Search results for "[genes] FGFR3"

97 hits were found for '[genes] FGFR3'

# Family MCID Name MIFTS Score
1
ACH004 Achondroplasia 65 22.766
2
HYP042 Hypochondroplasia 56 21.873
3
BLD087 Bladder Cancer, Somatic 58 20.942
4
P THN009 Thanatophoric Dysplasia, Type I 61 19.967
5
MNK003 Muenke Syndrome 54 19.967
6
LDD001 Ladd Syndrome 60 18.943
7
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 18.943
8
P CRN037 Craniosynostosis 57 17.859
9
CTS022 Catshl Syndrome 23 17.859
10
c THN010 Thanatophoric Dysplasia, Type Ii 45 16.706
11
P CLR023 Colorectal Cancer 95 15.467
12
c MLT019 Multiple Myeloma 77 15.467
13
CRZ001 Crouzon Syndrome 67 15.467
14
CRV047 Cervical Cancer, Somatic 61 15.467
15
TST021 Testicular Germ Cell Tumor 60 15.467
16
P MYL007 Myeloma 54 15.467
17
ACN002 Acanthosis Nigricans 53 15.467
18
CNN005 Connective Tissue Disease 49 15.467
19
OST015 Osteochondrodysplasia 46 15.467
20
BND014 Bone Development Disease 28 15.467
21
P STH001 Saethre-Chotzen Syndrome 65 14.119
22
P SYN001 Syndactyly 49 14.119
23
KRT009 Keratosis 43 14.119
24
DWR001 Dwarfism 42 14.119
25
SYN005 Synostosis 41 14.119
26
KRT036 Keratosis, Seborrheic, Somatic 38 14.119
27
SKL014 Skeletal Dysplasia 38 14.119
28
SDD003 Saddan 31 14.119
29
ATS008 Autosomal Dominant Disease 31 14.119
30
P PFF001 Pfeiffer Syndrome 71 12.629
31
P HYD006 Hydrocephalus 54 12.629
32
CHR003 Cherubism 51 12.629
33
PPL022 Papilloma 49 12.629
34
P SCL018 Scoliosis 44 12.629
35
P OST005 Osteogenesis Imperfecta 70 10.937
36
WLF002 Wolf-Hirschhorn Syndrome 52 10.937
37
ANT003 Antley-Bixler Syndrome 50 10.937
38
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 48 10.937
39
P OST028 Osteochondroma 40 10.937
40
PLY012 Polyhydramnios 39 10.937
41
EPD053 Epidermal Nevus, Somatic 39 10.937
42
SKL017 Skeletal Dysplasias 39 10.937
43
PRP036 Peripheral T-Cell Lymphoma 37 10.937
44
RDL002 Radioulnar Synostosis 35 10.937
45
PLG004 Plagiocephaly 33 10.937
46
LTM002 Luteoma 30 10.937
47
DRM003 Dermatosis Papulosa Nigra 25 10.937
48
FGF001 Fgfr-Related Craniosynostosis Syndromes 24 10.937
49
c FGF007 Fgfr3-Related Craniosynostosis 15 10.937
50
APR006 Apert Syndrome 63 8.930
51
c OST080 Osteogenesis Imperfecta, Type Ii 50 8.930
52
JCK001 Jackson-Weiss Syndrome 49 8.930
53
ACR011 Acromesomelic Dysplasia, Maroteaux Type 48 8.930
54
OST044 Osteoglophonic Dysplasia 47 8.930
55
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 47 8.930
56
MTP026 Metaphyseal Chondrodysplasia, Murk Jansen Type 46 8.930
57
LRW001 Leri-Weill Dyschondrosteosis 45 8.930
58
PLS009 Plasma Cell Neoplasm 45 8.930
59
PRK001 Porokeratosis 44 8.930
60
P EXP004 Exophthalmos 44 8.930
61
SYN031 Synovial Chondromatosis 38 8.930
62
CHR010 Chorioangioma 37 8.930
63
MNC006 Monoclonal Gammopathy of Uncertain Significance 37 8.930
64
MSN003 Mesenteric Vascular Occlusion 35 8.930
65
P CHR342 Chiari Malformation 35 8.930
66
CHN053 Chondromyxoid Fibroma 35 8.930
67
c CLL013 Cell Type Cancer 33 8.930
68
ACR016 Acromesomelic Dysplasia 32 8.930
69
ACR015 Acrocephalosyndactylia 31 8.930
70
HYP047 Hypertropia 31 8.930
71
PLS016 Plasma Cell Leukemia 30 8.930
72
ADN010 Adenosquamous Cell Lung Carcinoma 29 8.930
73
P ATL001 Atelosteogenesis 29 8.930
74
PGM003 Pigmentation Disease 26 8.930
75
SML011 Smoldering Myeloma 26 8.930
76
SPR018 Spermatocytoma 25 8.930
77
HMN011 Hemangioma of Intra-Abdominal Structure 23 8.930
78
NNN005 Non-Invasive Bladder Papillary Urothelial Neoplasm 20 8.930
79
URN011 Urinary Tract Papillary Transitional Cell Benign Neoplasm 19 8.930
80
BLD046 Bladder Papillary Transitional Cell Neoplasm 19 8.930
81
ISL062 Isolated Plagiocephaly 18 8.930
82
ALC001 Alcohol-Related Birth Defect 18 8.930
83
CMP065 Camptodactyly - Tall Stature - Scoliosis - Hearing Loss 11 8.930
84
SKL009 Skeletal Dysplasia, San Diego Type 9 8.930
85
SCH063 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 51 6.314
86
c CNG124 Congenital Rubella 47 6.314
87
c ALM001 Al Amyloidosis 45 6.314
88
GLS001 Gliosarcoma 45 6.314
89
ACT008 Actinic Keratosis 44 6.314
90
GNT002 Giant Cell Glioblastoma 43 6.314
91
WLL023 Woolly Hair Nevus 29 6.314
92
INV005 Inverted Follicular Keratosis 24 6.314
93
ISL061 Isolated Brachycephaly 22 6.314
94
TST010 Testicular Spermatocytic Seminoma 18 6.314
95
MCR074 Micromelic Bone Dysplasia with Cloverleaf Skull 13 6.314
96
P FGF008 Fgfr3-Related Isolated Coronal Synostosis 5 6.314
97
c FGF009 Fgfr3-Related Lacrimo-Auriculo-Dento-Digital Syndrome 4 6.314