Search results for "[genes] FGFR3"

85 hits were found for '[genes] FGFR3'

# Family MCID Name MIFTS Score
1
ACH004 Achondroplasia 64 22.340
2
HYP042 Hypochondroplasia 57 21.389
3
MNK003 Muenke Syndrome 53 20.394
4
P THN009 Thanatophoric Dysplasia, Type I 65 19.347
5
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 36 19.347
6
LDD001 Ladd Syndrome 60 18.241
7
BLD087 Bladder Cancer, Somatic 57 18.241
8
SDD003 Saddan 30 18.241
9
CTS022 Catshl Syndrome 20 18.241
10
P CLR023 Colorectal Cancer 97 17.063
11
c THN010 Thanatophoric Dysplasia, Type Ii 50 17.063
12
c MLT019 Multiple Myeloma 77 15.797
13
CRZ001 Crouzon Syndrome 70 15.797
14
CRV047 Cervical Cancer, Somatic 67 15.797
15
P CRN037 Craniosynostosis 65 15.797
16
P MYL007 Myeloma 58 15.797
17
ACN002 Acanthosis Nigricans 57 15.797
18
TST021 Testicular Germ Cell Tumor 66 14.421
19
URN008 Urinary Bladder Cancer 62 14.421
20
P STH001 Saethre-Chotzen Syndrome 60 14.421
21
KRT009 Keratosis 53 14.421
22
P SYN001 Syndactyly 48 14.421
23
DWR001 Dwarfism 47 14.421
24
SKL014 Skeletal Dysplasia 47 14.421
25
KRT036 Keratosis, Seborrheic, Somatic 45 14.421
26
EMB004 Embryonal Carcinoma 60 12.898
27
PPL022 Papilloma 59 12.898
28
TRN018 Transitional Cell Carcinoma 58 12.898
29
CHR003 Cherubism 54 12.898
30
P SCL018 Scoliosis 51 12.898
31
SYN005 Synostosis 47 12.898
32
P PFF001 Pfeiffer Syndrome 72 11.170
33
OST015 Osteochondrodysplasia 54 11.170
34
WLF002 Wolf-Hirschhorn Syndrome 53 11.170
35
SKL017 Skeletal Dysplasias 48 11.170
36
PRP036 Peripheral T-Cell Lymphoma 47 11.170
37
EPD053 Epidermal Nevus, Somatic 47 11.170
38
PLY012 Polyhydramnios 46 11.170
39
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 45 11.170
40
ATS008 Autosomal Dominant Disease 43 11.170
41
PLG004 Plagiocephaly 38 11.170
42
FGF001 Fgfr-Related Craniosynostosis Syndromes 32 11.170
43
DRM003 Dermatosis Papulosa Nigra 32 11.170
44
c FGF007 Fgfr3-Related Craniosynostosis 12 11.170
45
APR006 Apert Syndrome 67 9.120
46
c OST080 Osteogenesis Imperfecta, Type Ii 54 9.120
47
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 53 9.120
48
SDC002 Sed Congenita 53 9.120
49
ACR011 Acromesomelic Dysplasia, Maroteaux Type 51 9.120
50
JCK001 Jackson-Weiss Syndrome 50 9.120
51
PLS009 Plasma Cell Neoplasm 50 9.120
52
P KBK002 Kabuki Syndrome 1 49 9.120
53
MSN003 Mesenteric Vascular Occlusion 48 9.120
54
MTP026 Metaphyseal Chondrodysplasia, Murk Jansen Type 48 9.120
55
P OST028 Osteochondroma 47 9.120
56
ADN010 Adenosquamous Cell Lung Carcinoma 46 9.120
57
ACT093 Actinic Cheilitis 45 9.120
58
ACR015 Acrocephalosyndactylia 44 9.120
59
PLS016 Plasma Cell Leukemia 44 9.120
60
BND014 Bone Development Disease 44 9.120
61
PGM003 Pigmentation Disease 41 9.120
62
P ATL001 Atelosteogenesis 36 9.120
63
HYP047 Hypertropia 35 9.120
64
ACR016 Acromesomelic Dysplasia 35 9.120
65
SML011 Smoldering Myeloma 34 9.120
66
P CHR342 Chiari Malformation 34 9.120
67
CHR010 Chorioangioma 34 9.120
68
ALC001 Alcohol-Related Birth Defect 28 9.120
69
BLD046 Bladder Papillary Transitional Cell Neoplasm 27 9.120
70
HMN011 Hemangioma of Intra-Abdominal Structure 26 9.120
71
URN011 Urinary Tract Papillary Transitional Cell Benign Neoplasm 23 9.120
72
NNN005 Non-Invasive Bladder Papillary Urothelial Neoplasm 20 9.120
73
SKL009 Skeletal Dysplasia, San Diego Type 11 9.120
74
GLS001 Gliosarcoma 59 6.449
75
ACT008 Actinic Keratosis 57 6.449
76
SCH063 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 57 6.449
77
GNT002 Giant Cell Glioblastoma 55 6.449
78
CRV040 Cervix Carcinoma 49 6.449
79
DYS018 Dysostosis 45 6.449
80
INV005 Inverted Follicular Keratosis 31 6.449
81
ISL061 Isolated Brachycephaly 23 6.449
82
ISL062 Isolated Plagiocephaly 21 6.449
83
CMP067 Camptodactyly-Tall Stature-Scoliosis-Hearing Loss Syndrome 11 6.449
84
P FGF008 Fgfr3-Related Isolated Coronal Synostosis 4 6.449
85
c FGF009 Fgfr3-Related Lacrimo-Auriculo-Dento-Digital Syndrome 4 6.449