Search results for "[genes] PHOX2A"

17 hits were found for '[genes] PHOX2A'

# Family MCID Name MIFTS Score
1
c FBR050 Fibrosis of Extraocular Muscles, Congenital, 2 23 22.600
2
TKL001 Tukel Syndrome 34 17.867
3
P SDD001 Sudden Infant Death Syndrome 61 15.981
4
KRN002 Kearns-Sayre Syndrome 61 15.981
5
P STR020 Strabismus 51 15.981
6
P PTS002 Ptosis 51 13.840
7
AMB002 Amblyopia 46 13.840
8
CRN031 Cranial Nerve Disease 40 13.840
9
EXT022 Exotropia 39 13.840
10
OCL011 Ocular Motility Disease 37 13.840
11
FCL011 Facial Nerve Disease 36 13.840
12
BRW006 Brown Syndrome 29 13.840
13
HYP048 Hypotropia 27 13.840
14
PRL014 Paralytic Squint 25 13.840
15
c PHX001 Phox2a-Related Congenital Fibrosis of the Extraocular Muscles 5 13.840
16
CNT097 Central Hypoventilation Syndrome, Congenital 59 11.300
17
MBS002 Moebius Syndrome 47 11.300