Search results for "[genes] FGFR3"

89 hits were found for '[genes] FGFR3'

# Family MCID Name MIFTS Score
1
ACH004 Achondroplasia 64 22.058
2
HYP042 Hypochondroplasia 55 21.119
3
MNK003 Muenke Syndrome 55 20.136
4
P THN009 Thanatophoric Dysplasia, Type I 62 19.102
5
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 37 19.102
6
CTS022 Catshl Syndrome 23 19.102
7
P CLR023 Colorectal Cancer 96 18.010
8
LDD001 Ladd Syndrome 60 18.010
9
BLD087 Bladder Cancer, Somatic 54 18.010
10
SDD003 Saddan 30 18.010
11
c THN010 Thanatophoric Dysplasia, Type Ii 50 16.847
12
CRZ001 Crouzon Syndrome 70 15.597
13
CRV047 Cervical Cancer, Somatic 65 15.597
14
c MLT019 Multiple Myeloma 77 14.238
15
P STH001 Saethre-Chotzen Syndrome 61 14.238
16
TST021 Testicular Germ Cell Tumor 67 14.238
17
KRT036 Keratosis, Seborrheic, Somatic 44 14.238
18
P CRN037 Craniosynostosis 66 14.238
19
ACN002 Acanthosis Nigricans 59 14.238
20
P ADN016 Adenocarcinoma 69 14.238
21
KRT009 Keratosis 50 14.238
22
P MYL007 Myeloma 52 14.238
23
P PFF001 Pfeiffer Syndrome 73 12.735
24
P HYD006 Hydrocephalus 68 12.735
25
URN008 Urinary Bladder Cancer 64 12.735
26
CHR003 Cherubism 50 12.735
27
P SYN001 Syndactyly 49 12.735
28
P SCL018 Scoliosis 56 12.735
29
DWR001 Dwarfism 42 12.735
30
SKL014 Skeletal Dysplasia 44 12.735
31
EPD053 Epidermal Nevus, Somatic 51 11.029
32
WLF002 Wolf-Hirschhorn Syndrome 50 11.029
33
OST015 Osteochondrodysplasia 54 11.029
34
TRN018 Transitional Cell Carcinoma 56 11.029
35
PLG004 Plagiocephaly 40 11.029
36
SMN007 Seminoma 45 11.029
37
LTM002 Luteoma 29 11.029
38
SYN005 Synostosis 44 11.029
39
DRM003 Dermatosis Papulosa Nigra 32 11.029
40
ATS008 Autosomal Dominant Disease 41 11.029
41
FGF001 Fgfr-Related Craniosynostosis Syndromes 33 11.029
42
c FGF007 Fgfr3-Related Craniosynostosis 12 11.029
43
SDC002 Sed Congenita 44 9.005
44
APR006 Apert Syndrome 66 9.005
45
LRW001 Leri-Weill Dyschondrosteosis 42 9.005
46
P KBK002 Kabuki Syndrome 1 49 9.005
47
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 49 9.005
48
ACR011 Acromesomelic Dysplasia, Maroteaux Type 53 9.005
49
JCK001 Jackson-Weiss Syndrome 50 9.005
50
MTP026 Metaphyseal Chondrodysplasia, Murk Jansen Type 46 9.005
51
OST044 Osteoglophonic Dysplasia 49 9.005
52
c OST080 Osteogenesis Imperfecta, Type Ii 50 9.005
53
P EXP004 Exophthalmos 56 9.005
54
URN020 Urinary Bladder Urothelial Carcinoma 53 9.005
55
CHL056 Cheilitis 48 9.005
56
PLS009 Plasma Cell Neoplasm 47 9.005
57
PLS016 Plasma Cell Leukemia 52 9.005
58
SYN031 Synovial Chondromatosis 44 9.005
59
ACR016 Acromesomelic Dysplasia 33 9.005
60
ACT093 Actinic Cheilitis 38 9.005
61
ACR015 Acrocephalosyndactylia 38 9.005
62
PGM003 Pigmentation Disease 34 9.005
63
NNN005 Non-Invasive Bladder Papillary Urothelial Neoplasm 19 9.005
64
URN011 Urinary Tract Papillary Transitional Cell Benign Neoplasm 18 9.005
65
P ATL001 Atelosteogenesis 36 9.005
66
HMN011 Hemangioma of Intra-Abdominal Structure 23 9.005
67
CHN053 Chondromyxoid Fibroma 38 9.005
68
BLD046 Bladder Papillary Transitional Cell Neoplasm 22 9.005
69
ALC001 Alcohol-Related Birth Defect 25 9.005
70
ADN010 Adenosquamous Cell Lung Carcinoma 41 9.005
71
P CHR342 Chiari Malformation 36 9.005
72
HYP047 Hypertropia 28 9.005
73
CHR010 Chorioangioma 34 9.005
74
P OST028 Osteochondroma 45 9.005
75
BND014 Bone Development Disease 40 9.005
76
SKL009 Skeletal Dysplasia, San Diego Type 8 9.005
77
SKL017 Skeletal Dysplasias 41 9.005
78
SML011 Smoldering Myeloma 30 9.005
79
P FGF008 Fgfr3-Related Isolated Coronal Synostosis 5 9.005
80
SCH063 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 52 6.367
81
BNM001 Bone Marrow Cancer 56 6.367
82
CRV040 Cervix Carcinoma 50 6.367
83
ACT008 Actinic Keratosis 53 6.367
84
GLS001 Gliosarcoma 54 6.367
85
GNT002 Giant Cell Glioblastoma 51 6.367
86
INV005 Inverted Follicular Keratosis 30 6.367
87
ISL062 Isolated Plagiocephaly 20 6.367
88
ISL061 Isolated Brachycephaly 23 6.367
89
c FGF009 Fgfr3-Related Lacrimo-Auriculo-Dento-Digital Syndrome 3 6.367