Search results for [ge] TAB2

Showing 16 of 16 hits for [ge] TAB2
# Family MCID Name MIFTS Score
1
c CNG511 Congenital Heart Defects, Multiple Types, 2 26 30.472
2
PLY088 Polyvalvular Heart Disease Syndrome 20 19.814
3
c TYP031 Type 1 Diabetes Mellitus 5 48 16.269
4
P HRT032 Heart Disease 80 15.422
5
c ART115 Aortic Valve Disease 1 78 10.905
6
P NNN008 Noonan Syndrome 1 76 10.905
7
P ECT006 Ectodermal Dysplasia 56 10.905
8
P ENC018 Encephalopathy 64 8.558
9
c MGR028 Migraine with or Without Aura 1 67 7.711
10
P PLV020 Pelvic Organ Prolapse 62 7.711
11
ECT061 Ectodermal Dysplasia 10a, Hypohidrotic/hair/nail Type, Autosomal Dominant 49 7.711
12
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 67 7.711
13
P ATR066 Atrial Septal Defect 2 47 7.711
14
P OTP008 Otopalatodigital Syndrome Spectrum Disorder 33 7.711
15
P FRN012 Frontometaphyseal Dysplasia 52 7.711
16
PTN001 Patent Foramen Ovale 63 7.711
1
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