Renal phosphate wasting
Symptom Information:
Symptom ID: | HPO:0000117 | ||||||||||
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 the genitourinary system(HPO:0000119) Abnormality of the urinary system(HPO:0000079) Abnormality of the urinary system physiology(HPO:0011277) Abnormality of urine homeostasis(HPO:0003110) Abnormal urinary electrolyte concentration(HPO:0012591) Abnormal urine phosphate concentration(HPO:0012599) Renal phosphate wasting(HPO:0000117) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of urine homeostasis(HPO:0003110) Abnormal urinary electrolyte concentration(HPO:0012591) Abnormal urine phosphate concentration(HPO:0012599) Renal phosphate wasting(HPO:0000117) MedDRA: |
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Database Frequency: | 14 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant hypophosphatemic rickets | (Orphanet:89937) |
Dent disease type 1 | (Orphanet:93622) |
Dominant hypophosphatemia with nephrolithiasis or osteoporosis | (Orphanet:244305) |
FANCONI RENOTUBULAR SYNDROME 2 | (OMIM:613388) |
FANCONI RENOTUBULAR SYNDROME 3 | (OMIM:615605) |
HYPOPHOSPHATEMIA, RENAL, WITH INTRACEREBRAL CALCIFICATIONS | (OMIM:241519) |
HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM | (OMIM:612089) |
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE | (OMIM:300554) |
Hereditary hypophosphatemic rickets with hypercalciuria | (Orphanet:157215) |
NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1 | (OMIM:612286) |
NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2 | (OMIM:612287) |
Opsismodysplasia | (Orphanet:2746) |
Primary Fanconi syndrome | (Orphanet:3337) |
X-linked hypophosphatemia | (Orphanet:89936) |