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

28 hits were found for 'iridogoniodysgenesis'

# ++ Fam MCID Name MIFTS Score
1
P IRD006 Iridogoniodysgenesis, Dominant Type 28 6.350
2
IRD005 Iridogoniodysgenesis Type1 11 5.272
3
c IRD007 Iridogoniodysgenesis, Type 1 18 4.962
4
c IRD010 Iridogoniodysgenesis Syndrome 15 4.844
5
IRD004 Iridogoniodysgenesis and Skeletal Anomalies 0 3.313
6
INT189 Interstitial Granulomatous Dermatitis with Arthritis 6 2.711
7
c AXN002 Axenfeld-Rieger Syndrome 57 2.539
8
P AXN003 Axenfeld-Rieger Syndrome Type 1 39 0.347
9
JVN024 Juvenile Hereditary Hemochromatosis 28 0.195
10
HNM001 Hinman's Syndrome 28 0.178
11
c GLC074 Glaucoma 1a, Primary Open Angle 14 0.178
12
ACN002 Acanthosis Nigricans 70 0.159
13
IRS004 Iris Hypoplasia and Glaucoma 22 0.138
14
WST001 West Syndrome 64 0.113
15
P GLC007 Glaucoma 49 0.113
16
P THR090 Thrombocythemia 1 48 0.113
17
P ATS008 Autosomal Dominant Disease 45 0.113
18
c ATX010 Ataxia Neuropathy Spectrum 33 0.113
19
c JVN008 Juvenile Glaucoma 26 0.113
20
c BNG076 Benign Exophthalmos Syndrome 17 0.113
21
OTP003 Oto-Palatal-Digital Syndrome 13 0.113
22
P AMY001 Amyotrophic Lateral Sclerosis 87 0.080
23
AND002 Androgen Insensitivity Syndrome 75 0.080
24
P SHR029 Short Syndrome 55 0.080
25
c GLC030 Glaucoma, Congenital 35 0.080
26
ADS002 Adie Syndrome 32 0.080
27
IRS007 Iris Hypoplasia 25 0.080
28
c PRM032 Primary Congenital Glaucoma 23 0.080