Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy (CHAPLE)
Alias:
Chaple
Complement Hyperactivation-Angiopathic Thrombosis-Protein-Losing Enteropathy Syndrome
Protein-Losing Enteropathy
Thrombosis of Blood Vessel
Cd55 Deficiency
Chaple Syndrome
Thrombosis
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy, also known as chaple, is related to congenital disorder of glycosylation, type ib and congenital diarrhea 7 with exudative enteropathy. An important gene associated with Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy is CD55 (CD55 Molecule (Cromer Blood Group)). The drugs Abciximab and Alprostadil have been mentioned in the context of this disorder. Affiliated tissues include liver and heart, and related phenotypes are malabsorption and decreased circulating antibody level
Related ID:
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Infant
<1/1000000
1
10
3
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
#
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
Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Sources
Back to top