Search results for "FGFR2"

82 hits were found for 'FGFR2'

# Family MCID Name MIFTS Score
1
BNT003 Bent Bone Dysplasia Syndrome 20 10.184
2
CRZ001 Crouzon Syndrome 78 8.829
3
JCK001 Jackson-Weiss Syndrome 59 8.431
4
APR006 Apert Syndrome 74 7.520
5
P PFF001 Pfeiffer Syndrome 85 7.506
6
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 52 6.763
7
P STH001 Saethre-Chotzen Syndrome 76 5.485
8
LDD001 Ladd Syndrome 64 4.980
9
P CRN037 Craniosynostosis 69 4.759
10
ANT003 Antley-Bixler Syndrome 65 3.890
11
ACH004 Achondroplasia 78 3.842
12
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 16 3.559
13
END057 Endometrial Cancer 80 3.284
14
P BRS047 Breast Cancer 91 3.276
15
SYN005 Synostosis 50 3.219
16
ACN002 Acanthosis Nigricans 63 3.167
17
HYP042 Hypochondroplasia 70 3.137
18
P EXP004 Exophthalmos 54 3.137
19
SCP007 Scaphocephaly, Maxillary Retrusion, and Mental Retardation 12 2.780
20
c PFF007 Pfeiffer Syndrome Type 1 41 2.751
21
CTS039 Cutis Gyrata - Acanthosis Nigricans - Craniosynostosis 21 2.397
22
FGF010 Fgfr2-Related Bent Bone Dysplasia 7 2.349
23
P STM004 Stomach Cancer 68 2.292
24
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 52 2.292
25
GST060 Gastric Cancer, Somatic 51 2.292
26
FML273 Familial Scaphocephaly Syndrome, Mcgillivray Type 14 2.292
27
PLG004 Plagiocephaly 45 2.258
28
HMR015 Humeroradial Synostosis 14 2.258
29
P CLR023 Colorectal Cancer 95 2.218
30
P THN009 Thanatophoric Dysplasia, Type I 70 2.218
31
MNK003 Muenke Syndrome 65 2.218
32
WLL006 Wells Syndrome 62 2.218
33
OST044 Osteoglophonic Dysplasia 58 2.218
34
GLM004 Gliomatosis Cerebri 58 2.218
35
P SYR001 Syringomyelia 57 2.218
36
RDL002 Radioulnar Synostosis 46 2.218
37
ACN010 Acanthoma 45 2.218
38
CYT014 Cytochrome P450 Oxidoreductase Deficiency 40 2.218
39
HYW001 Hay-Wells Syndrome 40 2.218
40
ACR015 Acrocephalosyndactylia 39 2.218
41
P CLR001 Clear Cell Acanthoma 37 2.218
42
FGF001 Fgfr-Related Craniosynostosis Syndromes 33 2.218
43
c SPN106 Spinocerebellar Ataxia 5 49 1.962
44
c STM012 Stomach Cancer, Familial 41 1.661
45
STM011 Stomach Cancer, Childhood 27 1.661
46
CRD019 Cardiocranial Syndrome 31 1.569
47
c PFF009 Pfeiffer Syndrome Type 3 24 1.569
48
c FGF004 Fgfr2-Related Craniosynostosis 11 1.569
49
c PFF008 Pfeiffer Syndrome Type 1, 2 and 3 10 1.569
50
c STH004 Saethre-Chotzen Syndrome, Fgfr2-Related 7 1.569
51
c FGF005 Fgfr2-Related Isolated Coronal Synostosis 4 1.569
52
P FGF006 Fgfr2-Related Lacrimo-Auriculo-Dento-Digital Syndrome 4 1.569
53
ACN011 Acne 61 0.126
54
PRS047 Prostatitis 58 0.126
55
CRN113 Craniosynostosis, Syndromic 13 0.126
56
PRS037 Periostitis 44 0.109
57
P PRS040 Prostate Cancer 97 0.089
58
P SYN001 Syndactyly 50 0.089
59
c FML108 Familial Breast Cancer 34 0.089
60
HDG012 Hodgkin Lymphoma 86 0.063
61
P RNL014 Renal Cell Carcinoma 83 0.063
62
NRL016 Neural Tube Defects 79 0.063
63
P BPL003 Bipolar Disorder 75 0.063
64
THY028 Thyroid Cancer 74 0.063
65
CHL065 Cholangiocarcinoma 68 0.063
66
P THY032 Thyroiditis 65 0.063
67
P PSR002 Psoriasis 62 0.063
68
P HYP040 Hypospadias 62 0.063
69
P ESP024 Esophagitis 62 0.063
70
P ADN016 Adenocarcinoma 57 0.063
71
P BRC006 Brachydactyly 57 0.063
72
PPL002 Papillary Carcinoma 56 0.063
73
P PLY006 Polydactyly 56 0.063
74
PLY012 Polyhydramnios 53 0.063
75
P VSC005 Vesicoureteral Reflux 53 0.063
76
CRV038 Cervical Squamous Cell Carcinoma 52 0.063
77
RTN023 Retinitis 51 0.063
78
NRN002 Neuronitis 42 0.063
79
GST040 Gastric Adenocarcinoma 39 0.063
80
SKL017 Skeletal Dysplasias 35 0.063
81
LNG039 Lung Squamous Cell Carcinoma 35 0.063
82
c EST001 Estrogen-Receptor Positive Breast Cancer 24 0.063