Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire multiple endocrine glands |
Is a |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
|
Overlapping malignant neoplasm of multiple endocrine glands |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
|
Polyglandular hyperfunction |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Combination of endocrine dysfunction |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Multiple endocrine deficiency syndrome |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Polyglandular dysfunction |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
A rare genetic disease that manifests in childhood or early adolescence with a combination of chronic mucocutaneous candidiasis, hypoparathyroidism and autoimmune adrenal failure. The first manifestation of the disease (usually candidiasis) occurs in childhood with other manifestations appearing progressively. The most common autoimmune endocrine involvement is hypoparathyroidism (79-96% of cases). Adrenal failure most often manifests with concurrent mineralocorticoid and glucocorticoid deficiency (78% of cases). The disease is caused by mutations of the AIRE gene (21q22.3) coding for the AIRE transcription factor, which is involved in immune tolerance mechanisms and contributes to the negative selection of autoreactive T lymphocytes in the thymus, lymph nodes and spleen. Transmission is autosomal recessive. |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
|
Neoplasm of multiple endocrine glands |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Polyglandular dysfunction AND/OR related disorders |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Multiple endocrine neoplasia, type 1 |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Autoimmune polyendocrinopathy |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
|
Polyglandular activity in multiple endocrine adenomatosis |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Multiple endocrine neoplasia, type 2b |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Multiple endocrine neoplasia, type 2 |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Carpenters syndrome |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
|
Polyglandular autoimmune syndrome, type 2 |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
|
Benign neoplasm of multiple endocrine glands |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Carcinoma in situ of multiple endocrine glands |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Primary malignant neoplasm of multiple endocrine glands |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Metastatic malignant neoplasm to multiple endocrine glands |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Neoplasm of uncertain behavior of multiple endocrine glands |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Other specified polyglandular dysfunction |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
|
Polyglandular dysfunction NOS |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
|
[X]Other polyglandular dysfunction |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
|
Other combinations of endocrine dysfunction |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
|
benignt neoplasme med involvering af flere hormonproducerende kirtler |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Carcinoma in situ of multiple endocrine glands |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Neoplasm of uncertain behavior of multiple endocrine glands |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Multiple endocrine neoplasia, type 2 |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Neoplasm of multiple endocrine glands |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Multiple endocrine neoplasia, type 1 |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
benignt neoplasme med involvering af flere hormonproducerende kirtler |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Metastatic malignant neoplasm to multiple endocrine glands |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Benign neoplasm of multiple endocrine glands |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Polyglandular activity in multiple endocrine adenomatosis |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Multiple endocrine neoplasia, type 2b |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Primary malignant neoplasm of multiple endocrine glands |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Autoimmune polyendocrine syndrome type 4 |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
|
Autoimmune polyendocrine syndrome type 3 (disorder) |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
|
Multiple endocrine neoplasia, type 1 |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
2 |
Benign multiple endocrine neoplasia type 2a |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Malignant multiple endocrine neoplasia type 2a (disorder) |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Multiple endocrine neoplasia type 4 (MEN4) is a very rare form of MEN, an inherited cancer syndrome, characterized by parathyroid and anterior pituitary tumors, possibly associated with adrenal, renal, and reproductive organ tumors. |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Multiple endocrine neoplasia type 2A (disorder) |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Carney-Stratakis syndrome is a recently described familial syndrome characterized by gastrointestinal stromal tumors (GIST) and paragangliomas, often at multiple sites. |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
3 |
A rare endocrine disease characterized by lentigines with a specific peri-orifical distribution, blue nevus, myxomas, various endocrine tumors including primary pigmented nodular adrenocortical disease (PPNAD), acromegaly, thyroid tumors, and a wide range of other tumors. |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
4 |
A rare non-hereditary condition characterised by gastrointestinal stromal tumours (GIST, intramural mesenchymal tumours of the gastrointestinal tract with neuronal or neural crest cell origin), pulmonary chondromas and extraadrenal paragangliomas. |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
A rare endocrine disease characterized by lentigines with a specific peri-orifical distribution, blue nevus, myxomas, various endocrine tumors including primary pigmented nodular adrenocortical disease (PPNAD), acromegaly, thyroid tumors, and a wide range of other tumors. |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
3 |
Multiple endocrine neoplasia, type 2 |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
2 |
Multiple endocrine neoplasia type 2A (disorder) |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
2 |
Benign multiple endocrine neoplasia type 2a |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
2 |
Malignant multiple endocrine neoplasia type 2a (disorder) |
Finding site |
False |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
2 |
Autoimmune polyendocrinopathy |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Polyglandular autoimmune syndrome, type 2 |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Autoimmune polyendocrine syndrome type 4 |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Autoimmune polyendocrine syndrome type 3 (disorder) |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
A rare genetic disease that manifests in childhood or early adolescence with a combination of chronic mucocutaneous candidiasis, hypoparathyroidism and autoimmune adrenal failure. The first manifestation of the disease (usually candidiasis) occurs in childhood with other manifestations appearing progressively. The most common autoimmune endocrine involvement is hypoparathyroidism (79-96% of cases). Adrenal failure most often manifests with concurrent mineralocorticoid and glucocorticoid deficiency (78% of cases). The disease is caused by mutations of the AIRE gene (21q22.3) coding for the AIRE transcription factor, which is involved in immune tolerance mechanisms and contributes to the negative selection of autoreactive T lymphocytes in the thymus, lymph nodes and spleen. Transmission is autosomal recessive. |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
3 |
Atrophy of multiple endocrine glands (disorder) |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Dystrophy of multiple endocrine glands (disorder) |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Sclerosis of multiple endocrine glands (disorder) |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Deficiency of multiple endocrine glands (disorder) |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
1 |
Carney complex-associated-primary pigmented nodular adrenocortical disease (disorder) |
Finding site |
True |
Structure of multiple endocrine glands |
Inferred relationship |
Some |
3 |