Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Colloid cyst of pituitary gland (disorder) |
Finding site |
False |
Pituitary structure |
Inferred relationship |
Some |
1 |
Invasive pituitary adenoma |
Finding site |
False |
Pituitary structure |
Inferred relationship |
Some |
1 |
Colloid cyst of pituitary gland (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Functionless pituitary neoplasm (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Invasive pituitary adenoma |
Finding site |
False |
Pituitary structure |
Inferred relationship |
Some |
1 |
Functioning pituitary neoplasm (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Pituicytoma |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Familial isolated pituitary adenoma |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Ectopic pituitary tissue |
Finding site |
False |
Pituitary structure |
Inferred relationship |
Some |
2 |
Congenital absence of pituitary gland |
Finding site |
False |
Pituitary structure |
Inferred relationship |
Some |
2 |
Accessory pituitary gland |
Finding site |
False |
Pituitary structure |
Inferred relationship |
Some |
2 |
Congenital anomaly of pituitary gland |
Finding site |
False |
Pituitary structure |
Inferred relationship |
Some |
2 |
Pharyngeal pituitary tissue |
Finding site |
False |
Pituitary structure |
Inferred relationship |
Some |
4 |
Ectopic pituitary tissue |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
A rare pituitary deficiency characterized by herniation of the subarachnoid space into the sella turcica, resulting in flattening of the pituitary gland and endocrine dysfunction. Most common endocrine abnormalities are hyperprolactinemia and growth hormone deficit. Clinical symptoms are highly variable and include headaches, irregular menstruation, galactorrhea, obesity, and visual disturbances, among others. |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
2 |
Choroideremia co-occurrent with hypopituitarism |
Finding site |
False |
Pituitary structure |
Inferred relationship |
Some |
|
Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies. Congenital hypopituitarism is rare compared with the high incidence of hypopituitarism induced by pituitary adenomas, transsphenoidal surgery or radiotherapy. |
Finding site |
False |
Pituitary structure |
Inferred relationship |
Some |
|
Hypopituitarism following procedure (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
2 |
Familial isolated pituitary adenoma |
Finding site |
False |
Pituitary structure |
Inferred relationship |
Some |
2 |
Choroideremia co-occurrent with hypopituitarism |
Finding site |
False |
Pituitary structure |
Inferred relationship |
Some |
1 |
Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies. Congenital hypopituitarism is rare compared with the high incidence of hypopituitarism induced by pituitary adenomas, transsphenoidal surgery or radiotherapy. |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
A rare genetic, syndromic retinal disorder characterized by the association of retinitis pigmentosa, hypopituitarism, nephronophthisis, and skeletal dysplasia. |
Finding site |
False |
Pituitary structure |
Inferred relationship |
Some |
6 |
Hypopituitarism due to radiotherapy |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Pharyngeal pituitary tissue |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
2 |
A rare genetic, syndromic retinal disorder characterized by the association of retinitis pigmentosa, hypopituitarism, nephronophthisis, and skeletal dysplasia. |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
2 |
A rare midline cerebral malformation characterized by duplicated pituitary stalks and/or glands within duplicated sella. Patients may present various degrees of facial dysmorphism and endocrine abnormalities, including precocious puberty, hypogonadism, hypothyroidism and/or hyperprolactinemia, as well as associated congenital anomalies, such as clift lip/palate, bifid nasal bridge/tongue/uvula, hypothalamic enlargement with or without hamartoma, nasopharyngeal tumors, corpus callosum agenesis/hypoplasia, basilar artery duplication, and/or vertebral defects (in particular, duplication of the odontoid process). |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
A rare, mixed, functioning pituitary adenoma characterized by the cosecretion of growth hormone and prolactin, which manifests with signs and symptoms of both acromegaly and hyperprolactinemia. |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Pituitary dermoid and epidermoid cysts is a rare, acquired pituitary hormone deficiency characterised by the presence of rare, benign tumour in the sellar region. Clinical presentation is either acute or insidious, and is variable according to the cyst location, size and potential rupture. Most commonly patients present with headache, visual disturbances, and pituitary dysfunction. |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Pituitary dermoid and epidermoid cysts is a rare, acquired pituitary hormone deficiency characterised by the presence of rare, benign tumour in the sellar region. Clinical presentation is either acute or insidious, and is variable according to the cyst location, size and potential rupture. Most commonly patients present with headache, visual disturbances, and pituitary dysfunction. |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
2 |
A rare, acquired pituitary hormone deficiency characterized by combination of headache, visual field defects that correlate with cyst size, and pituitary dysfunction. Most frequent hormonal manifestations are hypogonadism with amenorrhea/impotence or low libido and galactorrhea. |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Septo-optic dysplasia sequence |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Malignant pituitary blastoma (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Hypopituitarism caused by drug (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Epidermoid cyst of pituitary gland (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Transsphenoidal partial excision of neoplasm of pituitary gland (procedure) |
Procedure site - Direct (attribute) |
False |
Pituitary structure |
Inferred relationship |
Some |
1 |
Transsphenoidal total excision of neoplasm of pituitary gland (procedure) |
Procedure site - Direct (attribute) |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Endoscopic endonasal transsphenoidal total excision of neoplasm of pituitary gland |
Procedure site - Direct (attribute) |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Endoscopic endonasal transsphenoidal partial excision of neoplasm of pituitary gland |
Procedure site - Direct (attribute) |
False |
Pituitary structure |
Inferred relationship |
Some |
1 |
A benign tumor invasive into adjacent structures. |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Adenocarcinoma of pituitary gland |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Xanthogranulomatous hypophysitis (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Autoimmune hypopituitarism (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Hypopituitarism due to granulomatous disease |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Hypopituitarism due to metabolic disease (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Hypopituitarism due to vascular disorder |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Immunoglobulin G4 related hypophysitis (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Incision and exploration of pituitary gland |
Procedure site - Direct (attribute) |
True |
Pituitary structure |
Inferred relationship |
Some |
2 |
Microprolactinoma |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
2 |
Macroprolactinoma |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
2 |
Prolactinoma |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
2 |
Pituitary hypertrophy |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Pituitary degeneration |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Avascular necrosis of pituitary gland (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Isolated deficiency of pituitary hormone (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Metastatic carcinoma to pituitary (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Metastatic adenocarcinoma to pituitary gland (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Primary adenocarcinoma of pituitary gland (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor. |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Structure of transplanted pituitary gland (body structure) |
Is a |
True |
Pituitary structure |
Inferred relationship |
Some |
|
Excision of neoplasm of pituitary (procedure) |
Procedure site - Direct (attribute) |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Magnetic resonance imaging of pituitary gland (procedure) |
Procedure site - Direct (attribute) |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Malignant neoplasm of pituitary and hypothalamus |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
2 |
A rare, acquired pituitary hormone deficiency characterised by inflammation of the pituitary gland secondary to immunotherapy for cancer treatments (such as monoclonal antibodies against cytotoxic T lymphocytes antigen, programmed cell death protein-1, and programmed cell death ligand molecules). Major clinical features include headache, fatigue, adrenal insufficiency and hypothyroidism. Patients may also have nausea and vomiting associated to the headache as well as dizziness and hot flashes. Enlargement of the pituitary gland is present in the brain imaging. |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |
Inflammation of pituitary caused by drug (disorder) |
Finding site |
True |
Pituitary structure |
Inferred relationship |
Some |
1 |