Hypercalcemia

Symptom Information:

Symptom ID: HPO:0003072
Synonyms:
Hypercalcaemia [HPO:0003072]
Hypercalcemia (disorder) [Orphanet:49220]
HYPERCALCAEMIA [HPO:0003072]
Serum calcium increased [Orphanet:49220]
Hypercalcemia [Orphanet:49220]
Hypercalcemia [OMIM:Hypercalcemia]
Hypercalcaemia [Orphanet:49220]
Blood calcium increased [Orphanet:49220]
Hypercalcaemia [MedDRA:10020583]
Calcium repletion serum [MedDRA:10020583]
Hypercalcemia [MedDRA:10020583]
Hypercalcaemia aggravated [MedDRA:10020583]
Hypercalcemia aggravated [MedDRA:10020583]
Blood calcium increased [MedDRA:10005396]
Ca increase [MedDRA:10005396]
Ca++ increased [MedDRA:10005396]
Calcium blood increased [MedDRA:10005396]
Calcium high [MedDRA:10005396]
Calcium increased [MedDRA:10005396]
Calcium increased serum [MedDRA:10005396]
Calcium total increased [MedDRA:10005396]
Plasma calcium increased [MedDRA:10005396]
Serum calcium increased [MedDRA:10005396]
Increased serum calcium [OMIM:Increased serum calcium]
Quality:
Cross references:
Orphanet:49220 "Hypercalcemia" [Orphanet:49220]
OMIM: "Hypercalcemia" [OMIM:Hypercalcemia]
OMIM: "Increased serum calcium" [OMIM:Increased serum calcium]
UMLS:C0020437 "HYPERCALCAEMIA" [HPO:0003072]
UMLS:C0595928 "Serum calcium increased" [Orphanet:49220]
UMLS:C0020437 "Hypercalcemia" [Orphanet:49220]
Is a (Direct Parents):
Orphanet Abnormality of calcium-phosphate metabolism
MedDRA Hyperparathyroid disorders
MedDRA Mineral and electrolyte analyses
HPO         Abnormality of calcium homeostasis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of ion homeostasis(HPO:0003111)
             Abnormality of cation homeostasis(HPO:0010929)
                Abnormality of divalent inorganic cation homeostasis(HPO:0010927)
                   Abnormality of calcium homeostasis(HPO:0004363)
                      Hypercalcemia(HPO:0003072)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Parathyroid gland disorders(MedDRA:10033949)
       Hyperparathyroid disorders(MedDRA:10020704)
          Hypercalcemia(HPO:0003072)
Investigations(MedDRA:10022891)
    Water, electrolyte and mineral investigations(MedDRA:10047843)
       Mineral and electrolyte analyses(MedDRA:10027637)
          Hypercalcemia(HPO:0003072)
Database Frequency: 36 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive infantile hypercalcemia (Orphanet:300547)
Blue diaper syndrome (Orphanet:94086)
Cushing syndrome (Orphanet:553)
Cutaneous mastocytosis (Orphanet:66646)
Diffuse neonatal hemangiomatosis (Orphanet:2123)
Familial hypocalciuric hypercalcemia (Orphanet:405)
Familial hypocalciuric hypercalcemia type 1 (Orphanet:93372)
Familial hypocalciuric hypercalcemia type 2 (Orphanet:101049)
Familial hypocalciuric hypercalcemia type 3 (Orphanet:101050)
Familial parathyroid adenoma (Orphanet:99877)
HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA (OMIM:239199)
HYPERVITAMINOSIS A, SUSCEPTIBILITY TO (OMIM:240150)
HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM (OMIM:612089)
Hyperparathyroidism - jaw tumor syndrome (Orphanet:99880)
Hypophosphatasia (Orphanet:436)
IMAGe syndrome (Orphanet:85173)
Infantile hypophosphatasia (Orphanet:247651)
Infantile myofibromatosis (Orphanet:2591)
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome (Orphanet:369837)
MOVED TO 614732 (OMIM:300290)
Mastocytosis (Orphanet:98292)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
Metaphyseal chondrodysplasia, Schmid type (Orphanet:174)
Multiple endocrine neoplasia type 1 (Orphanet:652)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Neonatal severe primary hyperparathyroidism (Orphanet:417)
Nephropathy - deafness - hyperparathyroidism (Orphanet:2668)
PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME (OMIM:171420)
PHEOCHROMOCYTOMAPHEOCHROMOCYTOMA, SUSCEPTIBILITY TO (OMIM:171300)
Parathyroid carcinoma (Orphanet:143)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Rhabdoid tumor (Orphanet:69077)
Sarcoidosis (Orphanet:797)
Small cell carcinoma of the bladder (Orphanet:284400)
Ulna metaphyseal dysplasia syndrome (Orphanet:1837)
Williams syndrome (Orphanet:904)