Hyperphosphatemia

Symptom Information:

Symptom ID: HPO:0002905
Synonyms:
Hyperphosphtemia [Orphanet:49320]
HYPERPHOSPHATAEMIA [HPO:0002905]
Serum phosphate increased [Orphanet:49320]
Hyperphosphatemia [OMIM:Hyperphosphatemia]
Blood phosphorus increased [MedDRA:10050196]
Blood phosphate increased [MedDRA:10050196]
Phosphate high [MedDRA:10050196]
Phosphate increased [MedDRA:10050196]
Plasma phosphate increased [MedDRA:10050196]
Serum inorganic phosphate increased [MedDRA:10050196]
Serum phosphate increased [MedDRA:10050196]
Hyperphosphataemia [MedDRA:10020711]
Quality:
Cross references:
Orphanet:49320 "Hyperphosphtemia" [Orphanet:49320]
OMIM: "Hyperphosphatemia" [OMIM:Hyperphosphatemia]
UMLS:C0085681 "HYPERPHOSPHATAEMIA" [HPO:0002905]
UMLS:C0553706 "Serum phosphate increased" [Orphanet:49320]
Is a (Direct Parents):
HPO         Abnormality of phosphate homeostasis
MedDRA Mineral and electrolyte analyses
Orphanet Abnormality of calcium-phosphate metabolism
MedDRA Phosphorus metabolism disorders
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)
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)