Search results for "[genes] FGFR1"

65 hits were found for '[genes] FGFR1'

# Family MCID Name MIFTS Score
1
P PFF001 Pfeiffer Syndrome 69 22.267
2
OST044 Osteoglophonic Dysplasia 34 21.231
3
P KLL001 Kallmann Syndrome 58 17.763
4
HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 29 17.763
5
HRT030 Hartsfield Syndrome 26 17.763
6
P BRS047 Breast Cancer 100 16.445
7
P LNG032 Lung Cancer 91 16.445
8
HYP080 Hypogonadism 45 16.445
9
c TRG016 Trigonocephaly 1 28 16.445
10
P PRS040 Prostate Cancer 87 15.012
11
P PNC035 Pancreatic Cancer 82 15.012
12
P CRN037 Craniosynostosis 61 15.012
13
P LYM118 Lymphoma 57 15.012
14
JCK001 Jackson-Weiss Syndrome 51 15.012
15
CLF001 Cleft Lip 44 15.012
16
P HLP001 Holoprosencephaly 63 13.428
17
c SYS004 Systemic Mastocytosis 53 13.428
18
CRY002 Cryptorchidism 53 13.428
19
P ESN007 Eosinophilia 52 13.428
20
ANT003 Antley-Bixler Syndrome 51 13.428
21
SYN005 Synostosis 42 13.428
22
CRZ001 Crouzon Syndrome 66 11.629
23
P STH001 Saethre-Chotzen Syndrome 62 11.629
24
HYP042 Hypochondroplasia 57 11.629
25
CLF027 Cleft Palate, Isolated 53 11.629
26
TTH002 Tooth Agenesis 51 11.629
27
BNM001 Bone Marrow Cancer 46 11.629
28
KLN001 Klinefelter's Syndrome 46 11.629
29
LNG039 Lung Squamous Cell Carcinoma 45 11.629
30
LYM040 Lymphoblastic Lymphoma 44 11.629
31
c LRG001 Large Cell Carcinoma 43 11.629
32
ANK001 Ankylosis 42 11.629
33
RDL002 Radioulnar Synostosis 30 11.629
34
APR006 Apert Syndrome 63 9.495
35
P THN009 Thanatophoric Dysplasia, Type I 62 9.495
36
LDD001 Ladd Syndrome 61 9.495
37
CHR103 Charge Syndrome 59 9.495
38
MNK003 Muenke Syndrome 55 9.495
39
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 54 9.495
40
P PLC011 Pilocytic Astrocytoma 52 9.495
41
MSN003 Mesenteric Vascular Occlusion 40 9.495
42
LNG026 Long Bone Adamantinoma 39 9.495
43
CSY001 C Syndrome 39 9.495
44
CHR563 Chronic Eosinophilic Leukemia 39 9.495
45
PLG004 Plagiocephaly 37 9.495
46
ACR015 Acrocephalosyndactylia 35 9.495
47
P LNG035 Lung Large Cell Carcinoma 35 9.495
48
c PFF007 Pfeiffer Syndrome Type 1 34 9.495
49
BND014 Bone Development Disease 33 9.495
50
CLC057 Cole-Carpenter Syndrome 32 9.495
51
BRS062 Breast Secretory Carcinoma 30 9.495
52
P 8P1002 8p11 Myeloproliferative Syndrome 30 9.495
53
FGF001 Fgfr-Related Craniosynostosis Syndromes 29 9.495
54
GLS001 Gliosarcoma 46 6.714
55
GNT002 Giant Cell Glioblastoma 42 6.714
56
c PRM149 Primary Hypereosinophilic Syndrome 33 6.714
57
ENC010 Encephalocraniocutaneous Lipomatosis 32 6.714
58
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 29 6.714
59
ISL084 Isolated Trigonocephaly 18 6.714
60
MYL041 Myeloid Neoplasm Associated with Fgfr1 Rearrangement 13 6.714
61
HRT028 Hartsfield-Bixler-Demyer Syndrome 11 6.714
62
FGF011 Fgfr1-Related Isolated Gonadotropin-Releasing Hormone Deficiency 10 6.714
63
MYL054 Myeloid and Lymphoid Neoplasm with Fgfr1 Abnormalities 9 6.714
64
c FGF003 Fgfr1-Related Craniosynostosis 7 6.714
65
P TRG011 Trigonocephaly, Nonsyndromic 6 6.714