Skin vascular disease
MONDO:0019293A disease that involves the superficial vasculature.
Also known as: skin vascular disorder, superficial vasculature disease, vascular disease of the skin, vascular skin disease, vasculature skin disease, disorder of blood vessels affecting skin, vascular disorder of skin, vascular disorders of skin
134 clinical trials for this condition and its sub-types, 5 tagged with Skin vascular disease itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Skin vascular disease
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Angioedema 19 trials · 66 incl. sub-types
3 sub-types
- Hereditary angioedema 58 trials · 60 incl. sub-types Sub-types →
- Acquired angioedema 2 trials · 3 incl. sub-types Sub-types →
- Non-histaminic angioedema 2 trials
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Behcet disease 37 trials
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Familial multiple nevi flammei 12 trials
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Livedo reticularis 3 trials
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Chilblain lupus 1 trial · 3 incl. sub-types
1 sub-type
- Familial chilblain lupus 2 trials Sub-types →
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Maffucci syndrome 2 trials
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Sneddon syndrome 2 trials
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Blue rubber bleb nevus 2 trials
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Malignant atrophic papulosis 2 trials
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Pityriasis lichenoides 1 trial
1 sub-type
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Bockenheimer syndrome 0 trials
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Cobb syndrome 0 trials
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Wyburn-Mason syndrome 0 trials
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Angioma serpiginosum 0 trials
2 sub-types
- Angioma serpiginosum, X-linked 0 trials
- Angioma serpiginosum, autosomal dominant 0 trials
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Atrophic papulosis 0 trials
1 sub-type
- Benign atrophic papulosis 0 trials
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Calciphylaxis cutis 0 trials
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Cutaneous collagenous vasculopathy 0 trials
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Generalized essential telangiectasia 0 trials
Most studied deeper sub-types
Hereditary angioedema type 1
(26)
Hereditary angioedema type 2
(26)
Hereditary angioedema with C1Inh deficiency
(14)
Hereditary angioedema type 3
(2)
Hereditary angioedema with normal C1Inh
(2)
Renin-angiotensin-aldosterone system-blocker-induced angioedema
(2)
Acquired angioedema with C1Inh deficiency
(1)
Acquired angioedema type 1
(0)
Acquired angioedema type 2
(0)
Angioedema, hereditary, 4
(0)
Angioedema, hereditary, 5
(0)
Angioedema, hereditary, 6
(0)
Angioedema, hereditary, 7
(0)
Angioedema, hereditary, 8
(0)
Chilblain lupus 1
(0)
Chilblain lupus 2
(0)
Febrile ulceronecrotic Mucha-Habermann disease
(0)
Hereditary angioedema with normal C1inh not related to F12 or PLG variant
(0)
PLG-related hereditary angioedema with normal C1inh
(0)
Vibratory angioedema
(0)