Search results for "[genes] FGF8"

26 hits were found for '[genes] FGF8'

# Family MCID Name MIFTS Score
1
P BRS047 Breast Cancer 100 20.128
2
P KLL001 Kallmann Syndrome 58 18.635
3
HYP552 Hypogonadotropic Hypogonadism 6 with or Without Anosmia 18 18.635
4
P CRN037 Craniosynostosis 61 17.011
5
P HLP001 Holoprosencephaly 63 15.215
6
P HYP040 Hypospadias 49 15.215
7
P PFF001 Pfeiffer Syndrome 69 13.177
8
PRS045 Prostatic Hypertrophy 43 13.177
9
P PRK057 Parkinson Disease, Late-Onset 69 10.759
10
LDD001 Ladd Syndrome 61 10.759
11
CHR103 Charge Syndrome 59 10.759
12
AGN012 Agnathia-Otocephaly Complex 48 10.759
13
c SPN327 Spinocerebellar Ataxia, Autosomal Recessive 1 43 10.759
14
P PRS013 Prosopagnosia 39 10.759
15
P SPL050 Split Hand-Split Foot Malformation 38 10.759
16
SPL039 Split Foot 31 10.759
17
P CNT061 Conotruncal Heart Malformations 58 7.608
18
ALB014 Alobar Holoprosencephaly 38 7.608
19
SML028 Semilobar Holoprosencephaly 37 7.608
20
LBR025 Lobar Holoprosencephaly 37 7.608
21
PHY002 Physical Disorder 33 7.608
22
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 31 7.608
23
MCR173 Microform Holoprosencephaly 30 7.608
24
SPT016 Septopreoptic Holoprosencephaly 30 7.608
25
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 29 7.608
26
FGF012 Fgf8-Related Isolated Gonadotropin-Releasing Hormone Deficiency 9 7.608