Search results for "[genes] FGF8"

31 hits were found for '[genes] FGF8'

# Family MCID Name MIFTS Score
1
P BRS047 Breast Cancer 100 19.577
2
HYP552 Hypogonadotropic Hypogonadism 6 with or Without Anosmia 17 19.577
3
P KLL001 Kallmann Syndrome 60 18.125
4
P CRN037 Craniosynostosis 65 16.545
5
HYP080 Hypogonadism 54 16.545
6
P PRS040 Prostate Cancer 89 14.799
7
P HLP001 Holoprosencephaly 62 14.799
8
P HYP040 Hypospadias 57 14.799
9
P PFF001 Pfeiffer Syndrome 73 12.816
10
PRS045 Prostatic Hypertrophy 44 12.816
11
P PRK057 Parkinson Disease, Late-Onset 72 10.464
12
CHR103 Charge Syndrome 64 10.464
13
P THN009 Thanatophoric Dysplasia, Type I 62 10.464
14
LDD001 Ladd Syndrome 60 10.464
15
AGN012 Agnathia-Otocephaly Complex 54 10.464
16
THR009 Thrombocytopenia-Absent Radius Syndrome 54 10.464
17
c SPN327 Spinocerebellar Ataxia, Autosomal Recessive 1 49 10.464
18
FCL010 Focal Epithelial Hyperplasia 48 10.464
19
SPL039 Split Foot 33 10.464
20
P SPL050 Split Hand-Split Foot Malformation 32 10.464
21
FGF012 Fgf8-Related Isolated Gonadotropin-Releasing Hormone Deficiency 8 10.464
22
P CNT061 Conotruncal Heart Malformations 62 7.399
23
SNG010 Single Median Maxillary Central Incisor 53 7.399
24
PHY002 Physical Disorder 44 7.399
25
SML028 Semilobar Holoprosencephaly 35 7.399
26
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 35 7.399
27
ALB014 Alobar Holoprosencephaly 34 7.399
28
LBR025 Lobar Holoprosencephaly 33 7.399
29
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 29 7.399
30
SPT016 Septopreoptic Holoprosencephaly 29 7.399
31
c KLL008 Kallmann Syndrome 6 15 7.399