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 61 18.635
3
HYP552 Hypogonadotropic Hypogonadism 6 with or Without Anosmia 19 18.635
4
P CRN037 Craniosynostosis 65 17.011
5
P HLP001 Holoprosencephaly 63 15.215
6
P HYP040 Hypospadias 56 15.215
7
P PFF001 Pfeiffer Syndrome 72 13.177
8
PRS045 Prostatic Hypertrophy 51 13.177
9
P PRK057 Parkinson Disease, Late-Onset 74 10.759
10
CHR103 Charge Syndrome 62 10.759
11
LDD001 Ladd Syndrome 60 10.759
12
AGN012 Agnathia-Otocephaly Complex 51 10.759
13
c SPN327 Spinocerebellar Ataxia, Autosomal Recessive 1 47 10.759
14
P PRS013 Prosopagnosia 43 10.759
15
P SPL050 Split Hand-Split Foot Malformation 40 10.759
16
SPL039 Split Foot 37 10.759
17
P CNT061 Conotruncal Heart Malformations 64 7.608
18
PHY002 Physical Disorder 48 7.608
19
ALB014 Alobar Holoprosencephaly 39 7.608
20
SML028 Semilobar Holoprosencephaly 39 7.608
21
LBR025 Lobar Holoprosencephaly 38 7.608
22
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 32 7.608
23
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 32 7.608
24
MCR173 Microform Holoprosencephaly 32 7.608
25
SPT016 Septopreoptic Holoprosencephaly 31 7.608
26
FGF012 Fgf8-Related Isolated Gonadotropin-Releasing Hormone Deficiency 14 7.608