|
1
|
(HPO:0000123)
|
Nephritis |
|
|
|
|
18 / 7739
|
|
2
|
(HPO:0000365)
|
Hearing impairment |
|
|
|
|
539 / 7739
|
|
3
|
(HPO:0001875)
|
Neutropenia |
|
|
|
|
83 / 7739
|
|
4
|
(HPO:0007721)
|
Saccular conjunctival aneurysms |
|
|
|
|
1 / 7739
|
|
5
|
(HPO:0007815)
|
Abnormal distribution of retinal arterioles and venules |
|
|
|
|
1 / 7739
|
|
6
|
(HPO:0007866)
|
Retinal infarction |
|
|
|
|
2 / 7739
|
|
7
|
(HPO:0007902)
|
Vitreous hemorrhage |
|
|
|
|
9 / 7739
|
|
8
|
(OMIM)
|
Retinal venous segmental beading |
|
|
|
|
1 / 7739
|
|
9
|
(OMIM)
|
Surface retinal neovascularization |
|
|
|
|
1 / 7739
|
|
10
|
(OMIM)
|
Retinal microaneurysms |
|
|
|
|
1 / 7739
|
|
11
|
(OMIM)
|
Altered retinal vascular permeability with lipid exudation |
|
|
|
|
1 / 7739
|
|
12
|
(OMIM)
|
Focal retinal edema |
|
|
|
|
1 / 7739
|
|
13
|
(OMIM)
|
Chronic hereditary nephritis |
|
|
|
|
1 / 7739
|
|
14
|
(OMIM)
|
Benign neutropenia |
|
|
|
|
1 / 7739
|
|
15
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|