Search results for foxg1

Showing 25 of 354 hits for foxg1
# Family MCID Name MIFTS Score
1
P FXG001 Foxg1 Syndrome 32 72.320
2
RTT008 Rett Syndrome, Congenital Variant 34 61.762
3
P RTT002 Rett Syndrome 78 31.602
4
FXG002 Foxg1 Syndrome Due to 14q12 Microdeletion 16 26.916
5
P STR020 Strabismus 57 20.967
6
FXG003 Foxg1 Syndrome Due to Intragenic Alteration 3 19.233
7
P MCR010 Microcephaly 59 18.321
8
P OPT006 Optic Nerve Disease 56 16.473
9
c CNG031 Congenital Nervous System Abnormality 32 15.865
10
STR015 Stereotypic Movement Disorder 37 15.865
11
P NRV007 Nervous System Disease 67 15.865
12
HYP265 Hypotonia 46 13.462
13
P LSS002 Lissencephaly 54 11.892
14
P MDL005 Medulloblastoma 76 11.720
15
c PRM212 Primary Microcephaly 39 11.075
16
P HLP001 Holoprosencephaly 66 10.776
17
P NNN008 Noonan Syndrome 1 76 9.569
18
P CRD224 Cardiofaciocutaneous Syndrome 1 70 9.442
19
P CFF008 Coffin-Siris Syndrome 1 64 9.442
20
MTR086 Motor Stereotypies 31 9.189
21
WST001 West Syndrome 64 8.991
22
CHR073 Choreatic Disease 54 8.364
23
LNN001 Lennox-Gastaut Syndrome 57 8.283
24
14Q003 14q11.2 Microduplication Syndrome 14 7.683
25
P PTT014 Pitt-Hopkins Syndrome 60 7.036
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