Search results for "[genes] FGF8"

19 hits were found for '[genes] FGF8'

# Family MCID Name MIFTS Score
1
P KLL001 Kallmann Syndrome 60 22.201
2
HYP552 Hypogonadotropic Hypogonadism 6 with or Without Anosmia 11 17.552
3
P HLP001 Holoprosencephaly 65 15.699
4
P HYP040 Hypospadias 54 15.699
5
TRT001 Teratocarcinoma 36 15.699
6
P PRS040 Prostate Cancer 84 11.101
7
P PFF001 Pfeiffer Syndrome 74 11.101
8
PRS045 Prostatic Hypertrophy 35 11.101
9
SPL040 Split Hand 35 11.101
10
SPL039 Split Foot 33 11.101
11
ALB014 Alobar Holoprosencephaly 35 7.849
12
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 34 7.849
13
LBR025 Lobar Holoprosencephaly 34 7.849
14
SML028 Semilobar Holoprosencephaly 33 7.849
15
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 30 7.849
16
MCR173 Microform Holoprosencephaly 29 7.849
17
SPT016 Septopreoptic Holoprosencephaly 29 7.849
18
c KLL008 Kallmann Syndrome 6 9 7.849
19
FGF012 Fgf8-Related Isolated Gonadotropin-Releasing Hormone Deficiency 4 7.849