Sneddon Syndrome (SNDNS)

Alias:
Livedo Reticularis-Cerebrovascular Accident Syndrome
Livedo Racemosa-Cerebrovascular Accident Syndrome
Livedo Reticularis and Cerebrovascular Accidents
Ehrmann-Sneddon Syndrome
Sndns
Idiopathic Livedo Reticularis with Systemic Involvement
Sneddon's Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Sneddon Syndrome, also known as livedo reticularis-cerebrovascular accident syndrome, is related to antiphospholipid syndrome and cerebrovascular disease, and has symptoms including headache, hemiplegia and seizures. An important gene associated with Sneddon Syndrome is ADA2 (Adenosine Deaminase 2). Affiliated tissues include skin and bone, and related phenotypes are vascular skin abnormality and vertigo
Related ID:
MESH:D018860
ICD11:1474816492

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
AD
Adult
1-9/1000000
12
61
13

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
No Data Found!
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