Search results for "[genes] FGFR2"

72 hits were found for '[genes] FGFR2'

# Family MCID Name MIFTS Score
1
CRZ001 Crouzon Syndrome 70 23.762
2
P PFF001 Pfeiffer Syndrome 73 22.829
3
APR006 Apert Syndrome 67 22.829
4
JCK001 Jackson-Weiss Syndrome 49 22.829
5
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 47 22.829
6
P BRS047 Breast Cancer 100 19.771
7
P STH001 Saethre-Chotzen Syndrome 60 18.640
8
LDD001 Ladd Syndrome 59 18.640
9
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 43 18.640
10
BNT003 Bent Bone Dysplasia Syndrome 37 18.640
11
SCP007 Scaphocephaly, Maxillary Retrusion, and Mental Retardation 22 17.436
12
P PRS040 Prostate Cancer 90 16.143
13
P ADN016 Adenocarcinoma 69 16.143
14
P CRN037 Craniosynostosis 66 16.143
15
ANT003 Antley-Bixler Syndrome 48 16.143
16
END057 Endometrial Cancer 75 14.736
17
SQM006 Squamous Cell Carcinoma 70 14.736
18
ACN011 Acne 62 14.736
19
P HYP040 Hypospadias 57 14.736
20
HYP042 Hypochondroplasia 57 14.736
21
LNG039 Lung Squamous Cell Carcinoma 54 14.736
22
P EXP004 Exophthalmos 53 14.736
23
P SYN001 Syndactyly 53 14.736
24
P STR020 Strabismus 51 14.736
25
CHL069 Cholesteatoma 49 14.736
26
GST060 Gastric Cancer, Somatic 47 14.736
27
SYN005 Synostosis 46 14.736
28
ACH004 Achondroplasia 66 13.181
29
P THN009 Thanatophoric Dysplasia, Type I 63 13.181
30
MNK003 Muenke Syndrome 60 13.181
31
ACN002 Acanthosis Nigricans 57 13.181
32
INT079 Intrahepatic Cholangiocarcinoma 56 13.181
33
CLF027 Cleft Palate, Isolated 55 13.181
34
P EST001 Estrogen-Receptor Positive Breast Cancer 48 13.181
35
SKL014 Skeletal Dysplasia 46 13.181
36
DYS018 Dysostosis 44 13.181
37
RDL002 Radioulnar Synostosis 44 13.181
38
c PFF007 Pfeiffer Syndrome Type 1 36 13.181
39
HYW001 Hay-Wells Syndrome 32 13.181
40
LTM002 Luteoma 30 13.181
41
HMR015 Humeroradial Synostosis 26 13.181
42
c PFF011 Pfeiffer Syndrome Type 2 23 13.181
43
WLL006 Wells Syndrome 59 11.415
44
c FML108 Familial Breast Cancer 57 11.415
45
ANK001 Ankylosis 51 11.415
46
RNP001 Renpenning Syndrome 47 11.415
47
OST044 Osteoglophonic Dysplasia 47 11.415
48
P SYR001 Syringomyelia 47 11.415
49
PLG004 Plagiocephaly 43 11.415
50
BMF001 Bamforth-Lazarus Syndrome 42 11.415
51
BND014 Bone Development Disease 40 11.415
52
P CLR001 Clear Cell Acanthoma 37 11.415
53
CHN065 Choanal Atresia, Posterior 35 11.415
54
DYS017 Dysgerminoma of Ovary 33 11.415
55
FGF001 Fgfr-Related Craniosynostosis Syndromes 32 11.415
56
ACN010 Acanthoma 31 11.415
57
CHR377 Chromosome 10q26 Deletion Syndrome 29 11.415
58
c PFF008 Pfeiffer Syndrome Type 1, 2 and 3 28 11.415
59
HYP047 Hypertropia 28 11.415
60
CYT014 Cytochrome P450 Oxidoreductase Deficiency 27 11.415
61
c PFF009 Pfeiffer Syndrome Type 3 22 11.415
62
c CNT026 Central Corneal Ulcer 18 11.415
63
c FGF004 Fgfr2-Related Craniosynostosis 11 11.415
64
CRV029 Cervical Keratinizing Squamous Cell Carcinoma 9 11.415
65
c STH004 Saethre-Chotzen Syndrome, Fgfr2-Related 5 11.415
66
c FGF005 Fgfr2-Related Isolated Coronal Synostosis 2 11.415
67
c FGF006 Fgfr2-Related Lacrimo-Auriculo-Dento-Digital Syndrome 2 11.415
68
TTH002 Tooth Agenesis 54 9.320
69
P PRS049 Persistent Mullerian Duct Syndrome 50 9.320
70
CRN245 Craniosynostosis, Philadelphia Type 41 9.320
71
ATS008 Autosomal Dominant Disease 39 9.320
72
PRL006 Paralytic Lagophthalmos 16 9.320