Search results for "[genes] FGF8"

29 hits were found for '[genes] FGF8'

# Family MCID Name MIFTS Score
1
P KLL001 Kallmann Syndrome 58 21.208
2
P BRS047 Breast Cancer 100 19.838
3
HYP080 Hypogonadism 47 18.366
4
HYP552 Hypogonadotropic Hypogonadism 6 with or Without Anosmia 21 18.366
5
P CRN037 Craniosynostosis 57 16.766
6
P HLP001 Holoprosencephaly 62 14.996
7
P HYP040 Hypospadias 50 14.996
8
P PFF001 Pfeiffer Syndrome 71 12.987
9
PRS045 Prostatic Hypertrophy 41 12.987
10
c PRK057 Parkinson Disease, Late-Onset 73 10.604
11
CHR103 Charge Syndrome 62 10.604
12
LDD001 Ladd Syndrome 60 10.604
13
AGN012 Agnathia-Otocephaly Complex 48 10.604
14
c SPN327 Spinocerebellar Ataxia, Autosomal Recessive 1 45 10.604
15
P PRS013 Prosopagnosia 38 10.604
16
P SPL050 Split Hand-Split Foot Malformation 38 10.604
17
SPL039 Split Foot 31 10.604
18
CHR084 Chromosomal Disease 30 10.604
19
GND003 Gonadal Disease 28 10.604
20
FGF012 Fgf8-Related Isolated Gonadotropin-Releasing Hormone Deficiency 10 10.604
21
P CNT061 Conotruncal Heart Malformations 59 7.498
22
ALB014 Alobar Holoprosencephaly 34 7.498
23
LBR025 Lobar Holoprosencephaly 32 7.498
24
SML028 Semilobar Holoprosencephaly 32 7.498
25
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 29 7.498
26
MCR173 Microform Holoprosencephaly 28 7.498
27
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 28 7.498
28
SPT016 Septopreoptic Holoprosencephaly 28 7.498
29
c KLL008 Kallmann Syndrome 6 7 7.498