Hypercalcemia
Symptom Information:
Symptom ID: | HPO:0003072 | ||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |