Search results for "[genes] FGF8"

32 hits were found for '[genes] FGF8'

# Family MCID Name MIFTS Score
1
P BRS047 Breast Cancer 100 20.801
2
P CRN037 Craniosynostosis 66 18.014
3
P KLL001 Kallmann Syndrome 61 18.014
4
HYP552 Hypogonadotropic Hypogonadism 6 with or Without Anosmia 16 18.014
5
P PRS040 Prostate Cancer 90 16.445
6
P HLP001 Holoprosencephaly 63 16.445
7
P HYP040 Hypospadias 57 16.445
8
HYP080 Hypogonadism 53 16.445
9
P PFF001 Pfeiffer Syndrome 73 14.709
10
PRS045 Prostatic Hypertrophy 45 14.709
11
P THN009 Thanatophoric Dysplasia, Type I 63 12.738
12
CHR103 Charge Syndrome 62 12.738
13
LDD001 Ladd Syndrome 59 12.738
14
AGN012 Agnathia-Otocephaly Complex 53 12.738
15
SNG010 Single Median Maxillary Central Incisor 52 12.738
16
c SPN327 Spinocerebellar Ataxia, Autosomal Recessive 1 48 12.738
17
SML028 Semilobar Holoprosencephaly 37 12.738
18
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 36 12.738
19
ALB014 Alobar Holoprosencephaly 35 12.738
20
LBR025 Lobar Holoprosencephaly 34 12.738
21
SPL039 Split Foot 34 12.738
22
P SPL050 Split Hand-Split Foot Malformation 33 12.738
23
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 29 12.738
24
SPT016 Septopreoptic Holoprosencephaly 29 12.738
25
FGF012 Fgf8-Related Isolated Gonadotropin-Releasing Hormone Deficiency 9 12.738
26
P CNT061 Conotruncal Heart Malformations 62 10.401
27
MNK003 Muenke Syndrome 60 10.401
28
c AXN009 Axenfeld-Rieger Syndrome, Type 1 47 10.401
29
PHY002 Physical Disorder 43 10.401
30
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 29 10.401
31
c DFN029 Deafness, Autosomal Recessive 51 28 10.401
32
c KLL008 Kallmann Syndrome 6 13 10.401