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Sneddon syndrome

Disease Summary
Associated Targets (1)
Tbio

1


Explore Associated Targets
Mondo Description Sneddon's syndrome (SS) is a rare non-inflammatory thrombotic vasculopathy characterized by the combination of cerebrovascular disease with livedo racemosa.
Uniprot Description A systemic non-inflammatory thrombotic vasculopathy characterized by the association of livedo racemosa, and in some cases livedo reticularis, with cerebrovascular disease. Livedo racemosa is a persistent net-like violaceous-cyanotic, mottled discoloration of the skin affecting the legs, the arms, the buttocks and the trunk; livedo reticularis is limited to the extremities and is visible only in the cold. Cerebrovascular features include recurrent transient ischemic attacks, infarcts, and rarely spinal strokes or intracranial or subarachnoid hemorrhages. Headache and vertigo may precede the onset of livedo racemosa and cerebrovascular manifestations by several years. Rare neurologic symptoms include seizures, chorea, or myelopathies.
Mondo Term and Equivalent IDs
MONDO:0008436:  Sneddon syndrome
EFO:1001186: 
GARD:0007664: 
MESH:D018860: 
Orphanet:820: 
SCTID:238776001: 
UMLS:C0282492: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Parents
Tbio

5032

Tdark

1219

Tchem

988

Tclin

348

Tbio

2492

Tchem

471

Tdark

416

Tclin

158

Tbio

966

Tchem

292

Tclin

207

Tdark

108

Tbio

638

Tchem

112

Tdark

111

Tclin

100

Tbio

119

Tchem

37

Tclin

19

Tdark

8

Children
Target Novelty (Tin-x)