Search results for "[genes] FGFR2"

77 hits were found for '[genes] FGFR2'

# Family MCID Name MIFTS Score
1
CRZ001 Crouzon Syndrome 67 24.480
2
P PFF001 Pfeiffer Syndrome 71 23.589
3
JCK001 Jackson-Weiss Syndrome 49 22.664
4
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 47 22.664
5
P BRS047 Breast Cancer 100 21.699
6
APR006 Apert Syndrome 63 21.699
7
SYN005 Synostosis 41 19.628
8
LDD001 Ladd Syndrome 60 18.505
9
P CRN037 Craniosynostosis 57 18.505
10
ANT003 Antley-Bixler Syndrome 50 18.505
11
BNT003 Bent Bone Dysplasia Syndrome 35 18.505
12
P STH001 Saethre-Chotzen Syndrome 65 17.310
13
CNN005 Connective Tissue Disease 49 17.310
14
DYS018 Dysostosis 43 17.310
15
P PRS040 Prostate Cancer 90 16.026
16
ATS008 Autosomal Dominant Disease 31 16.026
17
BND014 Bone Development Disease 28 16.026
18
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 24 16.026
19
END057 Endometrial Cancer 67 14.630
20
P STM004 Stomach Cancer 63 14.630
21
P ADN016 Adenocarcinoma 56 14.630
22
P SYN001 Syndactyly 49 14.630
23
P THR012 Thoracic Cancer 44 14.630
24
P EXP004 Exophthalmos 44 14.630
25
ATS009 Autosomal Genetic Disease 28 14.630
26
BLD087 Bladder Cancer, Somatic 58 13.085
27
HYP042 Hypochondroplasia 56 13.085
28
ACN011 Acne 55 13.085
29
ACN002 Acanthosis Nigricans 53 13.085
30
P HYP040 Hypospadias 50 13.085
31
P STR020 Strabismus 47 13.085
32
CHL069 Cholesteatoma 43 13.085
33
LNG039 Lung Squamous Cell Carcinoma 41 13.085
34
SKL014 Skeletal Dysplasia 38 13.085
35
ACR015 Acrocephalosyndactylia 31 13.085
36
KPS004 Kaposi Sarcoma 65 11.332
37
ACH004 Achondroplasia 65 11.332
38
P THN009 Thanatophoric Dysplasia, Type I 61 11.332
39
CLF027 Cleft Palate, Isolated 52 11.332
40
GST060 Gastric Cancer, Somatic 48 11.332
41
ANK001 Ankylosis 43 11.332
42
P EST001 Estrogen-Receptor Positive Breast Cancer 37 11.332
43
HYW001 Hay-Wells Syndrome 37 11.332
44
RDL002 Radioulnar Synostosis 35 11.332
45
c PFF007 Pfeiffer Syndrome Type 1 30 11.332
46
LTM002 Luteoma 30 11.332
47
SCP007 Scaphocephaly, Maxillary Retrusion, and Mental Retardation 20 11.332
48
FGF010 Fgfr2-Related Bent Bone Dysplasia 7 11.332
49
MNK003 Muenke Syndrome 54 9.253
50
RNP001 Renpenning Syndrome 50 9.253
51
WLL006 Wells Syndrome 48 9.253
52
OST044 Osteoglophonic Dysplasia 47 9.253
53
P TMR015 Tumoral Calcinosis 44 9.253
54
PRK001 Porokeratosis 44 9.253
55
BMF001 Bamforth-Lazarus Syndrome 44 9.253
56
P SYR001 Syringomyelia 39 9.253
57
ACN010 Acanthoma 38 9.253
58
MSN003 Mesenteric Vascular Occlusion 35 9.253
59
P CLR001 Clear Cell Acanthoma 35 9.253
60
PLG004 Plagiocephaly 33 9.253
61
MLR006 Male Reproductive Organ Cancer 33 9.253
62
HYP047 Hypertropia 31 9.253
63
CYT014 Cytochrome P450 Oxidoreductase Deficiency 29 9.253
64
FGF001 Fgfr-Related Craniosynostosis Syndromes 24 9.253
65
CTS039 Cutis Gyrata - Acanthosis Nigricans - Craniosynostosis 19 9.253
66
HMR015 Humeroradial Synostosis 13 9.253
67
FML273 Familial Scaphocephaly Syndrome, Mcgillivray Type 12 9.253
68
CRV029 Cervical Keratinizing Squamous Cell Carcinoma 5 9.253
69
TTH002 Tooth Agenesis 48 6.543
70
c SPN106 Spinocerebellar Ataxia 5 43 6.543
71
CRD019 Cardiocranial Syndrome 26 6.543
72
c PFF009 Pfeiffer Syndrome Type 3 21 6.543
73
c PFF008 Pfeiffer Syndrome Type 1, 2 and 3 13 6.543
74
c FGF004 Fgfr2-Related Craniosynostosis 9 6.543
75
c STH004 Saethre-Chotzen Syndrome, Fgfr2-Related 7 6.543
76
c FGF005 Fgfr2-Related Isolated Coronal Synostosis 4 6.543
77
c FGF006 Fgfr2-Related Lacrimo-Auriculo-Dento-Digital Syndrome 4 6.543