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 22 21.417
2
P CNG047 Congenital Fibrosis of the Extraocular Muscles 37 18.100
3
KRN002 Kearns-Sayre Syndrome 60 14.020
4
P STR020 Strabismus 55 14.020
5
P PTS002 Ptosis 56 14.020
6
P SDD001 Sudden Infant Death Syndrome 60 11.448
7
OCL011 Ocular Motility Disease 41 11.448
8
EXT022 Exotropia 37 11.448
9
AMB002 Amblyopia 42 11.448
10
CRN031 Cranial Nerve Disease 39 11.448
11
BRW006 Brown Syndrome 31 11.448
12
FCL011 Facial Nerve Disease 37 11.448
13
PRL014 Paralytic Squint 25 11.448
14
HYP048 Hypotropia 30 11.448
15
c PHX001 Phox2a-Related Congenital Fibrosis of the Extraocular Muscles 7 11.448