Search results for "iridogoniodysgenesis"

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

30 hits were found for 'iridogoniodysgenesis'

# Family MCID Name MIFTS Score
1
P IRD010 Iridogoniodysgenesis Syndrome 43 8.724
2
c IRD006 Iridogoniodysgenesis, Dominant Type 20 7.008
3
IRD005 Iridogoniodysgenesis Type1 12 5.519
4
c AXN002 Axenfeld-Rieger Syndrome 67 3.582
5
IRD004 Iridogoniodysgenesis and Skeletal Anomalies 2 3.491
6
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.155
7
P AXN003 Axenfeld-Rieger Syndrome Type 1 49 0.110
8
c JVN024 Juvenile Hereditary Hemochromatosis 45 0.110
9
IRS007 Iris Hypoplasia 29 0.110
10
OTP003 Oto-Palatal-Digital Syndrome 17 0.110
11
c AMY001 Amyotrophic Lateral Sclerosis 67 0.078
12
ACN002 Acanthosis Nigricans 63 0.078
13
c AMY077 Amyotrophic Lateral Sclerosis Type 18 60 0.078
14
EYD002 Eye Disease 59 0.078
15
P AMY074 Amyotrophic Lateral Sclerosis Type 14 56 0.078
16
P SPR013 Spiradenoma 56 0.078
17
P SHR029 Short Syndrome 55 0.078
18
P ATX010 Ataxia Neuropathy Spectrum 43 0.078
19
ISL078 Isolated Ectopia Lentis 38 0.078
20
ADS002 Adie Syndrome 35 0.078
21
SYN053 Syndromic Diarrhea 34 0.078
22
P GLC074 Glaucoma 1a, Primary Open Angle 33 0.078
23
c ERL012 Early-Onset Glaucoma 32 0.078
24
c JVN008 Juvenile Glaucoma 32 0.078
25
c PRM032 Primary Congenital Glaucoma 30 0.078
26
P ATS008 Autosomal Dominant Disease 28 0.078
27
HNM002 Hinman Syndrome 28 0.078
28
c BNG076 Benign Exophthalmos Syndrome 22 0.078
29
INT189 Interstitial Granulomatous Dermatitis with Arthritis 16 0.078
30
IRS004 Iris Hypoplasia and Glaucoma 15 0.078