Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Structure of lymphatic vessel of small intestine (body structure) |
Is a |
True |
Structure of lymphatic vessel of intestine (body structure) |
Inferred relationship |
Some |
|
struktur af lymfekar i appendix og tyktarmen |
Is a |
False |
Structure of lymphatic vessel of intestine (body structure) |
Inferred relationship |
Some |
|
Intestinal lymphangiectasis |
Finding site |
False |
Structure of lymphatic vessel of intestine (body structure) |
Inferred relationship |
Some |
1 |
Primary lymphangiectasis of intestine (disorder) |
Finding site |
True |
Structure of lymphatic vessel of intestine (body structure) |
Inferred relationship |
Some |
2 |
Intestinal lymphangiectasis |
Finding site |
True |
Structure of lymphatic vessel of intestine (body structure) |
Inferred relationship |
Some |
1 |
Secondary intestinal lymphangiectasia |
Finding site |
False |
Structure of lymphatic vessel of intestine (body structure) |
Inferred relationship |
Some |
1 |
Secondary intestinal lymphangiectasia is an acquired from of intestinal lymphangiectasia manifesting as a protein-losing enteropathy due to another disorder such as Crohn's disease, congestive heart failure, sarcoidosis, Turner syndrome and often in patients who have undergone a Fontan operation. It is characterised by malabsorption, diarrhoea, oedema due hypoproteinaemia, steatorrhoea and serosal effusions. |
Finding site |
True |
Structure of lymphatic vessel of intestine (body structure) |
Inferred relationship |
Some |
1 |
An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to intestinal lymphangiectasia. There have been no further descriptions in the literature since 1985. |
Finding site |
False |
Structure of lymphatic vessel of intestine (body structure) |
Inferred relationship |
Some |
3 |
Entire lymphatic vessel of intestine (body structure) |
Is a |
True |
Structure of lymphatic vessel of intestine (body structure) |
Inferred relationship |
Some |
|
An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to intestinal lymphangiectasia. There have been no further descriptions in the literature since 1985. |
Finding site |
True |
Structure of lymphatic vessel of intestine (body structure) |
Inferred relationship |
Some |
1 |
Hennekam lymphangiectasia-lymphedema syndrome (disorder) |
Finding site |
True |
Structure of lymphatic vessel of intestine (body structure) |
Inferred relationship |
Some |
2 |
Structure of lymphatic vessel of large intestine |
Is a |
True |
Structure of lymphatic vessel of intestine (body structure) |
Inferred relationship |
Some |
|