Abnormality of calcium-phosphate metabolism
Symptom Information:
| Symptom ID: | HPO:0100530 | ||||
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HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of calcium-phosphate metabolism(HPO:0100530) MedDRA: |
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| Database Frequency: | 12 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Albright hereditary osteodystrophy | (Orphanet:665) |
| Amelogenesis imperfecta - nephrocalcinosis | (Orphanet:1031) |
| Autoimmune polyendocrinopathy type 1 | (Orphanet:3453) |
| Familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement | (Orphanet:2196) |
| Familial isolated hypoparathyroidism | (Orphanet:2238) |
| Familial isolated hypoparathyroidism due to agenesis of parathyroid gland | (Orphanet:2239) |
| Hypophosphatemic rickets | (Orphanet:437) |
| Metaphyseal chondrodysplasia, Jansen type | (Orphanet:33067) |
| Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
| Microlissencephaly - micromelia | (Orphanet:50810) |
| Neonatal severe primary hyperparathyroidism | (Orphanet:417) |
| Oculocerebrorenal syndrome | (Orphanet:534) |