Search results for "[genes] FGF8"

29 hits were found for '[genes] FGF8'

# Family MCID Name MIFTS Score
1
HYP552 Hypogonadotropic Hypogonadism 6 with or Without Anosmia 17 19.753
2
P BRS047 Breast Cancer 100 18.288
3
P KLL001 Kallmann Syndrome 61 16.695
4
HYP080 Hypogonadism 54 16.695
5
P CRN037 Craniosynostosis 66 14.932
6
P PFF001 Pfeiffer Syndrome 73 12.932
7
P HYP040 Hypospadias 58 12.932
8
PRS045 Prostatic Hypertrophy 44 12.932
9
P PRK057 Parkinson Disease, Late-Onset 72 10.559
10
P THN009 Thanatophoric Dysplasia, Type I 62 10.559
11
CHR103 Charge Syndrome 64 10.559
12
LDD001 Ladd Syndrome 60 10.559
13
c SPN327 Spinocerebellar Ataxia, Autosomal Recessive 1 50 10.559
14
AGN012 Agnathia-Otocephaly Complex 53 10.559
15
P PRS013 Prosopagnosia 40 10.559
16
P SPL050 Split Hand-Split Foot Malformation 34 10.559
17
SPL039 Split Foot 32 10.559
18
FGF012 Fgf8-Related Isolated Gonadotropin-Releasing Hormone Deficiency 9 10.559
19
P VLC001 Velocardiofacial Syndrome 64 7.466
20
P CNT061 Conotruncal Heart Malformations 61 7.466
21
SNG010 Single Median Maxillary Central Incisor 52 7.466
22
c KLL008 Kallmann Syndrome 6 13 7.466
23
PHY002 Physical Disorder 43 7.466
24
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 30 7.466
25
SML028 Semilobar Holoprosencephaly 36 7.466
26
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 36 7.466
27
SPT016 Septopreoptic Holoprosencephaly 30 7.466
28
ALB014 Alobar Holoprosencephaly 35 7.466
29
LBR025 Lobar Holoprosencephaly 34 7.466