Search results for "FGFR2"

87 hits were found for 'FGFR2'

# Family MCID Name MIFTS Score
1
BNT003 Bent Bone Dysplasia Syndrome 18 10.549
2
INF030 Infectious Mononucleosis 84 9.626
3
CRZ001 Crouzon Syndrome 78 8.512
4
JCK001 Jackson-Weiss Syndrome 58 8.300
5
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 57 7.175
6
P STH001 Saethre-Chotzen Syndrome 76 6.057
7
c PFF001 Pfeiffer Syndrome 55 5.752
8
LDD001 Ladd Syndrome 62 4.952
9
c CRN037 Craniosynostosis 70 4.721
10
ACR015 Acrocephalosyndactylia 65 4.150
11
ACH004 Achondroplasia 78 3.821
12
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 25 3.821
13
P BRS047 Breast Cancer 86 3.247
14
P END042 Endometrial Carcinoma 76 3.201
15
c SYN005 Synostosis 54 3.201
16
ANT003 Antley-Bixler Syndrome 56 3.176
17
ACN002 Acanthosis Nigricans 63 3.149
18
HYP042 Hypochondroplasia 69 3.120
19
c THN001 Thanatophoric Dysplasia 62 3.120
20
P EXP004 Exophthalmos 55 3.120
21
SCP007 Scaphocephaly, Maxillary Retrusion, and Mental Retardation 17 3.120
22
P PFF007 Pfeiffer Syndrome Type 1 39 2.735
23
GST053 Gastric Cancer 38 2.336
24
CRZ003 Crouzonodermoskeletal Syndrome 48 2.279
25
PLG004 Plagiocephaly 46 2.246
26
HMR015 Humeroradial Synostosis 9 2.246
27
P CLR023 Colorectal Cancer 77 2.206
28
P STM004 Stomach Cancer 69 2.206
29
MNK003 Muenke Syndrome 63 2.206
30
WLL006 Wells Syndrome 63 2.206
31
P THN004 Thanatophoric Dysplasia Type 1 60 2.206
32
GLM004 Gliomatosis Cerebri 59 2.206
33
OST044 Osteoglophonic Dysplasia 56 2.206
34
P SYR001 Syringomyelia 56 2.206
35
ACN010 Acanthoma 47 2.206
36
RDL002 Radioulnar Synostosis 44 2.206
37
GST060 Gastric Cancer, Somatic 43 2.206
38
CYT014 Cytochrome P450 Oxidoreductase Deficiency 41 2.206
39
P CLR001 Clear Cell Acanthoma 39 2.206
40
FGF001 Fgfr-Related Craniosynostosis Syndromes 34 2.206
41
BRS081 Breast Cancer Susceptibility 53 1.685
42
c END056 Endometrial Cancer, Familial 35 1.560
43
END058 Endometrial Carcinoma, Somatic 34 1.560
44
CRD019 Cardiocranial Syndrome 31 1.560
45
STH002 Saethre-Chotzen Syndrome with Eyelid Anomalies 29 1.560
46
c STM012 Stomach Cancer, Familial 28 1.560
47
STM011 Stomach Cancer, Childhood 26 1.560
48
c PFF009 Pfeiffer Syndrome Type 3 21 1.560
49
c FGF004 Fgfr2-Related Craniosynostosis 12 1.560
50
c PFF008 Pfeiffer Syndrome Type 1, 2 and 3 9 1.560
51
c STH004 Saethre-Chotzen Syndrome, Fgfr2-Related 8 1.560
52
CRN118 Craniosynostosis, Nonspecific 4 1.560
53
c FGF005 Fgfr2-Related Isolated Coronal Synostosis 4 1.560
54
c FGF006 Fgfr2-Related Lacrimo-Auriculo-Dento-Digital Syndrome 4 1.560
55
SCP006 Scaphocephaly and Axenfeld-Rieger Anomaly 4 1.560
56
PRS047 Prostatitis 60 0.125
57
ACN011 Acne 58 0.125
58
CRN113 Craniosynostosis, Syndromic 13 0.125
59
PRS037 Periostitis 44 0.108
60
P PRS040 Prostate Cancer 98 0.089
61
c FML108 Familial Breast Cancer 41 0.089
62
P OVR042 Ovarian Cancer 85 0.063
63
P OST018 Osteosarcoma 82 0.063
64
P BPL003 Bipolar Disorder 77 0.063
65
THY028 Thyroid Cancer 75 0.063
66
CHL065 Cholangiocarcinoma 69 0.063
67
c THY032 Thyroiditis 66 0.063
68
P RNL014 Renal Cell Carcinoma 64 0.063
69
P ESP024 Esophagitis 64 0.063
70
PSR002 Psoriasis 63 0.063
71
PPL002 Papillary Carcinoma 59 0.063
72
P ADN016 Adenocarcinoma 59 0.063
73
c BRC006 Brachydactyly 57 0.063
74
P PLY006 Polydactyly 57 0.063
75
P HYP040 Hypospadias 55 0.063
76
PLY012 Polyhydramnios 54 0.063
77
RTN023 Retinitis 54 0.063
78
MTT005 Matthew-Wood Syndrome 53 0.063
79
P CLF002 Cleft Palate 52 0.063
80
c VSC005 Vesicoureteral Reflux 51 0.063
81
c SYN001 Syndactyly 51 0.063
82
NRN002 Neuronitis 44 0.063
83
GST040 Gastric Adenocarcinoma 41 0.063
84
ESP028 Esophageal Squamous Cell Carcinoma 41 0.063
85
LNG039 Lung Squamous Cell Carcinoma 37 0.063
86
SKL017 Skeletal Dysplasias 36 0.063
87
P EST001 Estrogen-Receptor Positive Breast Cancer 25 0.063