Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Reconstruction of trunk using myocutaneous flap (procedure) |
Procedure site - Direct (attribute) |
True |
Trunk structure (body structure) |
Inferred relationship |
Some |
1 |
Reconstruction of trunk using muscle flap (procedure) |
Procedure site - Direct (attribute) |
True |
Trunk structure (body structure) |
Inferred relationship |
Some |
1 |
A rare familial partial lipodystrophy characterized by adult onset of distal lipoatrophy with gluteofemoral fat loss, as well as increased fat accumulation in the face and trunk and visceral adiposity. Additional manifestations include diabetes mellitus, atherogenic dyslipidemia, eyelid xanthelasmas, arterial hypertension, cardiovascular disease, hepatic steatosis, acanthosis nigricans on axillae and neck, hirsutism, and muscular hypertrophy of the lower limbs. |
Finding site |
True |
Trunk structure (body structure) |
Inferred relationship |
Some |
2 |
A rare familial partial lipodystrophy characterized by adult onset of distal lipoatrophy and severe insulin resistance in the liver and peripheral tissues, hyperinsulinemia, and diabetes mellitus. Acanthosis nigricans and hypertension have been reported in association. |
Finding site |
True |
Trunk structure (body structure) |
Inferred relationship |
Some |
2 |
A rare familial partial lipodystrophy characterized by severe partial lipoatrophy affecting the limbs, trunk, and abdomen, together with faciocervical fat accumulation. Additional manifestations include diabetes, acanthosis nigricans, liver steatosis, and hypertriglyceridemia, as well as low serum leptin and adiponectin levels. Severe cardiac rhythm and conduction disturbances have also been reported. |
Finding site |
True |
Trunk structure (body structure) |
Inferred relationship |
Some |
2 |
A rare, genetic lipodystrophy characterized by abnormal subcutaneous fat distribution, resulting in preservation of visceral, neck and axillary fat and absence of lower limb and femoro gluteal subcutaneous fat. Additional clinical features are acanthosis nigricans, insulin-resistant type II diabetes mellitus, dyslipidemia, and hypertension, leading to pancreatitis, hepatomegaly and hepatic steatosis. |
Finding site |
True |
Trunk structure (body structure) |
Inferred relationship |
Some |
3 |
A rare, genetic lipodystrophy characterized by abnormal subcutaneous fat distribution, resulting in excess accumulation of fat in the face, neck, shoulders, axillae, trunk and pubic region, and loss of subcutaneous fat from the lower extremities. Variable common additional features are progressive adult onset myopathy, insulin resistance, diabetes, hypertriglyceridemia, hepatic steatosis, and vitiligo. |
Finding site |
True |
Trunk structure (body structure) |
Inferred relationship |
Some |
3 |
Harvest of flap of skin and muscle of trunk |
Procedure site - Direct (attribute) |
False |
Trunk structure (body structure) |
Inferred relationship |
Some |
1 |
Bite wound of trunk (disorder) |
Finding site |
True |
Trunk structure (body structure) |
Inferred relationship |
Some |
1 |
Primary rhabdomyosarcoma of trunk (disorder) |
Finding site |
True |
Trunk structure (body structure) |
Inferred relationship |
Some |
1 |
Lethal congenital disproportionate short trunk short stature |
Finding site |
True |
Trunk structure (body structure) |
Inferred relationship |
Some |
1 |
Splinter in trunk with infection |
Finding site |
True |
Trunk structure (body structure) |
Inferred relationship |
Some |
1 |