Search results for ARFGEF2

28 hits were found for ARFGEF2

# Family MCID Name MIFTS Score
1
P PRV002 Periventricular Nodular Heterotopia 54 7.000
2
PRV020 Periventricular Heterotopia with Microcephaly, Autosomal Recessive 24 5.189
3
P MCR010 Microcephaly 55 3.852
4
P HYD006 Hydrocephalus 66 3.734
5
WST001 West Syndrome 61 3.005
6
VSL002 Visual Epilepsy 57 2.253
7
WLK001 Walker-Warburg Syndrome 63 2.087
8
HYP691 Hypomelanosis of Ito 56 2.087
9
P BND018 Band Heterotopia 53 2.087
10
MLL018 Miller-Dieker Lissencephaly Syndrome 52 2.087
11
c PRM031 Primary Autosomal Recessive Microcephaly 48 2.087
12
PHY002 Physical Disorder 43 2.087
13
NRN016 Neuronal Migration Disorders 40 2.087
14
P VNM004 Van Maldergem Syndrome 29 2.087
15
c CNG031 Congenital Nervous System Abnormality 26 2.087
17
NDL022 Nodular Neuronal Heterotopia 16 0.117
18
c ATR087 Atrial Standstill 1 74 0.083
19
P HNT016 Huntington Disease 72 0.083
20
P DYS154 Dystonia 65 0.083
21
P ENC018 Encephalopathy 61 0.083
22
LNN001 Lennox-Gastaut Syndrome 57 0.083
23
QDR001 Quadriplegia 49 0.083
24
c HYD064 Hydrocephalus, Congenital, 1 47 0.083
25
LCK001 Locked-in Syndrome 46 0.083
26
P HYP265 Hypotonia 42 0.083
27
P CRB088 Cerebral Atrophy 38 0.083
28
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.083
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