Search results for "[genes] FGFR1"

73 hits were found for '[genes] FGFR1'

# Family MCID Name MIFTS Score
1
P PFF001 Pfeiffer Syndrome 71 22.846
2
P KLL001 Kallmann Syndrome 58 21.874
3
OST044 Osteoglophonic Dysplasia 47 20.856
4
HYP080 Hypogonadism 47 18.654
5
P BRS047 Breast Cancer 100 17.449
6
HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 32 17.449
7
HRT030 Hartsfield Syndrome 27 17.449
8
P LNG032 Lung Cancer 91 16.155
9
P CRN037 Craniosynostosis 57 16.155
10
SYN005 Synostosis 41 16.155
11
c TRG016 Trigonocephaly 1 20 16.155
12
P PRS040 Prostate Cancer 90 14.747
13
P PNC035 Pancreatic Cancer 78 14.747
14
P HLP001 Holoprosencephaly 62 14.747
15
JCK001 Jackson-Weiss Syndrome 49 14.747
16
P ESN007 Eosinophilia 48 14.747
17
CLF001 Cleft Lip 45 14.747
18
KLN001 Klinefelter's Syndrome 57 13.190
19
HYP042 Hypochondroplasia 56 13.190
20
c SYS004 Systemic Mastocytosis 56 13.190
21
CRY002 Cryptorchidism 52 13.190
22
ANT003 Antley-Bixler Syndrome 50 13.190
23
DYS018 Dysostosis 43 13.190
24
GND003 Gonadal Disease 28 13.190
25
BND014 Bone Development Disease 28 13.190
26
CRZ001 Crouzon Syndrome 67 11.423
27
P STH001 Saethre-Chotzen Syndrome 65 11.423
28
ACH004 Achondroplasia 65 11.423
29
CHR103 Charge Syndrome 62 11.423
30
CLF027 Cleft Palate, Isolated 52 11.423
31
LYM040 Lymphoblastic Lymphoma 48 11.423
32
TTH002 Tooth Agenesis 48 11.423
33
BNM001 Bone Marrow Cancer 47 11.423
34
c LRG001 Large Cell Carcinoma 43 11.423
35
c BRS049 Breast Carcinoma in Situ 41 11.423
36
LNG039 Lung Squamous Cell Carcinoma 41 11.423
37
RDL002 Radioulnar Synostosis 35 11.423
38
MGS001 Megaesophagus 33 11.423
39
ACR015 Acrocephalosyndactylia 31 11.423
40
CHR084 Chromosomal Disease 30 11.423
41
FGF011 Fgfr1-Related Isolated Gonadotropin-Releasing Hormone Deficiency 10 11.423
42
P NRB001 Neuroblastoma 73 9.327
43
APR006 Apert Syndrome 63 9.327
44
P THN009 Thanatophoric Dysplasia, Type I 61 9.327
45
LDD001 Ladd Syndrome 60 9.327
46
MNK003 Muenke Syndrome 54 9.327
47
P RNL100 Renal Hypodysplasia/aplasia 1 52 9.327
48
CSY001 C Syndrome 44 9.327
49
P OST028 Osteochondroma 40 9.327
50
SYN031 Synovial Chondromatosis 38 9.327
51
LNG026 Long Bone Adamantinoma 36 9.327
52
CHR563 Chronic Eosinophilic Leukemia 36 9.327
53
MSN003 Mesenteric Vascular Occlusion 35 9.327
54
P 8P1002 8p11 Myeloproliferative Syndrome 35 9.327
55
MLN057 Melanoma of Soft Parts 34 9.327
56
PLG004 Plagiocephaly 33 9.327
57
PHY002 Physical Disorder 33 9.327
58
c LNG035 Lung Large Cell Carcinoma 31 9.327
59
BRS062 Breast Secretory Carcinoma 30 9.327
60
c PFF007 Pfeiffer Syndrome Type 1 30 9.327
61
FGF001 Fgfr-Related Craniosynostosis Syndromes 24 9.327
62
ISL084 Isolated Trigonocephaly 19 9.327
63
HRT028 Hartsfield-Bixler-Demyer Syndrome 13 9.327
64
GLS001 Gliosarcoma 45 6.595
65
c SPN106 Spinocerebellar Ataxia 5 43 6.595
66
GNT002 Giant Cell Glioblastoma 43 6.595
67
P PLC011 Pilocytic Astrocytoma 42 6.595
68
c PRM149 Primary Hypereosinophilic Syndrome 29 6.595
69
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 28 6.595
70
MYL041 Myeloid Neoplasm Associated with Fgfr1 Rearrangement 12 6.595
71
MYL054 Myeloid and Lymphoid Neoplasm with Fgfr1 Abnormalities 10 6.595
72
c FGF003 Fgfr1-Related Craniosynostosis 8 6.595
73
P TRG011 Trigonocephaly, Nonsyndromic 7 6.595