Search results for "[genes] FGFR1"

65 hits were found for '[genes] FGFR1'

# Family MCID Name MIFTS Score
1
P PFF001 Pfeiffer Syndrome 72 22.267
2
OST044 Osteoglophonic Dysplasia 29 21.231
3
P KLL001 Kallmann Syndrome 61 17.763
4
HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 29 17.763
5
HRT030 Hartsfield Syndrome 25 17.763
6
P BRS047 Breast Cancer 100 16.445
7
P LNG032 Lung Cancer 95 16.445
8
HYP080 Hypogonadism 51 16.445
9
c TRG016 Trigonocephaly 1 24 16.445
10
P PRS040 Prostate Cancer 90 15.012
11
P PNC035 Pancreatic Cancer 88 15.012
12
P LYM118 Lymphoma 68 15.012
13
P CRN037 Craniosynostosis 65 15.012
14
CLF001 Cleft Lip 53 15.012
15
JCK001 Jackson-Weiss Syndrome 50 15.012
16
P ESN007 Eosinophilia 64 13.428
17
P HLP001 Holoprosencephaly 63 13.428
18
c SYS004 Systemic Mastocytosis 62 13.428
19
CRY002 Cryptorchidism 57 13.428
20
ANT003 Antley-Bixler Syndrome 51 13.428
21
SYN005 Synostosis 47 13.428
22
CRZ001 Crouzon Syndrome 70 11.629
23
P STH001 Saethre-Chotzen Syndrome 60 11.629
24
CLF027 Cleft Palate, Isolated 59 11.629
25
BNM001 Bone Marrow Cancer 58 11.629
26
KLN001 Klinefelter's Syndrome 58 11.629
27
HYP042 Hypochondroplasia 57 11.629
28
LNG039 Lung Squamous Cell Carcinoma 54 11.629
29
c LRG001 Large Cell Carcinoma 53 11.629
30
ANK001 Ankylosis 53 11.629
31
LYM040 Lymphoblastic Lymphoma 53 11.629
32
TTH002 Tooth Agenesis 52 11.629
33
RDL002 Radioulnar Synostosis 31 11.629
34
APR006 Apert Syndrome 67 9.495
35
P THN009 Thanatophoric Dysplasia, Type I 65 9.495
36
P PLC011 Pilocytic Astrocytoma 63 9.495
37
CHR103 Charge Syndrome 62 9.495
38
LDD001 Ladd Syndrome 60 9.495
39
MNK003 Muenke Syndrome 53 9.495
40
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 53 9.495
41
CHR563 Chronic Eosinophilic Leukemia 50 9.495
42
CSY001 C Syndrome 49 9.495
43
MSN003 Mesenteric Vascular Occlusion 48 9.495
44
ACR015 Acrocephalosyndactylia 44 9.495
45
BND014 Bone Development Disease 44 9.495
46
LNG026 Long Bone Adamantinoma 43 9.495
47
P LNG035 Lung Large Cell Carcinoma 42 9.495
48
c PFF007 Pfeiffer Syndrome Type 1 40 9.495
49
BRS062 Breast Secretory Carcinoma 39 9.495
50
PLG004 Plagiocephaly 38 9.495
51
P 8P1002 8p11 Myeloproliferative Syndrome 34 9.495
52
FGF001 Fgfr-Related Craniosynostosis Syndromes 32 9.495
53
CLC057 Cole-Carpenter Syndrome 32 9.495
54
GLS001 Gliosarcoma 59 6.714
55
GNT002 Giant Cell Glioblastoma 55 6.714
56
c PRM149 Primary Hypereosinophilic Syndrome 43 6.714
57
ENC010 Encephalocraniocutaneous Lipomatosis 32 6.714
58
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 32 6.714
59
ISL084 Isolated Trigonocephaly 19 6.714
60
FGF011 Fgfr1-Related Isolated Gonadotropin-Releasing Hormone Deficiency 15 6.714
61
MYL041 Myeloid Neoplasm Associated with Fgfr1 Rearrangement 14 6.714
62
HRT028 Hartsfield-Bixler-Demyer Syndrome 12 6.714
63
MYL054 Myeloid and Lymphoid Neoplasm with Fgfr1 Abnormalities 11 6.714
64
c FGF003 Fgfr1-Related Craniosynostosis 9 6.714
65
P TRG011 Trigonocephaly, Nonsyndromic 7 6.714