Search results for "[genes] FGFR3"

90 hits were found for '[genes] FGFR3'

# Family MCID Name MIFTS Score
1
ACH004 Achondroplasia 66 22.066
2
MNK003 Muenke Syndrome 60 21.126
3
HYP042 Hypochondroplasia 57 21.126
4
P THN009 Thanatophoric Dysplasia, Type I 63 20.143
5
P CLR023 Colorectal Cancer 97 19.110
6
LDD001 Ladd Syndrome 59 19.110
7
BLD087 Bladder Cancer, Somatic 54 18.017
8
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 35 18.017
9
SDD003 Saddan 30 18.017
10
CTS022 Catshl Syndrome 23 18.017
11
c THN010 Thanatophoric Dysplasia, Type Ii 49 16.853
12
P MLT019 Multiple Myeloma 83 15.603
13
CRZ001 Crouzon Syndrome 70 15.603
14
P CRN037 Craniosynostosis 66 15.603
15
CRV047 Cervical Cancer, Somatic 65 15.603
16
P STH001 Saethre-Chotzen Syndrome 60 15.603
17
ACN002 Acanthosis Nigricans 57 15.603
18
P PFF001 Pfeiffer Syndrome 73 14.243
19
P ADN016 Adenocarcinoma 69 14.243
20
TST021 Testicular Germ Cell Tumor 69 14.243
21
P OST005 Osteogenesis Imperfecta 69 14.243
22
EPD053 Epidermal Nevus, Somatic 53 14.243
23
P SYN001 Syndactyly 53 14.243
24
KRT009 Keratosis 52 14.243
25
CHR003 Cherubism 50 14.243
26
DWR001 Dwarfism 47 14.243
27
SKL014 Skeletal Dysplasia 46 14.243
28
SYN005 Synostosis 46 14.243
29
KRT036 Keratosis, Seborrheic, Somatic 45 14.243
30
APR006 Apert Syndrome 67 12.740
31
URN008 Urinary Bladder Cancer 66 12.740
32
PPL022 Papilloma 55 12.740
33
OST015 Osteochondrodysplasia 52 12.740
34
c OST080 Osteogenesis Imperfecta, Type Ii 52 12.740
35
BLD131 Bladder Urothelial Carcinoma 51 12.740
36
WLF002 Wolf-Hirschhorn Syndrome 49 12.740
37
P OST028 Osteochondroma 47 12.740
38
PLY012 Polyhydramnios 47 12.740
39
PRP036 Peripheral T-Cell Lymphoma 45 12.740
40
SKL017 Skeletal Dysplasias 45 12.740
41
LRW001 Leri-Weill Dyschondrosteosis 43 12.740
42
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 42 12.740
43
FGF001 Fgfr-Related Craniosynostosis Syndromes 32 12.740
44
DRM003 Dermatosis Papulosa Nigra 32 12.740
45
LTM002 Luteoma 30 12.740
46
P HYD006 Hydrocephalus 66 11.033
47
SDC002 Sed Congenita 53 11.033
48
SCH063 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 53 11.033
49
ACR011 Acromesomelic Dysplasia, Maroteaux Type 51 11.033
50
GNT002 Giant Cell Glioblastoma 51 11.033
51
JCK001 Jackson-Weiss Syndrome 49 11.033
52
P KBK002 Kabuki Syndrome 1 49 11.033
53
PLS009 Plasma Cell Neoplasm 48 11.033
54
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 47 11.033
55
OST044 Osteoglophonic Dysplasia 47 11.033
56
P PRK001 Porokeratosis 45 11.033
57
MTP026 Metaphyseal Chondrodysplasia, Murk Jansen Type 44 11.033
58
PLG004 Plagiocephaly 43 11.033
59
SYN031 Synovial Chondromatosis 42 11.033
60
ADN010 Adenosquamous Cell Lung Carcinoma 41 11.033
61
BND014 Bone Development Disease 40 11.033
62
PGM003 Pigmentation Disease 39 11.033
63
CHN053 Chondromyxoid Fibroma 37 11.033
64
P ATL001 Atelosteogenesis 36 11.033
65
CHR010 Chorioangioma 33 11.033
66
ALC001 Alcohol-Related Birth Defect 31 11.033
67
HMN011 Hemangioma of Intra-Abdominal Structure 29 11.033
68
HYP047 Hypertropia 28 11.033
69
SML011 Smoldering Myeloma 27 11.033
70
BLD046 Bladder Papillary Transitional Cell Neoplasm 25 11.033
71
ISL062 Isolated Plagiocephaly 24 11.033
72
ISL061 Isolated Brachycephaly 23 11.033
73
SPR018 Spermatocytoma 23 11.033
74
URN011 Urinary Tract Papillary Transitional Cell Benign Neoplasm 21 11.033
75
NNN005 Non-Invasive Bladder Papillary Urothelial Neoplasm 20 11.033
76
SKL009 Skeletal Dysplasia, San Diego Type 8 11.033
77
P FGF008 Fgfr3-Related Isolated Coronal Synostosis 3 11.033
78
c FGF009 Fgfr3-Related Lacrimo-Auriculo-Dento-Digital Syndrome 2 11.033
79
GLS001 Gliosarcoma 55 9.008
80
CRV040 Cervix Carcinoma 53 9.008
81
c DWL002 Dowling-Degos Disease 1 49 9.008
82
c OST135 Osteogenesis Imperfecta, Type I 46 9.008
83
PLS016 Plasma Cell Leukemia 42 9.008
84
CRN245 Craniosynostosis, Philadelphia Type 41 9.008
85
ATS008 Autosomal Dominant Disease 39 9.008
86
P CHR342 Chiari Malformation 38 9.008
87
INV005 Inverted Follicular Keratosis 32 9.008
88
c DFN029 Deafness, Autosomal Recessive 51 28 9.008
89
c ATS342 Autosomal Dominant Nonsyndromic Deafness 6 28 9.008
90
TST010 Testicular Spermatocytic Seminoma 19 9.008