Search results for "FGFR2"

80 hits were found for 'FGFR2'

# Family MCID Name MIFTS Score
1
BNT003 Bent Bone Dysplasia Syndrome 18 10.235
2
INF030 Infectious Mononucleosis 84 9.862
3
CRZ001 Crouzon Syndrome 77 8.194
4
JCK001 Jackson-Weiss Syndrome 57 7.985
5
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 55 6.901
6
P STH001 Saethre-Chotzen Syndrome 75 5.629
7
LDD001 Ladd Syndrome 61 5.141
8
c CRN037 Craniosynostosis 70 4.896
9
ACR015 Acrocephalosyndactylia 65 3.992
10
ACH004 Achondroplasia 78 3.967
11
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 25 3.622
12
P BRS047 Breast Cancer 100 3.340
13
c SYN005 Synostosis 54 3.322
14
ANT003 Antley-Bixler Syndrome 56 3.297
15
ACN002 Acanthosis Nigricans 69 3.269
16
HYP042 Hypochondroplasia 69 3.239
17
c THN001 Thanatophoric Dysplasia 61 3.239
18
P EXP004 Exophthalmos 54 3.239
19
P PFF007 Pfeiffer Syndrome Type 1 38 2.839
20
SCP007 Scaphocephaly, Maxillary Retrusion, and Mental Retardation 17 2.805
21
CRZ003 Crouzonodermoskeletal Syndrome 47 2.365
22
PLG004 Plagiocephaly 45 2.331
23
ISL029 Isolated Anorectal Malformation 15 2.331
24
HMR015 Humeroradial Synostosis 6 2.331
25
P CLR023 Colorectal Cancer 73 2.290
26
MNK003 Muenke Syndrome 63 2.290
27
WLL006 Wells Syndrome 62 2.290
28
P SYR001 Syringomyelia 60 2.290
29
P THN004 Thanatophoric Dysplasia Type 1 59 2.290
30
GLM004 Gliomatosis Cerebri 58 2.290
31
OST044 Osteoglophonic Dysplasia 55 2.290
32
ACN010 Acanthoma 46 2.290
33
RDL002 Radioulnar Synostosis 43 2.290
34
CYT014 Cytochrome P450 Oxidoreductase Deficiency 39 2.290
35
P CLR001 Clear Cell Acanthoma 38 2.290
36
FGF001 Fgfr-Related Craniosynostosis Syndromes 33 2.290
37
BRS081 Breast Cancer Susceptibility 54 1.747
38
GST060 Gastric Cancer, Somatic 50 1.620
39
CRD019 Cardiocranial Syndrome 30 1.620
40
c PFF009 Pfeiffer Syndrome Type 3 21 1.620
41
c FGF004 Fgfr2-Related Craniosynostosis 12 1.620
42
c PFF008 Pfeiffer Syndrome Type 1, 2 and 3 8 1.620
43
c STH004 Saethre-Chotzen Syndrome, Fgfr2-Related 8 1.620
44
CRN118 Craniosynostosis, Nonspecific 4 1.620
45
c FGF005 Fgfr2-Related Isolated Coronal Synostosis 4 1.620
46
c FGF006 Fgfr2-Related Lacrimo-Auriculo-Dento-Digital Syndrome 4 1.620
47
SCP006 Scaphocephaly and Axenfeld-Rieger Anomaly 4 1.620
48
PRS047 Prostatitis 60 0.128
49
CRN113 Craniosynostosis, Syndromic 14 0.128
50
P END042 Endometrial Carcinoma 72 0.111
51
ACN011 Acne 57 0.111
52
PRS037 Periostitis 44 0.111
53
P PRS040 Prostate Cancer 87 0.090
54
P CLF002 Cleft Palate 52 0.090
55
c SYN001 Syndactyly 50 0.090
56
c FML108 Familial Breast Cancer 39 0.090
57
P OVR042 Ovarian Cancer 81 0.064
58
P OST018 Osteosarcoma 79 0.064
59
P BPL003 Bipolar Disorder 75 0.064
60
THY028 Thyroid Cancer 73 0.064
61
CHL065 Cholangiocarcinoma 69 0.064
62
c THY032 Thyroiditis 66 0.064
63
P ESP024 Esophagitis 63 0.064
64
MTT005 Matthew-Wood Syndrome 63 0.064
65
PSR002 Psoriasis 63 0.064
66
P RNL014 Renal Cell Carcinoma 62 0.064
67
PPL002 Papillary Carcinoma 59 0.064
68
P ADN016 Adenocarcinoma 58 0.064
69
P PLY006 Polydactyly 56 0.064
70
c BRC006 Brachydactyly 55 0.064
71
P HYP040 Hypospadias 55 0.064
72
PLY012 Polyhydramnios 54 0.064
73
RTN023 Retinitis 53 0.064
74
c VSC005 Vesicoureteral Reflux 50 0.064
75
NRN002 Neuronitis 43 0.064
76
ESP028 Esophageal Squamous Cell Carcinoma 40 0.064
77
GST040 Gastric Adenocarcinoma 40 0.064
78
SKL017 Skeletal Dysplasias 39 0.064
79
LNG039 Lung Squamous Cell Carcinoma 35 0.064
80
P EST001 Estrogen-Receptor Positive Breast Cancer 24 0.064