Search results for "iridogoniodysgenesis"

The MalaCard for "iridogoniodysgenesis" has been retired.
Searching MalaCards for entries containing "iridogoniodysgenesis"

24 hits were found for 'iridogoniodysgenesis'

# Family MCID Name MIFTS Score
1
c IRD008 Iridogoniodysgenesis, Type 2 29 9.123
2
P IRD007 Iridogoniodysgenesis, Type 1 23 6.568
3
INT189 Interstitial Granulomatous Dermatitis with Arthritis 19 2.527
4
IRD004 Iridogoniodysgenesis and Skeletal Anomalies 2 2.527
5
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 2.474
6
c AXN009 Axenfeld-Rieger Syndrome, Type 1 47 2.474
7
PTR006 Peters Anomaly 65 0.143
8
P ANR002 Aniridia 64 0.117
9
IRS007 Iris Hypoplasia 25 0.117
10
ECT038 Ectopia Lentis, Familial 20 0.117
11
AND005 Androgen Insensitivity Syndrome, Mild 16 0.117
12
HPT074 Hepatic Adenoma, Somatic 50 0.082
13
APH010 Aphakia, Congenital Primary 44 0.082
14
P ANT026 Anterior Segment Mesenchymal Dysgenesis 42 0.082
15
ATS008 Autosomal Dominant Disease 39 0.082
16
ALR002 Al-Raqad Syndrome 36 0.082
17
P JVN008 Juvenile Glaucoma 36 0.082
18
ADP007 Adie Pupil 34 0.082
19
c PRM032 Primary Congenital Glaucoma 30 0.082
20
c JVN024 Juvenile Hereditary Hemochromatosis 29 0.082
21
HNM002 Hinman Syndrome 25 0.082
22
c ERL012 Early-Onset Glaucoma 25 0.082
23
CRN230 Corneal Opacification and Other Ocular Anomalies 22 0.082
24
ANT067 Anterior Segment Dysgenesis 8 10 0.082