GeDiPNet
☰
Home
Browse
Genes
Diseases
Proteins
SNPs / Variants
Pathways ►
Reactome
KEGG
Analysis
Statistics
Resources
Blogs
Login
Contact Us
Search
Home
/
Diseases
/
Doyne honeycomb retinal dystrophy
Doyne honeycomb retinal dystrophy
Log in to bookmark this disease
Bookmark This Disease
Title
Project / Tag (optional)
Note (optional)
Cancel
Save
Download ▾
Download as CSV
Download as PDF
Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
DOYNE HONEYCOMB RETINAL DYSTROPHY
C1832174
MONDO:0007471
CFH
Unknown
18252232
Disgenet
,
GWAS catalog
Complement and coagulation cascades
Staphylococcus aureus infection
Regulation of Complement cascade
CFI
Unknown
25986072
Disgenet
Complement and coagulation cascades
Staphylococcus aureus infection
Regulation of Complement cascade
All
4
Causal
2
Unknown
2
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
2
CTD
0
HPO
0
GWAS catalog
1
GenCC
0
ClinGen
0
Related Diseases
Diseases that share the most curated genes with Doyne honeycomb retinal dystrophy.
5
View disease cluster →
Thrombotic microangiopathy
2 shared genes
CFI, CFH
Related via 2 shared genes including CFI, CFH.
Atypical hemolytic uremic syndrome
2 shared genes
CFI, CFH
Related via 2 shared genes including CFI, CFH.
PRPH2-related retinopathy
1 shared gene
PRPH2
Related via 1 shared gene including PRPH2.
Factor i deficiency
1 shared gene
CFI
Related via 1 shared gene including CFI.
Congenital hernia of foramen of bochdalek
1 shared gene
EFEMP1
Related via 1 shared gene including EFEMP1.
1
GeDiPNet AI Assistant
Online