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 36 6.346
2
IRD005 Iridogoniodysgenesis Type1 11 5.268
3
c IRD007 Iridogoniodysgenesis, Type 1 27 4.959
4
c IRD010 Iridogoniodysgenesis Syndrome 16 4.841
5
IRD004 Iridogoniodysgenesis and Skeletal Anomalies 1 3.311
6
INT189 Interstitial Granulomatous Dermatitis with Arthritis 11 2.709
7
c AXN002 Axenfeld-Rieger Syndrome 60 2.537
8
P AXN003 Axenfeld-Rieger Syndrome Type 1 49 0.347
9
P JVN024 Juvenile Hereditary Hemochromatosis 35 0.195
10
P GLC074 Glaucoma 1a, Primary Open Angle 26 0.178
11
ACN002 Acanthosis Nigricans 73 0.159
12
HNM002 Hinman Syndrome 24 0.159
13
IRS004 Iris Hypoplasia and Glaucoma 26 0.138
14
WST001 West Syndrome 64 0.112
15
P GLC007 Glaucoma 58 0.112
16
P THR090 Thrombocythemia 1 54 0.112
17
P ATS008 Autosomal Dominant Disease 46 0.112
18
P ATX010 Ataxia Neuropathy Spectrum 44 0.112
19
SYN053 Syndromic Diarrhea 42 0.112
20
c JVN008 Juvenile Glaucoma 27 0.112
21
c BNG076 Benign Exophthalmos Syndrome 21 0.112
22
OTP003 Oto-Palatal-Digital Syndrome 13 0.112
23
P AMY001 Amyotrophic Lateral Sclerosis 100 0.079
24
AND002 Androgen Insensitivity Syndrome 88 0.079
25
P SHR029 Short Syndrome 49 0.079
26
ADS002 Adie Syndrome 33 0.079
27
c PRM032 Primary Congenital Glaucoma 26 0.079
28
IRS007 Iris Hypoplasia 21 0.079