Hyperparathyroidism
Symptom Information:
Symptom ID: | HPO:0000843 | ||||||
Synonyms: |
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Quality: | |||||||
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 the endocrine system(HPO:0000818) Abnormality of the parathyroid gland(HPO:0000828) Abnormality of the parathyroid physiology(HPO:0011767) Hyperparathyroidism(HPO:0000843) MedDRA: Endocrine disorders(MedDRA:10014698) Parathyroid gland disorders(MedDRA:10033949) Hyperparathyroid disorders(MedDRA:10020704) Hyperparathyroidism(HPO:0000843) |
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Database Frequency: | 17 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Familial hypocalciuric hypercalcemia | (Orphanet:405) |
Familial visceral myopathy | (Orphanet:2604) |
Fibrous dysplasia of bone | (Orphanet:249) |
HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA | (OMIM:239199) |
HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM | (OMIM:612089) |
Hyperparathyroidism - jaw tumor syndrome | (Orphanet:99880) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
McCune-Albright syndrome | (Orphanet:562) |
Multiple endocrine neoplasia type 1 | (Orphanet:652) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Multiple endocrine neoplasia type 2A | (Orphanet:247698) |
Neonatal severe primary hyperparathyroidism | (Orphanet:417) |
Nephropathy - deafness - hyperparathyroidism | (Orphanet:2668) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Parathyroid carcinoma | (Orphanet:143) |
Pendred syndrome | (Orphanet:705) |
Polyostotic fibrous dysplasia | (Orphanet:93276) |