Search results for "FGFR3"

93 hits were found for 'FGFR3'

# Family MCID Name MIFTS Score
1
ACH004 Achondroplasia 68 9.139
2
HYP042 Hypochondroplasia 61 7.353
3
KRT036 Keratosis, Seborrheic, Somatic 33 5.755
4
EPD053 Epidermal Nevus, Somatic 50 5.617
5
MNK003 Muenke Syndrome 56 5.578
6
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 46 5.578
7
BLD087 Bladder Cancer, Somatic 55 5.564
8
LDD001 Ladd Syndrome 56 5.096
9
P THN009 Thanatophoric Dysplasia, Type I 62 4.391
10
P CRN037 Craniosynostosis 60 4.356
11
c THN010 Thanatophoric Dysplasia, Type Ii 46 4.006
12
CTS022 Catshl Syndrome 20 3.953
13
P MYL007 Myeloma 53 3.940
14
SKL017 Skeletal Dysplasias 30 3.816
15
DWR001 Dwarfism 48 3.787
16
P STH001 Saethre-Chotzen Syndrome 67 3.669
17
SDD003 Saddan 26 3.652
18
c MLT019 Multiple Myeloma 75 3.261
19
ACN002 Acanthosis Nigricans 55 3.194
20
CRZ001 Crouzon Syndrome 68 3.019
21
PPL022 Papilloma 55 2.996
22
TST021 Testicular Germ Cell Tumor 51 2.996
23
KRT009 Keratosis 45 2.996
24
CRV047 Cervical Cancer, Somatic 51 2.996
25
P CLR023 Colorectal Cancer 96 2.970
26
SYN005 Synostosis 43 2.970
27
P OST005 Osteogenesis Imperfecta 77 2.942
28
P PFF001 Pfeiffer Syndrome 74 2.942
29
CHR003 Cherubism 60 2.942
30
P OST028 Osteochondroma 47 2.942
31
P STR020 Strabismus 44 2.942
32
FGF001 Fgfr-Related Craniosynostosis Syndromes 28 2.548
33
c FGF007 Fgfr3-Related Craniosynostosis 11 2.548
34
DRM003 Dermatosis Papulosa Nigra 26 2.118
35
SKL009 Skeletal Dysplasia, San Diego Type 7 2.118
36
APR006 Apert Syndrome 66 2.081
37
JCK001 Jackson-Weiss Syndrome 52 2.081
38
OST044 Osteoglophonic Dysplasia 51 2.081
39
c HRD117 Hereditary Breast Cancer 51 2.081
40
c OST080 Osteogenesis Imperfecta, Type Ii 50 2.081
41
PLY012 Polyhydramnios 46 2.081
42
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 45 2.081
43
LRW001 Leri-Weill Dyschondrosteosis 42 2.081
44
RDL002 Radioulnar Synostosis 40 2.081
45
MNC006 Monoclonal Gammopathy of Uncertain Significance 40 2.081
46
PLG004 Plagiocephaly 39 2.081
47
AST006 Astigmatism 35 2.081
48
ACR015 Acrocephalosyndactylia 32 2.081
49
BLD049 Bladder Transitional Cell Papilloma 14 2.081
50
c ALM001 Al Amyloidosis 56 1.666
51
PLS009 Plasma Cell Neoplasm 44 1.618
52
SPR018 Spermatocytoma 18 1.558
53
MCR074 Micromelic Bone Dysplasia with Cloverleaf Skull 16 1.558
54
TST010 Testicular Spermatocytic Seminoma 6 1.558
55
GLS001 Gliosarcoma 52 1.471
56
GNT002 Giant Cell Glioblastoma 47 1.471
57
ISL061 Isolated Brachycephaly 24 1.471
58
ISL062 Isolated Plagiocephaly 18 1.471
59
P FGF008 Fgfr3-Related Isolated Coronal Synostosis 4 1.471
60
c FGF009 Fgfr3-Related Lacrimo-Auriculo-Dento-Digital Syndrome 3 1.471
61
CHN015 Chondrodysplasia 37 0.132
62
PRS047 Prostatitis 51 0.118
63
P PRS040 Prostate Cancer 84 0.103
64
P BRS047 Breast Cancer 90 0.103
65
MLN008 Melanoma 55 0.084
66
TRN018 Transitional Cell Carcinoma 54 0.084
67
DWN001 Down Syndrome 51 0.084
68
P CRV039 Cervicitis 49 0.084
69
CRN113 Craniosynostosis, Syndromic 12 0.084
70
P LNG032 Lung Cancer 94 0.059
71
P RNL014 Renal Cell Carcinoma 83 0.059
72
P CHR090 Chronic Lymphocytic Leukemia 74 0.059
73
P LKM002 Leukemia 66 0.059
74
SRC014 Sarcoma 61 0.059
75
P GLB002 Glioblastoma 59 0.059
76
P HYP004 Hypercalcemia 57 0.059
77
WLD002 Waldenstrom Macroglobulinemia 56 0.059
78
DNG003 Dengue Disease 64 0.059
79
HPT022 Hepatoblastoma 53 0.059
80
HYP266 Hypoxia 49 0.059
81
P BRC006 Brachydactyly 49 0.059
82
MCR004 Macroglobulinemia 48 0.059
83
P GNT008 Giant Cell Tumor 47 0.059
84
ORL011 Oral Cancer 47 0.059
85
RNL078 Renal Dysplasia 46 0.059
86
P CLR108 Colorectal Adenoma 49 0.059
87
OST015 Osteochondrodysplasia 38 0.059
88
FCL014 Focal Epilepsy 37 0.059
89
P RNL017 Renal Oncocytoma 43 0.059
90
ORL015 Oral Squamous Cell Carcinoma 33 0.059
91
CRB009 Cerebritis 33 0.059
92
ADN002 Adenoiditis 31 0.059
93
LNG039 Lung Squamous Cell Carcinoma 30 0.059