Elevated circulating parathyroid hormone level

Symptom Information:

Symptom ID: HPO:0003165
Synonyms:
Elevated serum parathyroid hormone [HPO:0003165]
Elevated serum parathyroid hormone level [HPO:0003165]
Elevated serum pth [HPO:0003165]
Increased serum parathyroid hormone [HPO:0003165]
Elevated serum PTH [OMIM:Elevated serum PTH]
Elevated serum parathyroid hormone [OMIM:Elevated serum parathyroid hormone]
Increased serum parathyroid hormone [OMIM:Increased serum parathyroid hormone]
Elevated serum parathyroid hormone (PTH) [OMIM:Elevated serum parathyroid hormone (PTH)]
Elevated serum parathyroid hormone (PTH) level [OMIM:Elevated serum parathyroid hormone (PTH) level]
Increased serum parathyroid hormone (PTH) [OMIM:Increased serum parathyroid hormone (PTH)]
Quality:
Cross references:
OMIM: "Elevated serum PTH" [OMIM:Elevated serum PTH]
OMIM: "Elevated serum parathyroid hormone" [OMIM:Elevated serum parathyroid hormone]
OMIM: "Increased serum parathyroid hormone" [OMIM:Increased serum parathyroid hormone]
OMIM: "Elevated serum parathyroid hormone (PTH)" [OMIM:Elevated serum parathyroid hormone (PTH)]
OMIM: "Elevated serum parathyroid hormone (PTH) level" [OMIM:Elevated serum parathyroid hormone (PTH) level]
OMIM: "Increased serum parathyroid hormone (PTH)" [OMIM:Increased serum parathyroid hormone (PTH)]
Is a (Direct Parents):
HPO         Abnormality of calcium-phosphate metabolism
HPO         Abnormality of circulating hormone level
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Abnormality of circulating hormone level(HPO:0003117)
             Elevated circulating parathyroid hormone level(HPO:0003165)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of calcium-phosphate metabolism(HPO:0100530)
             Elevated circulating parathyroid hormone level(HPO:0003165)
MedDRA:
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:101800)
Acrodysostosis with multiple hormone resistance (Orphanet:280651)
Albright hereditary osteodystrophy (Orphanet:665)
CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (OMIM:122860)
Craniodiaphyseal dysplasia (Orphanet:1513)
HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM (OMIM:612089)
Hypocalcemic vitamin D-dependent rickets (Orphanet:289157)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Neonatal severe primary hyperparathyroidism (Orphanet:417)
Pseudohypoparathyroidism type 1A (Orphanet:79443)
Pseudohypoparathyroidism type 1B (Orphanet:94089)
Pseudohypoparathyroidism type 1C (Orphanet:79444)
Pseudohypoparathyroidism type 2 (Orphanet:94090)
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A (OMIM:264700)
VITAMIN D-DEPENDENT RICKETS, TYPE 2A (OMIM:277440)
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR (OMIM:600785)
X-linked hypophosphatemia (Orphanet:89936)