia characterized by autosomal dominant inheritance with elevation of serum calcium levels and decreased urinary calcium excretion. https://www.ncbi.nlm.nih.gov/pubmed/19809483
References:	GARD:10828 ICD10CM:E83.5 OMIM:PS145980 ORDO:405
Ontology:	Human Disease ( DOID:0060699 )

Relationships

is a type of:	autosomal dominant disease hypercalcemia inherited metabolic disorder autosomal dominant disease hypercalcemia inherited metabolic disorder Show first 5 Terms
has subtype:	familial hypocalciuric hypercalcemia 1 familial hypocalciuric hypercalcemia 2 familial hypocalciuric hypercalcemia 3 familial hypocalciuric hypercalcemia 1 familial hypocalciuric hypercalcemia 2 familial hypocalciuric hypercalcemia 3 Show first 5 Terms

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Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None