Hyperparathyroidism

Symptom Information:

Symptom ID: HPO:0000843
Synonyms:
Hyperparathyroidsm [Orphanet:41330]
Hyperparathyroidism [OMIM:Hyperparathyroidism]
Hyperparathyroidy [Orphanet:41330]
Hyperparathyroidism [MedDRA:10020705]
Quality:
Cross references:
Orphanet:41330 "Hyperparathyroidy" [Orphanet:41330]
OMIM: "Hyperparathyroidism" [OMIM:Hyperparathyroidism]
UMLS:C0020502 "Hyperparathyroidism" [HPO:0000843]
Is a (Direct Parents):
Orphanet Abnormality of the parathyroid gland
HPO         Abnormality of the parathyroid physiology
MedDRA Hyperparathyroid disorders
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)
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)