Search results for "FGFR2"

81 hits were found for 'FGFR2'

# Family MCID Name MIFTS Score
1
BNT003 Bent Bone Dysplasia Syndrome 17 10.231
2
CRZ001 Crouzon Syndrome 68 8.910
3
JCK001 Jackson-Weiss Syndrome 52 8.511
4
APR006 Apert Syndrome 66 7.590
5
P PFF001 Pfeiffer Syndrome 74 7.575
6
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 45 6.827
7
P STH001 Saethre-Chotzen Syndrome 67 5.538
8
LDD001 Ladd Syndrome 56 5.028
9
P CRN037 Craniosynostosis 60 4.803
10
ANT003 Antley-Bixler Syndrome 57 3.927
11
ACH004 Achondroplasia 68 3.879
12
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 13 3.593
13
END057 Endometrial Cancer 71 3.314
14
P BRS047 Breast Cancer 90 3.303
15
SYN005 Synostosis 43 3.249
16
ACN002 Acanthosis Nigricans 55 3.197
17
HYP042 Hypochondroplasia 61 3.167
18
P EXP004 Exophthalmos 47 3.167
19
SCP007 Scaphocephaly, Maxillary Retrusion, and Mental Retardation 10 2.807
20
c PFF007 Pfeiffer Syndrome Type 1 35 2.777
21
CTS039 Cutis Gyrata - Acanthosis Nigricans - Craniosynostosis 19 2.418
22
FGF010 Fgfr2-Related Bent Bone Dysplasia 6 2.371
23
P STM004 Stomach Cancer 59 2.314
24
GST060 Gastric Cancer, Somatic 45 2.314
25
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 46 2.314
26
FML273 Familial Scaphocephaly Syndrome, Mcgillivray Type 12 2.314
27
PLG004 Plagiocephaly 39 2.280
28
HMR015 Humeroradial Synostosis 13 2.280
29
P CLR023 Colorectal Cancer 96 2.240
30
P THN009 Thanatophoric Dysplasia, Type I 62 2.240
31
MNK003 Muenke Syndrome 56 2.240
32
WLL006 Wells Syndrome 54 2.240
33
OST044 Osteoglophonic Dysplasia 51 2.240
34
GLM004 Gliomatosis Cerebri 50 2.240
35
P SYR001 Syringomyelia 49 2.240
36
RDL002 Radioulnar Synostosis 40 2.240
37
ACN010 Acanthoma 39 2.240
38
CYT014 Cytochrome P450 Oxidoreductase Deficiency 35 2.240
39
HYW001 Hay-Wells Syndrome 35 2.240
40
ACR015 Acrocephalosyndactylia 32 2.240
41
P CLR001 Clear Cell Acanthoma 31 2.240
42
FGF001 Fgfr-Related Craniosynostosis Syndromes 28 2.240
43
c SPN106 Spinocerebellar Ataxia 5 44 1.978
44
CRD019 Cardiocranial Syndrome 26 1.584
45
c PFF009 Pfeiffer Syndrome Type 3 20 1.584
46
c FGF004 Fgfr2-Related Craniosynostosis 9 1.584
47
c PFF008 Pfeiffer Syndrome Type 1, 2 and 3 7 1.584
48
c STH004 Saethre-Chotzen Syndrome, Fgfr2-Related 5 1.584
49
c FGF005 Fgfr2-Related Isolated Coronal Synostosis 3 1.584
50
P FGF006 Fgfr2-Related Lacrimo-Auriculo-Dento-Digital Syndrome 3 1.584
51
ACN011 Acne 58 0.126
52
PRS047 Prostatitis 51 0.126
53
CRN113 Craniosynostosis, Syndromic 12 0.126
54
PRS037 Periostitis 38 0.109
55
P PRS040 Prostate Cancer 84 0.089
56
P SYN001 Syndactyly 43 0.089
57
c FML108 Familial Breast Cancer 29 0.089
58
HDG012 Hodgkin Lymphoma 79 0.063
59
P RNL014 Renal Cell Carcinoma 83 0.063
60
P BPL003 Bipolar Disorder 65 0.063
61
THY028 Thyroid Cancer 63 0.063
62
c MCL042 Macular Degeneration, Age-Related, 1 72 0.063
63
CHL065 Cholangiocarcinoma 59 0.063
64
P THY032 Thyroiditis 56 0.063
65
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 64 0.063
66
P PSR002 Psoriasis 54 0.063
67
P HYP040 Hypospadias 54 0.063
68
P ESP024 Esophagitis 54 0.063
69
P BRC006 Brachydactyly 49 0.063
70
PPL002 Papillary Carcinoma 49 0.063
71
P ADN016 Adenocarcinoma 49 0.063
72
P PLY006 Polydactyly 48 0.063
73
PLY012 Polyhydramnios 46 0.063
74
P VSC005 Vesicoureteral Reflux 46 0.063
75
RTN023 Retinitis 44 0.063
76
NRN002 Neuronitis 36 0.063
77
CHL028 Childhood Type Dermatomyositis 43 0.063
78
GST040 Gastric Adenocarcinoma 34 0.063
79
SKL017 Skeletal Dysplasias 30 0.063
80
LNG039 Lung Squamous Cell Carcinoma 30 0.063
81
c EST001 Estrogen-Receptor Positive Breast Cancer 20 0.063