Hyperphosphatemia
Symptom Information:
Symptom ID: | HPO:0002905 | ||||||||||||
Synonyms: |
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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 phosphate homeostasis(HPO:0100529) Hyperphosphatemia(HPO:0002905) MedDRA: Investigations(MedDRA:10022891) Water, electrolyte and mineral investigations(MedDRA:10047843) Mineral and electrolyte analyses(MedDRA:10027637) Hyperphosphatemia(HPO:0002905) Metabolism and nutrition disorders(MedDRA:10027433) Bone, calcium, magnesium and phosphorus metabolism disorders(MedDRA:10013296) Phosphorus metabolism disorders(MedDRA:10034941) Hyperphosphatemia(HPO:0002905) |
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Database Frequency: | 18 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Albright hereditary osteodystrophy | (Orphanet:665) |
Autosomal dominant hypocalcemia | (Orphanet:428) |
Familial isolated hypoparathyroidism due to impaired PTH secretion | (Orphanet:189466) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3 | (OMIM:614207) |
HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES | (OMIM:239350) |
Hypercalcemic tumoral calcinosis | (Orphanet:306661) |
Hypouricemia, renal, 2 | (OMIM:612076) |
Juvenile Paget disease | (Orphanet:2801) |
King-Denborough syndrome | (Orphanet:99741) |
MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2 | (OMIM:154275) |
MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3 | (OMIM:154276) |
Malignant hyperthermia | (Orphanet:423) |
Pseudohypoparathyroidism type 1A | (Orphanet:79443) |
Pseudohypoparathyroidism type 1B | (Orphanet:94089) |
Pseudohypoparathyroidism type 1C | (Orphanet:79444) |
Pseudohypoparathyroidism type 2 | (Orphanet:94090) |
Sanjad-Sakati syndrome | (Orphanet:2323) |
Tumoral calcinosis | (Orphanet:53715) |