Search results for "[genes] FGFR2"

67 hits were found for '[genes] FGFR2'

# Family MCID Name MIFTS Score
1
CRZ001 Crouzon Syndrome 70 23.961
2
P PFF001 Pfeiffer Syndrome 73 23.021
3
APR006 Apert Syndrome 66 23.021
4
JCK001 Jackson-Weiss Syndrome 49 23.021
5
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 47 23.021
6
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 47 21.015
7
BNT003 Bent Bone Dysplasia Syndrome 36 19.937
8
P BRS047 Breast Cancer 100 18.796
9
P STH001 Saethre-Chotzen Syndrome 59 18.796
10
LDD001 Ladd Syndrome 60 17.582
11
P CRN037 Craniosynostosis 65 16.278
12
P PRS040 Prostate Cancer 89 14.860
13
END057 Endometrial Cancer 75 14.860
14
P ADN016 Adenocarcinoma 69 14.860
15
P EXP004 Exophthalmos 54 14.860
16
P STR020 Strabismus 53 14.860
17
SYN005 Synostosis 45 14.860
18
ACN011 Acne 63 13.291
19
HYP042 Hypochondroplasia 57 13.291
20
ACN002 Acanthosis Nigricans 57 13.291
21
P HYP040 Hypospadias 57 13.291
22
LNG039 Lung Squamous Cell Carcinoma 52 13.291
23
CHL069 Cholesteatoma 51 13.291
24
SKL014 Skeletal Dysplasia 46 13.291
25
SCP007 Scaphocephaly, Maxillary Retrusion, and Mental Retardation 21 13.291
26
ACH004 Achondroplasia 66 11.510
27
P THN009 Thanatophoric Dysplasia, Type I 62 11.510
28
CLF027 Cleft Palate, Isolated 56 11.510
29
INT079 Intrahepatic Cholangiocarcinoma 55 11.510
30
ANK001 Ankylosis 52 11.510
31
CRN245 Craniosynostosis, Philadelphia Type 50 11.510
32
P EST001 Estrogen-Receptor Positive Breast Cancer 48 11.510
33
GST060 Gastric Cancer, Somatic 47 11.510
34
DYS018 Dysostosis 44 11.510
35
RDL002 Radioulnar Synostosis 44 11.510
36
ATS008 Autosomal Dominant Disease 42 11.510
37
c PFF007 Pfeiffer Syndrome Type 1 36 11.510
38
HYW001 Hay-Wells Syndrome 33 11.510
39
LTM002 Luteoma 29 11.510
40
HMR015 Humeroradial Synostosis 25 11.510
41
c PFF011 Pfeiffer Syndrome Type 2 23 11.510
42
c FML108 Familial Breast Cancer 57 9.398
43
WLL006 Wells Syndrome 56 9.398
44
MNK003 Muenke Syndrome 55 9.398
45
RNP001 Renpenning Syndrome 48 9.398
46
OST044 Osteoglophonic Dysplasia 47 9.398
47
P SYR001 Syringomyelia 47 9.398
48
BMF001 Bamforth-Lazarus Syndrome 42 9.398
49
PLG004 Plagiocephaly 42 9.398
50
BND014 Bone Development Disease 42 9.398
51
P CLR001 Clear Cell Acanthoma 37 9.398
52
DYS017 Dysgerminoma of Ovary 34 9.398
53
CHN065 Choanal Atresia, Posterior 33 9.398
54
FGF001 Fgfr-Related Craniosynostosis Syndromes 31 9.398
55
c PFF008 Pfeiffer Syndrome Type 1, 2 and 3 28 9.398
56
ACN010 Acanthoma 28 9.398
57
HYP047 Hypertropia 28 9.398
58
CYT014 Cytochrome P450 Oxidoreductase Deficiency 28 9.398
59
CHR377 Chromosome 10q26 Deletion Syndrome 28 9.398
60
c PFF009 Pfeiffer Syndrome Type 3 22 9.398
61
c CNT026 Central Corneal Ulcer 19 9.398
62
c FGF004 Fgfr2-Related Craniosynostosis 11 9.398
63
CRV029 Cervical Keratinizing Squamous Cell Carcinoma 9 9.398
64
TTH002 Tooth Agenesis 55 6.646
65
c STH004 Saethre-Chotzen Syndrome, Fgfr2-Related 5 6.646
66
c FGF005 Fgfr2-Related Isolated Coronal Synostosis 2 6.646
67
c FGF006 Fgfr2-Related Lacrimo-Auriculo-Dento-Digital Syndrome 2 6.646