Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Histiocytosis X syndrome |
Is a |
False |
Histiocytic syndrome |
Inferred relationship |
Some |
|
anémie hémolytique auto-immune avec érythrophagocytose (Fc portion de l'auto-anticorps) |
Is a |
False |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Langerhan's cell histiocytosis |
Is a |
False |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Benign cephalic histiocytosis |
Is a |
True |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Hemophagocytic syndrome |
Is a |
False |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Malignant histiocytic disorder |
Is a |
False |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Rosai-Dorfman disease |
Is a |
False |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Sea-blue histiocyte syndrome |
Is a |
True |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Langerhans cell histiocytosis |
Is a |
False |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Xanthogranuloma |
Is a |
True |
Histiocytic syndrome |
Inferred relationship |
Some |
|
[X]Other histiocytosis syndromes |
Is a |
False |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Histiocytic and mast cell tumor of uncertain behavior |
Is a |
False |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Neoplasm of uncertain behavior of histiocytic and mast cells |
Is a |
False |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Xanthoma disseminatum (disorder) |
Is a |
True |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Juvenile xanthogranuloma (disorder) |
Is a |
False |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Multiple eruptive juvenile xanthogranuloma (disorder) |
Is a |
False |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Non-Langerhans cell histiocytic dermatosis (disorder) |
Is a |
True |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Mucinous histiocytosis of the colon |
Is a |
True |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Lipoid dermatoarthritis |
Is a |
False |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Cytophagic histiocytic panniculitis (disorder) |
Associated with |
True |
Histiocytic syndrome |
Inferred relationship |
Some |
2 |
Panniculitis secondary to histiocytic disorder (disorder) |
Associated with |
True |
Histiocytic syndrome |
Inferred relationship |
Some |
2 |
Erdheim-Chester disease |
Is a |
False |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Chronic histiocytosis |
Is a |
True |
Histiocytic syndrome |
Inferred relationship |
Some |
|
History of histiocytosis (situation) |
Associated finding |
True |
Histiocytic syndrome |
Inferred relationship |
Some |
1 |
Periodontitis due to histiocytosis syndrome (disorder) |
Due to |
True |
Histiocytic syndrome |
Inferred relationship |
Some |
1 |
A rare cutaneous disease and a systemic inherited histiocytosis mainly characterised by hyperpigmentation, hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, low height, and occasionally, hyperglycaemia/diabetes mellitus. Due to overlapping clinical features, it is now considered to include pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome (PHID), Faisalabad histiocytosis (FHC) and familial sinus histiocytosis with massive lymphadenopathy (FSHML). Some cases of dysosteosclerosis may also represent the syndrome. |
Is a |
True |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Histiocytic neoplasm (disorder) |
Is a |
True |
Histiocytic syndrome |
Inferred relationship |
Some |
|
Haemophagocytic lymphohistiocytosis |
Is a |
True |
Histiocytic syndrome |
Inferred relationship |
Some |
|