Search results for "[genes] PHOX2A"

15 hits were found for '[genes] PHOX2A'

# Family MCID Name MIFTS Score
1
c FBR050 Fibrosis of Extraocular Muscles, Congenital, 2 23 22.889
2
TKL001 Tukel Syndrome 33 16.185
3
KRN002 Kearns-Sayre Syndrome 59 14.017
4
P PTS002 Ptosis 56 14.017
5
P STR020 Strabismus 53 14.017
6
P SDD001 Sudden Infant Death Syndrome 61 11.444
7
AMB002 Amblyopia 46 11.444
8
CRN031 Cranial Nerve Disease 40 11.444
9
EXT022 Exotropia 39 11.444
10
OCL011 Ocular Motility Disease 38 11.444
11
FCL011 Facial Nerve Disease 38 11.444
12
HYP048 Hypotropia 28 11.444
13
BRW006 Brown Syndrome 26 11.444
14
PRL014 Paralytic Squint 23 11.444
15
c PHX001 Phox2a-Related Congenital Fibrosis of the Extraocular Muscles 6 11.444