Search results for "[genes] FGFR3"

85 hits were found for '[genes] FGFR3'

# Family MCID Name MIFTS Score
1
ACH004 Achondroplasia 65 22.340
2
HYP042 Hypochondroplasia 57 21.389
3
MNK003 Muenke Syndrome 55 20.394
4
P THN009 Thanatophoric Dysplasia, Type I 62 19.347
5
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 34 19.347
6
LDD001 Ladd Syndrome 61 18.241
7
BLD087 Bladder Cancer, Somatic 51 18.241
8
SDD003 Saddan 29 18.241
9
CTS022 Catshl Syndrome 21 18.241
10
P CLR023 Colorectal Cancer 91 17.063
11
c THN010 Thanatophoric Dysplasia, Type Ii 45 17.063
12
c MLT019 Multiple Myeloma 71 15.797
13
CRZ001 Crouzon Syndrome 66 15.797
14
P CRN037 Craniosynostosis 61 15.797
15
CRV047 Cervical Cancer, Somatic 60 15.797
16
ACN002 Acanthosis Nigricans 50 15.797
17
P MYL007 Myeloma 50 15.797
18
P STH001 Saethre-Chotzen Syndrome 62 14.421
19
URN008 Urinary Bladder Cancer 60 14.421
20
TST021 Testicular Germ Cell Tumor 57 14.421
21
P SYN001 Syndactyly 48 14.421
22
KRT009 Keratosis 44 14.421
23
KRT036 Keratosis, Seborrheic, Somatic 41 14.421
24
SKL014 Skeletal Dysplasia 40 14.421
25
DWR001 Dwarfism 36 14.421
26
CHR003 Cherubism 53 12.898
27
PPL022 Papilloma 52 12.898
28
EMB004 Embryonal Carcinoma 50 12.898
29
TRN018 Transitional Cell Carcinoma 50 12.898
30
SYN005 Synostosis 42 12.898
31
P SCL018 Scoliosis 42 12.898
32
P PFF001 Pfeiffer Syndrome 69 11.170
33
WLF002 Wolf-Hirschhorn Syndrome 51 11.170
34
OST015 Osteochondrodysplasia 48 11.170
35
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 43 11.170
36
EPD053 Epidermal Nevus, Somatic 42 11.170
37
PLG004 Plagiocephaly 37 11.170
38
SKL017 Skeletal Dysplasias 37 11.170
39
PLY012 Polyhydramnios 36 11.170
40
ATS008 Autosomal Dominant Disease 34 11.170
41
PRP036 Peripheral T-Cell Lymphoma 33 11.170
42
FGF001 Fgfr-Related Craniosynostosis Syndromes 29 11.170
43
DRM003 Dermatosis Papulosa Nigra 28 11.170
44
c FGF007 Fgfr3-Related Craniosynostosis 11 11.170
45
APR006 Apert Syndrome 63 9.120
46
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 54 9.120
47
SDC002 Sed Congenita 53 9.120
48
ACR011 Acromesomelic Dysplasia, Maroteaux Type 52 9.120
49
JCK001 Jackson-Weiss Syndrome 51 9.120
50
c OST080 Osteogenesis Imperfecta, Type Ii 49 9.120
51
P KBK002 Kabuki Syndrome 1 47 9.120
52
MTP026 Metaphyseal Chondrodysplasia, Murk Jansen Type 46 9.120
53
PLS016 Plasma Cell Leukemia 45 9.120
54
PLS009 Plasma Cell Neoplasm 43 9.120
55
MSN003 Mesenteric Vascular Occlusion 40 9.120
56
ACT093 Actinic Cheilitis 38 9.120
57
ADN010 Adenosquamous Cell Lung Carcinoma 37 9.120
58
P OST028 Osteochondroma 36 9.120
59
ACR015 Acrocephalosyndactylia 35 9.120
60
P ATL001 Atelosteogenesis 34 9.120
61
BND014 Bone Development Disease 33 9.120
62
CHR010 Chorioangioma 33 9.120
63
ACR016 Acromesomelic Dysplasia 33 9.120
64
HYP047 Hypertropia 30 9.120
65
P CHR342 Chiari Malformation 29 9.120
66
SML011 Smoldering Myeloma 24 9.120
67
PGM003 Pigmentation Disease 24 9.120
68
HMN011 Hemangioma of Intra-Abdominal Structure 21 9.120
69
ALC001 Alcohol-Related Birth Defect 20 9.120
70
BLD046 Bladder Papillary Transitional Cell Neoplasm 19 9.120
71
NNN005 Non-Invasive Bladder Papillary Urothelial Neoplasm 18 9.120
72
URN011 Urinary Tract Papillary Transitional Cell Benign Neoplasm 18 9.120
73
SKL009 Skeletal Dysplasia, San Diego Type 9 9.120
74
SCH063 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 55 6.449
75
ACT008 Actinic Keratosis 47 6.449
76
GLS001 Gliosarcoma 46 6.449
77
CRV040 Cervix Carcinoma 43 6.449
78
GNT002 Giant Cell Glioblastoma 42 6.449
79
DYS018 Dysostosis 38 6.449
80
INV005 Inverted Follicular Keratosis 27 6.449
81
ISL061 Isolated Brachycephaly 22 6.449
82
ISL062 Isolated Plagiocephaly 20 6.449
83
CMP067 Camptodactyly-Tall Stature-Scoliosis-Hearing Loss Syndrome 10 6.449
84
P FGF008 Fgfr3-Related Isolated Coronal Synostosis 3 6.449
85
c FGF009 Fgfr3-Related Lacrimo-Auriculo-Dento-Digital Syndrome 3 6.449