Search results for "[genes] FGFR2"

66 hits were found for '[genes] FGFR2'

# Family MCID Name MIFTS Score
1
CRZ001 Crouzon Syndrome 66 24.153
2
P PFF001 Pfeiffer Syndrome 69 23.205
3
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 54 23.205
4
JCK001 Jackson-Weiss Syndrome 51 23.205
5
APR006 Apert Syndrome 63 22.217
6
P BRS047 Breast Cancer 100 18.947
7
BNT003 Bent Bone Dysplasia Syndrome 34 18.947
8
P STH001 Saethre-Chotzen Syndrome 62 17.723
9
LDD001 Ladd Syndrome 61 17.723
10
ANT003 Antley-Bixler Syndrome 51 17.723
11
P CRN037 Craniosynostosis 61 16.409
12
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 24 16.409
13
P PRS040 Prostate Cancer 87 14.979
14
END057 Endometrial Cancer 73 14.979
15
P ADN016 Adenocarcinoma 59 14.979
16
P SYN001 Syndactyly 48 14.979
17
SYN005 Synostosis 42 14.979
18
P EXP004 Exophthalmos 42 14.979
19
ACN011 Acne 55 13.397
20
ACN002 Acanthosis Nigricans 50 13.397
21
P HYP040 Hypospadias 49 13.397
22
LNG039 Lung Squamous Cell Carcinoma 45 13.397
23
SKL014 Skeletal Dysplasia 40 13.397
24
KPS004 Kaposi Sarcoma 66 11.603
25
ACH004 Achondroplasia 65 11.603
26
HYP042 Hypochondroplasia 57 11.603
27
CLF027 Cleft Palate, Isolated 53 11.603
28
BLD087 Bladder Cancer, Somatic 51 11.603
29
GST060 Gastric Cancer, Somatic 45 11.603
30
ANK001 Ankylosis 42 11.603
31
P EST001 Estrogen-Receptor Positive Breast Cancer 41 11.603
32
DYS018 Dysostosis 38 11.603
33
HYW001 Hay-Wells Syndrome 36 11.603
34
ATS008 Autosomal Dominant Disease 34 11.603
35
c PFF007 Pfeiffer Syndrome Type 1 34 11.603
36
HMR015 Humeroradial Synostosis 26 11.603
37
SCP007 Scaphocephaly, Maxillary Retrusion, and Mental Retardation 20 11.603
38
P THN009 Thanatophoric Dysplasia, Type I 62 9.473
39
P PRS049 Persistent Mullerian Duct Syndrome 56 9.473
40
P PLR004 Pleuropulmonary Blastoma 55 9.473
41
MNK003 Muenke Syndrome 55 9.473
42
INT079 Intrahepatic Cholangiocarcinoma 48 9.473
43
WLL006 Wells Syndrome 46 9.473
44
RNP001 Renpenning Syndrome 46 9.473
45
BMF001 Bamforth-Lazarus Syndrome 43 9.473
46
P CLR001 Clear Cell Acanthoma 40 9.473
47
MSN003 Mesenteric Vascular Occlusion 40 9.473
48
PLG004 Plagiocephaly 37 9.473
49
ACR015 Acrocephalosyndactylia 35 9.473
50
BND014 Bone Development Disease 33 9.473
51
HYP047 Hypertropia 30 9.473
52
CYT014 Cytochrome P450 Oxidoreductase Deficiency 29 9.473
53
FGF001 Fgfr-Related Craniosynostosis Syndromes 29 9.473
54
ACN010 Acanthoma 27 9.473
55
DST095 Distal 10q Deletion Syndrome 19 9.473
56
c PFF009 Pfeiffer Syndrome Type 3 18 9.473
57
c PFF008 Pfeiffer Syndrome Type 1, 2 and 3 11 9.473
58
CRV029 Cervical Keratinizing Squamous Cell Carcinoma 5 9.473
59
TTH002 Tooth Agenesis 51 6.699
60
CRD019 Cardiocranial Syndrome 27 6.699
61
FML273 Familial Scaphocephaly Syndrome, Mcgillivray Type 11 6.699
62
c FGF004 Fgfr2-Related Craniosynostosis 9 6.699
63
FGF010 Fgfr2-Related Bent Bone Dysplasia 6 6.699
64
c STH004 Saethre-Chotzen Syndrome, Fgfr2-Related 5 6.699
65
c FGF005 Fgfr2-Related Isolated Coronal Synostosis 3 6.699
66
c FGF006 Fgfr2-Related Lacrimo-Auriculo-Dento-Digital Syndrome 3 6.699