Search results for "[genes] FGFR1"

72 hits were found for '[genes] FGFR1'

# Family MCID Name MIFTS Score
1
P PFF001 Pfeiffer Syndrome 73 21.805
2
OST044 Osteoglophonic Dysplasia 47 20.791
3
HRT030 Hartsfield Syndrome 30 19.724
4
JCK001 Jackson-Weiss Syndrome 49 18.596
5
P KLL001 Kallmann Syndrome 60 17.395
6
ENC010 Encephalocraniocutaneous Lipomatosis 34 17.395
7
HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 32 17.395
8
P BRS047 Breast Cancer 100 16.104
9
P LNG032 Lung Cancer 94 16.104
10
HYP080 Hypogonadism 54 16.104
11
c TRG016 Trigonocephaly 1 27 16.104
12
P PRS040 Prostate Cancer 89 14.701
13
P PNC035 Pancreatic Cancer 85 14.701
14
P LYM118 Lymphoma 70 14.701
15
P CRN037 Craniosynostosis 65 14.701
16
P ESN007 Eosinophilia 61 14.701
17
CLF001 Cleft Lip 49 14.701
18
LPM005 Lipomatosis 47 14.701
19
P HLP001 Holoprosencephaly 62 13.149
20
CRY002 Cryptorchidism 62 13.149
21
c SYS004 Systemic Mastocytosis 59 13.149
22
HYP042 Hypochondroplasia 57 13.149
23
LYM040 Lymphoblastic Lymphoma 54 13.149
24
SYN005 Synostosis 45 13.149
25
CRZ001 Crouzon Syndrome 70 11.388
26
APR006 Apert Syndrome 66 11.388
27
ACH004 Achondroplasia 66 11.388
28
CHR103 Charge Syndrome 64 11.388
29
P STH001 Saethre-Chotzen Syndrome 59 11.388
30
CLF027 Cleft Palate, Isolated 56 11.388
31
KLN001 Klinefelter's Syndrome 55 11.388
32
TTH002 Tooth Agenesis 55 11.388
33
LNG039 Lung Squamous Cell Carcinoma 52 11.388
34
BNM001 Bone Marrow Cancer 52 11.388
35
c LRG001 Large Cell Carcinoma 51 11.388
36
P HYP098 Hypereosinophilic Syndrome 51 11.388
37
CLF004 Cleft Lip/palate 46 11.388
38
RDL002 Radioulnar Synostosis 44 11.388
39
MGS001 Megaesophagus 37 11.388
40
c BRS049 Breast Carcinoma in Situ 33 11.388
41
P NRB001 Neuroblastoma 69 9.298
42
LDD001 Ladd Syndrome 60 9.298
43
P PLC011 Pilocytic Astrocytoma 58 9.298
44
MNK003 Muenke Syndrome 55 9.298
45
THR009 Thrombocytopenia-Absent Radius Syndrome 54 9.298
46
CSY001 C Syndrome 49 9.298
47
P OST028 Osteochondroma 48 9.298
48
CHR563 Chronic Eosinophilic Leukemia 47 9.298
49
PLG004 Plagiocephaly 42 9.298
50
BND014 Bone Development Disease 42 9.298
51
SYN031 Synovial Chondromatosis 41 9.298
52
P LNG035 Lung Large Cell Carcinoma 40 9.298
53
CHN004 Chondroblastoma 40 9.298
54
c ADL008 Adult Oligodendroglioma 37 9.298
55
c PFF007 Pfeiffer Syndrome Type 1 36 9.298
56
BRS062 Breast Secretory Carcinoma 36 9.298
57
P 8P1002 8p11 Myeloproliferative Syndrome 35 9.298
58
P SPL037 Split Hand Foot Malformation 32 9.298
59
FGF001 Fgfr-Related Craniosynostosis Syndromes 31 9.298
60
CLC057 Cole-Carpenter Syndrome 30 9.298
61
c FGF003 Fgfr1-Related Craniosynostosis 8 9.298
62
c LKM061 Leukemia, Acute Myeloid 71 6.575
63
GLS001 Gliosarcoma 55 6.575
64
GNT002 Giant Cell Glioblastoma 51 6.575
65
c PRM149 Primary Hypereosinophilic Syndrome 39 6.575
66
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 35 6.575
67
c PFF008 Pfeiffer Syndrome Type 1, 2 and 3 28 6.575
68
ISL084 Isolated Trigonocephaly 17 6.575
69
CHR375 Chromosome 8p11 Myeloproliferative Syndrome 16 6.575
70
FGF011 Fgfr1-Related Isolated Gonadotropin-Releasing Hormone Deficiency 9 6.575
71
MYL054 Myeloid and Lymphoid Neoplasm with Fgfr1 Abnormalities 8 6.575
72
P TRG011 Trigonocephaly, Nonsyndromic 7 6.575