Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Exploration of parathyroid transplant |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Isotope stat scan parathyroid (procedure) |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Excision of parathyroid transplant |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Anomaly of parathyroid gland NEC NOS |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Parathyroid carcinoma (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Other specified excision of parathyroid gland |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Carcinoma in situ of parathyroid gland |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Other specified other operation on parathyroid gland |
Procedure site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Other operation on parathyroid gland NOS |
Procedure site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Other operations on parathyroid gland |
Procedure site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Reexploration of parathyroid gland |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital absence of parathyroid gland |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Parathyroid hyperplasia |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
MRI of parathyroid |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Contusion of parathyroid gland |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Excision of lesion of parathyroid glands (procedure) |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Parathyroid tissue sample |
Specimen source topography |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Excised parathyroid specimen (specimen) |
Specimen source topography |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
CT of parathyroid |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autoimmune parathyroiditis |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Radionuclide parathyroid subtraction study |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Endoscopy of parathyroid gland |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Parathyroid biopsy specimen |
Specimen source topography |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Imaging of parathyroid using technetium 99m thallium 201 |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Single photon emission computed tomography of parathyroid using technetium 99m thallium 201 |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Specimen from parathyroid obtained by fine needle aspiration biopsy (specimen) |
Specimen source topography |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Single photon emission computed tomography of parathyroid (procedure) |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Radionuclide imaging of parathyroid using metaiodobenzylguanidine (procedure) |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Imaging of parathyroid iusing iodine 123 meta-iodobenzylguanidine |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Exploration of parathyroid with mediastinal exploration by sternal split approach |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Parathyroid gland hematoma |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Fine needle aspiration biopsy of parathyroid gland (procedure) |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Single photon emission computed tomography of parathyroid using technetium 99m thallium 201 |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Biopsy of parathyroid gland |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Single photon emission computed tomography of parathyroid (procedure) |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Radionuclide imaging of parathyroid using metaiodobenzylguanidine (procedure) |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Specimen from parathyroid obtained by fine needle aspiration biopsy (specimen) |
Specimen source topography |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Imaging of parathyroid using technetium 99m thallium 201 |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Imaging of parathyroid iusing iodine 123 meta-iodobenzylguanidine |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Manipulation of parathyroid gland |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Single photon emission computed tomography using technetium 99m thallium 201 with computed tomography of parathyroid |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Single photon emission computed tomography with computed tomography of parathyroid (procedure) |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Single photon emission computed tomography of parathyroid (procedure) |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Single photon emission computed tomography using technetium 99m thallium 201 with computed tomography of parathyroid |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Single photon emission computed tomography with computed tomography of parathyroid (procedure) |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Radionuclide imaging of parathyroid using metaiodobenzylguanidine (procedure) |
Procedure site - Direct (attribute) |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
22q11 microdeletion with complete DiGeorge sequence |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Hyperparathyroidism-jaw tumor syndrome (disorder) |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital anomaly of parathyroid glands (disorder) |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Congenital absence of parathyroid gland |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Aberrant parathyroid gland |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Aplasia of parathyroid gland (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ectopic hyperparathyroidism |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Parathyromatosis |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Ectopic parathyroid hormone-related protein secretion |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Secondary hyperparathyroidism of nonrenal origin (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hypomagnesemia with secondary hypocalcemia (disorder) |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal severe primary hyperparathyroidism (NSHPT) is characterised by severe hypercalcaemia (> 3.5 mM) from birth and associated with major hyperparathyroidism. |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Hyperparathyroidism due to end stage renal disease on dialysis (disorder) |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Hypoparathyroidism due to impaired PTH secretion |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland (disorder) |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypoparathyroidism after iodine thyroid ablation (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Hypoparathyroidism after external beam radiotherapy (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Hypoparathyroidism due to hemochromatosis (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Transient neonatal hypoparathyroidism due to maternal hyperparathyroidism (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Secondary hypoparathyroidism (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hypoparathyroidism due to granulomatous disease (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
A rare multiple congenital anomalies/dysmorphic syndrome characterized by the association of congenital hypoparathyroidism, nephropathy, congenital lymphedema, mitral valve prolapse and brachytelephalangy. Additional features include mild facial dysmorphism, hypertrichosis, and nail abnormalities. There have been no further descriptions in the literature since 1993. |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypoparathyroidism following procedure (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Nephropathy, deafness, hyperparathyroidism syndrome |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Hypoparathyroidism, deafness, renal disease syndrome (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
10 |
Iodine 123 technetium 99m methoxyisobutylisonitrile radionuclide parathyroid subtraction study (procedure) |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Iodine 123 technetium 99m methoxyisobutylisonitrile radionuclide parathyroid subtraction study (procedure) |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Hyperparathyroidism-jaw tumor syndrome (disorder) |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hypomagnesemia with secondary hypocalcemia (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare multiple congenital anomalies/dysmorphic syndrome characterized by the association of congenital hypoparathyroidism, nephropathy, congenital lymphedema, mitral valve prolapse and brachytelephalangy. Additional features include mild facial dysmorphism, hypertrichosis, and nail abnormalities. There have been no further descriptions in the literature since 1993. |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism causing hypocalcemia due to insufficient serum levels of bioactive parathormone (PTH), without other endocrine disorders or developmental defects. |
Finding site |
False |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Dual isotope single photon emission computed tomography of parathyroid using technetium-99m and thallium-201 (procedure) |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Dual isotope single photon emission computed tomography of parathyroid using technetium-99m and thallium-201 (procedure) |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dual isotope single photon emission computed tomography with computed tomography of parathyroid using technetium-99m and thallium-201 (procedure) |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Dual isotope single photon emission computed tomography with computed tomography of parathyroid using technetium-99m and thallium-201 (procedure) |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Dual isotope single photon emission computed tomography with computed tomography of parathyroid using technetium-99m and thallium-201 (procedure) |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hyperparathyroidism due to end stage renal disease on dialysis (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Radionuclide imaging of parathyroid using technetium (99m-Tc) and thallium-201 |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Radionuclide imaging of parathyroid using technetium (99m-Tc) and thallium-201 |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Operation on parathyroid gland during thyroidectomy |
Procedure site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A rare multiple congenital anomalies/dysmorphic syndrome characterized by the association of congenital hypoparathyroidism, nephropathy, congenital lymphedema, mitral valve prolapse and brachytelephalangy. Additional features include mild facial dysmorphism, hypertrichosis, and nail abnormalities. There have been no further descriptions in the literature since 1993. |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Parathyroid adenoma excision |
Procedure site - Indirect (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Exploration of parathyroid with mediastinal exploration by transthoracic approach |
Procedure site - Direct (attribute) |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare hereditary familial primary hyperparathyroidism disease with characteristics of primary hyperparathyroidism due to single or multiple parathyroid tumours in at least two first-degree relatives in the absence of evidence of other endocrine disorders, tumours and/or systemic manifestations. |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pseudopseudohypoparathyroidism (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pseudohypoparathyroidism type II (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pseudohypoparathyroidism type I B |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pseudohypoparathyroidism type I A |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Pseudohypoparathyroidism |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pseudohypoparathyroidism type 1C (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism causing hypocalcemia due to insufficient serum levels of bioactive parathormone (PTH), without other endocrine disorders or developmental defects. |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hyperparathyroidism-jaw tumor syndrome (disorder) |
Finding site |
True |
Parathyroid structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |