Search results for "[genes] FGFR3"

86 hits were found for '[genes] FGFR3'

# Family MCID Name MIFTS Score
1
ACH004 Achondroplasia 66 22.167
2
HYP042 Hypochondroplasia 57 21.224
3
BLD087 Bladder Cancer, Somatic 67 20.236
4
MNK003 Muenke Syndrome 55 20.236
5
P THN009 Thanatophoric Dysplasia, Type I 62 19.197
6
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 36 19.197
7
P CLR023 Colorectal Cancer 97 18.100
8
LDD001 Ladd Syndrome 60 18.100
9
SDD003 Saddan 30 18.100
10
c THN010 Thanatophoric Dysplasia, Type Ii 49 16.931
11
CTS022 Catshl Syndrome 23 16.931
12
P MLT019 Multiple Myeloma 80 15.675
13
CRZ001 Crouzon Syndrome 70 15.675
14
TST021 Testicular Germ Cell Tumor 70 15.675
15
P ADN016 Adenocarcinoma 69 15.675
16
CRV047 Cervical Cancer, Somatic 65 15.675
17
P CRN037 Craniosynostosis 65 15.675
18
ACN002 Acanthosis Nigricans 57 15.675
19
P STH001 Saethre-Chotzen Syndrome 59 14.309
20
KRT009 Keratosis 50 14.309
21
SKL014 Skeletal Dysplasia 46 14.309
22
DWR001 Dwarfism 46 14.309
23
KRT036 Keratosis, Seborrheic, Somatic 46 14.309
24
P PFF001 Pfeiffer Syndrome 73 12.798
25
P HYD006 Hydrocephalus 67 12.798
26
P SCL018 Scoliosis 56 12.798
27
CHR003 Cherubism 50 12.798
28
SYN005 Synostosis 45 12.798
29
APR006 Apert Syndrome 66 11.084
30
PPL022 Papilloma 55 11.084
31
OST015 Osteochondrodysplasia 53 11.084
32
EPD053 Epidermal Nevus, Somatic 51 11.084
33
BLD129 Bladder Urothelial Carcinoma 50 11.084
34
CRN245 Craniosynostosis, Philadelphia Type 50 11.084
35
P OST028 Osteochondroma 48 11.084
36
PLY012 Polyhydramnios 47 11.084
37
WLF002 Wolf-Hirschhorn Syndrome 45 11.084
38
SKL017 Skeletal Dysplasias 45 11.084
39
PRP036 Peripheral T-Cell Lymphoma 45 11.084
40
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 43 11.084
41
ATS008 Autosomal Dominant Disease 42 11.084
42
PLG004 Plagiocephaly 42 11.084
43
FGF001 Fgfr-Related Craniosynostosis Syndromes 31 11.084
44
DRM003 Dermatosis Papulosa Nigra 31 11.084
45
LTM002 Luteoma 29 11.084
46
ACR011 Acromesomelic Dysplasia, Maroteaux Type 51 9.050
47
c OST080 Osteogenesis Imperfecta, Type Ii 51 9.050
48
JCK001 Jackson-Weiss Syndrome 49 9.050
49
PLS009 Plasma Cell Neoplasm 48 9.050
50
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 47 9.050
51
OST044 Osteoglophonic Dysplasia 47 9.050
52
SDC002 Sed Congenita 45 9.050
53
MTP026 Metaphyseal Chondrodysplasia, Murk Jansen Type 45 9.050
54
P PRK001 Porokeratosis 44 9.050
55
ADN010 Adenosquamous Cell Lung Carcinoma 42 9.050
56
BND014 Bone Development Disease 42 9.050
57
PLS016 Plasma Cell Leukemia 42 9.050
58
PGM003 Pigmentation Disease 42 9.050
59
SYN031 Synovial Chondromatosis 41 9.050
60
LRW001 Leri-Weill Dyschondrosteosis 40 9.050
61
P CHR342 Chiari Malformation 37 9.050
62
CHN053 Chondromyxoid Fibroma 37 9.050
63
P ATL001 Atelosteogenesis 37 9.050
64
CHR010 Chorioangioma 33 9.050
65
ACR016 Acromesomelic Dysplasia 31 9.050
66
HYP047 Hypertropia 28 9.050
67
SML011 Smoldering Myeloma 27 9.050
68
BLD046 Bladder Papillary Transitional Cell Neoplasm 27 9.050
69
ALC001 Alcohol-Related Birth Defect 26 9.050
70
SPR018 Spermatocytoma 24 9.050
71
HMN011 Hemangioma of Intra-Abdominal Structure 22 9.050
72
URN011 Urinary Tract Papillary Transitional Cell Benign Neoplasm 20 9.050
73
NNN005 Non-Invasive Bladder Papillary Urothelial Neoplasm 20 9.050
74
SKL009 Skeletal Dysplasia, San Diego Type 8 9.050
75
P FGF008 Fgfr3-Related Isolated Coronal Synostosis 5 9.050
76
GLS001 Gliosarcoma 55 6.399
77
ACT008 Actinic Keratosis 53 6.399
78
CRV040 Cervix Carcinoma 53 6.399
79
SCH063 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 52 6.399
80
GNT002 Giant Cell Glioblastoma 51 6.399
81
P KBK002 Kabuki Syndrome 1 49 6.399
82
INV005 Inverted Follicular Keratosis 32 6.399
83
ISL062 Isolated Plagiocephaly 24 6.399
84
ISL061 Isolated Brachycephaly 23 6.399
85
TST010 Testicular Spermatocytic Seminoma 18 6.399
86
c FGF009 Fgfr3-Related Lacrimo-Auriculo-Dento-Digital Syndrome 2 6.399