Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire capillary of skin |
Is a |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
|
Cobb's syndrome |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
4 |
Bregeat's syndrome |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
2 |
Sturge-Weber syndrome |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
4 |
Roberts-SC phocomelia syndrome |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Port-wine stain of skin |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Port-wine stain of skin (disorder) |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Port-wine stain of skin (disorder) |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Bregeat's syndrome |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
2 |
Port-wine stain of skin (disorder) |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Port-wine stain of skin (disorder) |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
2 |
Cutaneous capillary malformation (disorder) |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Capillary malformation-arteriovenous malformation syndrome |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
3 |
A rare congenital complex vascular malformation syndrome characterized by capillary malformations manifesting as wine stains and venous varicosities typically prominent along the lateral aspect of the lower extremities, associated with overgrowth of a limb (most commonly a leg, less frequently other regions of the body), involving bone and/or soft tissues. The diagnosis is usually made in presence of at least two of these three features. Lymphatic malformations are also observed, while arteriovenous fistulas are absent. Patients present recurrent painful thrombophlebitis, venous thrombosis, and sudden venous hemorrhage. |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
3 |
syndrome d'autisme-angiome facial |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Familial multiple nevi flammei is a rare, genetic capillary malformation disorder characterized by dark red to purple birthmarks which manifest as flat, sharply circumscribed cutaneous lesions, typically situated in the head and neck region, in various members of a single family. The lesions grow proportionally with the individual, change in color and often thicken with age. |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Capillary malformation-arteriovenous malformation syndrome |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
A rare congenital complex vascular malformation syndrome characterized by capillary malformations manifesting as wine stains and venous varicosities typically prominent along the lateral aspect of the lower extremities, associated with overgrowth of a limb (most commonly a leg, less frequently other regions of the body), involving bone and/or soft tissues. The diagnosis is usually made in presence of at least two of these three features. Lymphatic malformations are also observed, while arteriovenous fistulas are absent. Patients present recurrent painful thrombophlebitis, venous thrombosis, and sudden venous hemorrhage. |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
A rare developmental defect during embryogenesis syndrome characterized by a glabellar capillary malformation, congenital communicating hydrocephalus, and posterior fossa brain abnormalities, including Dandy-Walker malformation, cerebellar vermis agenesis, and mega cisterna magna. Seizures are occasionally associated. There have been no further descriptions in the literature since 1979. |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
3 |
Salmon patch naevus |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Multiple angiomatous naevi of skin |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Multiple progressive haemangiomata |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
2 |
Ulcero - mutilating haemangiomatosis |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
2 |
Vascular birthmark |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Nevus anemicus |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Port-wine stain associated with spinal dysraphism (disorder) |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Angiomatous nevus with complication |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Ulcerated angiomatous nevus (disorder) |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
2 |
Angiomatous nevus impairing vision (disorder) |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Angioma serpiginosum |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Strawberry nevus of skin |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Hemangioma of skin in pregnancy (disorder) |
Finding site |
False |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Port-wine stain in proteus syndrome (disorder) |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Abnormal vision due to superficial infantile haemangioma of periorbital region |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
2 |
Superficial infantile hemangioma of periorbital region |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
2 |
Videocapillaroscopy of nailfold |
Procedure site - Direct (attribute) |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
Progressive pigmentary dermatosis of Schamberg |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
2 |
Pigmented purpuric dermatosis (disorder) |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
2 |
Purpura pigmentosa chronica |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
5 |
Purpura annularis telangiectodes of Majocchi |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
2 |
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
3 |
Eczematid-like purpura of Doucas and Kapetanakis |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
2 |
Lichen aureus |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
3 |
Familial pigmented purpuric eruption |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |
A rare disease with characteristics of capillary malformation and soft tissue hypertrophy. The cause is unknown however GNA11 mutation has been reported in some patients. Capillary malformation in this disease has characteristics of widespread reticulated erythematous patches. The associated overgrowth is proportionate and is not progressive. |
Finding site |
True |
Structure of capillary of skin |
Inferred relationship |
Some |
1 |