Search results for "[genes] FGFR2"

66 hits were found for '[genes] FGFR2'

# Family MCID Name MIFTS Score
1
CRZ001 Crouzon Syndrome 70 24.153
2
P PFF001 Pfeiffer Syndrome 72 23.205
3
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 53 23.205
4
JCK001 Jackson-Weiss Syndrome 50 23.205
5
APR006 Apert Syndrome 67 22.217
6
P BRS047 Breast Cancer 100 18.947
7
BNT003 Bent Bone Dysplasia Syndrome 34 18.947
8
LDD001 Ladd Syndrome 60 17.723
9
P STH001 Saethre-Chotzen Syndrome 60 17.723
10
ANT003 Antley-Bixler Syndrome 51 17.723
11
P CRN037 Craniosynostosis 65 16.409
12
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 21 16.409
13
P PRS040 Prostate Cancer 90 14.979
14
END057 Endometrial Cancer 75 14.979
15
P ADN016 Adenocarcinoma 69 14.979
16
P EXP004 Exophthalmos 54 14.979
17
P SYN001 Syndactyly 48 14.979
18
SYN005 Synostosis 47 14.979
19
ACN011 Acne 65 13.397
20
ACN002 Acanthosis Nigricans 57 13.397
21
P HYP040 Hypospadias 56 13.397
22
LNG039 Lung Squamous Cell Carcinoma 54 13.397
23
SKL014 Skeletal Dysplasia 47 13.397
24
KPS004 Kaposi Sarcoma 72 11.603
25
ACH004 Achondroplasia 64 11.603
26
CLF027 Cleft Palate, Isolated 59 11.603
27
HYP042 Hypochondroplasia 57 11.603
28
BLD087 Bladder Cancer, Somatic 57 11.603
29
GST060 Gastric Cancer, Somatic 53 11.603
30
ANK001 Ankylosis 53 11.603
31
P EST001 Estrogen-Receptor Positive Breast Cancer 50 11.603
32
DYS018 Dysostosis 45 11.603
33
ATS008 Autosomal Dominant Disease 43 11.603
34
c PFF007 Pfeiffer Syndrome Type 1 40 11.603
35
HYW001 Hay-Wells Syndrome 37 11.603
36
HMR015 Humeroradial Synostosis 27 11.603
37
SCP007 Scaphocephaly, Maxillary Retrusion, and Mental Retardation 16 11.603
38
P THN009 Thanatophoric Dysplasia, Type I 65 9.473
39
P PLR004 Pleuropulmonary Blastoma 61 9.473
40
INT079 Intrahepatic Cholangiocarcinoma 59 9.473
41
WLL006 Wells Syndrome 58 9.473
42
MNK003 Muenke Syndrome 53 9.473
43
P PRS049 Persistent Mullerian Duct Syndrome 52 9.473
44
RNP001 Renpenning Syndrome 49 9.473
45
BMF001 Bamforth-Lazarus Syndrome 49 9.473
46
MSN003 Mesenteric Vascular Occlusion 48 9.473
47
ACR015 Acrocephalosyndactylia 44 9.473
48
BND014 Bone Development Disease 44 9.473
49
P CLR001 Clear Cell Acanthoma 41 9.473
50
PLG004 Plagiocephaly 38 9.473
51
HYP047 Hypertropia 35 9.473
52
CYT014 Cytochrome P450 Oxidoreductase Deficiency 32 9.473
53
FGF001 Fgfr-Related Craniosynostosis Syndromes 32 9.473
54
ACN010 Acanthoma 28 9.473
55
c PFF009 Pfeiffer Syndrome Type 3 24 9.473
56
DST095 Distal 10q Deletion Syndrome 22 9.473
57
c PFF008 Pfeiffer Syndrome Type 1, 2 and 3 16 9.473
58
CRV029 Cervical Keratinizing Squamous Cell Carcinoma 10 9.473
59
TTH002 Tooth Agenesis 52 6.699
60
CRD019 Cardiocranial Syndrome 26 6.699
61
FML273 Familial Scaphocephaly Syndrome, Mcgillivray Type 12 6.699
62
c FGF004 Fgfr2-Related Craniosynostosis 11 6.699
63
c STH004 Saethre-Chotzen Syndrome, Fgfr2-Related 8 6.699
64
FGF010 Fgfr2-Related Bent Bone Dysplasia 6 6.699
65
c FGF005 Fgfr2-Related Isolated Coronal Synostosis 4 6.699
66
c FGF006 Fgfr2-Related Lacrimo-Auriculo-Dento-Digital Syndrome 4 6.699