Search results for "[genes] FGFR2"

69 hits were found for '[genes] FGFR2'

# Family MCID Name MIFTS Score
1
CRZ001 Crouzon Syndrome 70 23.864
2
P PFF001 Pfeiffer Syndrome 73 22.928
3
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 49 22.928
4
JCK001 Jackson-Weiss Syndrome 50 22.928
5
APR006 Apert Syndrome 66 21.952
6
BNT003 Bent Bone Dysplasia Syndrome 37 19.856
7
P BRS047 Breast Cancer 100 18.721
8
P STH001 Saethre-Chotzen Syndrome 61 18.721
9
LDD001 Ladd Syndrome 60 17.512
10
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 28 17.512
11
P PRS040 Prostate Cancer 89 14.800
12
END057 Endometrial Cancer 75 14.800
13
P CRN037 Craniosynostosis 66 14.800
14
ANT003 Antley-Bixler Syndrome 43 14.800
15
P ADN016 Adenocarcinoma 69 14.800
16
ACN011 Acne 63 13.238
17
HYP042 Hypochondroplasia 55 13.238
18
P EXP004 Exophthalmos 56 13.238
19
SCP007 Scaphocephaly, Maxillary Retrusion, and Mental Retardation 22 13.238
20
P SYN001 Syndactyly 49 13.238
21
LNG039 Lung Squamous Cell Carcinoma 51 13.238
22
SYN005 Synostosis 44 13.238
23
KPS004 Kaposi Sarcoma 69 11.464
24
P THN009 Thanatophoric Dysplasia, Type I 62 11.464
25
ACH004 Achondroplasia 64 11.464
26
CLF027 Cleft Palate, Isolated 56 11.464
27
P STR020 Strabismus 55 11.464
28
BLD087 Bladder Cancer, Somatic 54 11.464
29
ACN002 Acanthosis Nigricans 59 11.464
30
CHL069 Cholesteatoma 51 11.464
31
GST060 Gastric Cancer, Somatic 44 11.464
32
HYW001 Hay-Wells Syndrome 33 11.464
33
RDL002 Radioulnar Synostosis 45 11.464
34
INT079 Intrahepatic Cholangiocarcinoma 55 11.464
35
ANK001 Ankylosis 52 11.464
36
DYS018 Dysostosis 43 11.464
37
LTM002 Luteoma 29 11.464
38
HMR015 Humeroradial Synostosis 24 11.464
39
c PFF007 Pfeiffer Syndrome Type 1 35 11.464
40
ATS008 Autosomal Dominant Disease 41 11.464
41
c PFF011 Pfeiffer Syndrome Type 2 21 11.464
42
P EST001 Estrogen-Receptor Positive Breast Cancer 47 11.464
43
RNP001 Renpenning Syndrome 48 9.360
44
MNK003 Muenke Syndrome 55 9.360
45
OST044 Osteoglophonic Dysplasia 49 9.360
46
P PRS049 Persistent Mullerian Duct Syndrome 52 9.360
47
WLL006 Wells Syndrome 57 9.360
48
BMF001 Bamforth-Lazarus Syndrome 43 9.360
49
P SYR001 Syringomyelia 44 9.360
50
CHL122 Cholesteatoma of Middle Ear 32 9.360
51
PLG004 Plagiocephaly 40 9.360
52
DST095 Distal 10q Deletion Syndrome 22 9.360
53
ACN010 Acanthoma 29 9.360
54
DYS017 Dysgerminoma of Ovary 33 9.360
55
P CLR001 Clear Cell Acanthoma 37 9.360
56
ACR015 Acrocephalosyndactylia 38 9.360
57
CYT014 Cytochrome P450 Oxidoreductase Deficiency 28 9.360
58
HYP047 Hypertropia 28 9.360
59
c FGF004 Fgfr2-Related Craniosynostosis 11 9.360
60
BND014 Bone Development Disease 40 9.360
61
c PFF008 Pfeiffer Syndrome Type 1, 2 and 3 11 9.360
62
CRV029 Cervical Keratinizing Squamous Cell Carcinoma 8 9.360
63
FGF001 Fgfr-Related Craniosynostosis Syndromes 33 9.360
64
c PFF009 Pfeiffer Syndrome Type 3 20 9.360
65
TTH002 Tooth Agenesis 54 6.619
66
c FML108 Familial Breast Cancer 58 6.619
67
c FGF005 Fgfr2-Related Isolated Coronal Synostosis 3 6.619
68
c FGF006 Fgfr2-Related Lacrimo-Auriculo-Dento-Digital Syndrome 3 6.619
69
c STH004 Saethre-Chotzen Syndrome, Fgfr2-Related 5 6.619