Search results for "iridogoniodysgenesis"

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

28 hits were found for 'iridogoniodysgenesis'

# Family MCID Name MIFTS Score
1
P IRD006 Iridogoniodysgenesis, Dominant Type 38 6.257
2
IRD005 Iridogoniodysgenesis Type1 11 5.241
3
c IRD007 Iridogoniodysgenesis, Type 1 30 4.847
4
c IRD010 Iridogoniodysgenesis Syndrome 14 4.790
5
IRD004 Iridogoniodysgenesis and Skeletal Anomalies 2 3.315
6
c AXN002 Axenfeld-Rieger Syndrome 66 2.503
7
INT189 Interstitial Granulomatous Dermatitis with Arthritis 16 2.410
8
P GLC007 Glaucoma 60 0.138
9
P AXN003 Axenfeld-Rieger Syndrome Type 1 49 0.138
10
ACN002 Acanthosis Nigricans 69 0.113
11
EYD002 Eye Disease 60 0.113
12
P ATX010 Ataxia Neuropathy Spectrum 41 0.113
13
c JVN024 Juvenile Hereditary Hemochromatosis 38 0.113
14
SYN053 Syndromic Diarrhea 32 0.113
15
IRS007 Iris Hypoplasia 28 0.113
16
c BNG076 Benign Exophthalmos Syndrome 22 0.113
17
OTP003 Oto-Palatal-Digital Syndrome 16 0.113
18
P AMY001 Amyotrophic Lateral Sclerosis 98 0.080
19
P SHR029 Short Syndrome 55 0.080
20
ADS002 Adie Syndrome 35 0.080
21
c JVN008 Juvenile Glaucoma 31 0.080
22
c PRM032 Primary Congenital Glaucoma 31 0.080
23
c ERL012 Early-Onset Glaucoma 31 0.080
24
P GLC074 Glaucoma 1a, Primary Open Angle 29 0.080
25
ECT038 Ectopia Lentis, Familial 28 0.080
26
P ATS008 Autosomal Dominant Disease 28 0.080
27
HNM002 Hinman Syndrome 27 0.080
28
IRS004 Iris Hypoplasia and Glaucoma 15 0.080