Search results for SH3PXD2B

20 hits were found for SH3PXD2B

# Family MCID Name MIFTS Score
1
FRN039 Frank-Ter Haar Syndrome 41 9.283
2
BRR007 Borrone Di Rocco Crovato Syndrome 7 3.396
3
c CTS045 Cutis Laxa, Autosomal Dominant 1 52 3.250
4
P AXN002 Axenfeld-Rieger Syndrome 58 2.372
5
MGL003 Megalocornea 48 2.298
6
c PNT032 Pontocerebellar Hypoplasia, Type 9 41 2.298
7
c MNT179 Mental Retardation, Autosomal Dominant 21 34 2.298
8
AMT001 Ametropic Amblyopia 27 2.298
9
TYM002 Tympanic Membrane Disease 22 2.298
10
ATS010 Autosomal Recessive Disease 49 0.154
11
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.125
12
HYP748 Hypertelorism 50 0.125
13
P ANT088 Anterior Segment Dysgenesis 49 0.125
14
P NRF023 Neurofibromatosis, Type Ii 77 0.089
15
OTT002 Otitis Media 71 0.089
16
P ORT004 Orthostatic Intolerance 63 0.089
17
c GLC092 Glaucoma, Primary Open Angle 62 0.089
18
P OPN001 Open-Angle Glaucoma 49 0.089
19
c PRM032 Primary Congenital Glaucoma 44 0.089
20
c ERL012 Early-Onset Glaucoma 27 0.089
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