Search results for "[genes] FGFR1"

74 hits were found for '[genes] FGFR1'

# Family MCID Name MIFTS Score
1
P PFF001 Pfeiffer Syndrome 73 21.768
2
OST044 Osteoglophonic Dysplasia 47 20.755
3
HRT030 Hartsfield Syndrome 30 19.690
4
JCK001 Jackson-Weiss Syndrome 49 18.564
5
P BRS047 Breast Cancer 100 17.365
6
P LNG032 Lung Cancer 95 17.365
7
P KLL001 Kallmann Syndrome 61 17.365
8
HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 32 17.365
9
P PRS040 Prostate Cancer 90 16.077
10
P HYP098 Hypereosinophilic Syndrome 63 16.077
11
HYP080 Hypogonadism 53 16.077
12
ENC010 Encephalocraniocutaneous Lipomatosis 35 16.077
13
c TRG016 Trigonocephaly 1 26 16.077
14
P PNC035 Pancreatic Cancer 87 14.676
15
P CRN037 Craniosynostosis 66 14.676
16
CRY002 Cryptorchidism 60 14.676
17
c SYS004 Systemic Mastocytosis 60 14.676
18
HYP042 Hypochondroplasia 57 14.676
19
CLF001 Cleft Lip 50 14.676
20
LPM005 Lipomatosis 47 14.676
21
SYN005 Synostosis 46 14.676
22
CRZ001 Crouzon Syndrome 70 13.126
23
APR006 Apert Syndrome 67 13.126
24
ACH004 Achondroplasia 66 13.126
25
P AST007 Astrocytoma 65 13.126
26
CHR103 Charge Syndrome 62 13.126
27
MNK003 Muenke Syndrome 60 13.126
28
P STH001 Saethre-Chotzen Syndrome 60 13.126
29
CLF027 Cleft Palate, Isolated 55 13.126
30
TTH002 Tooth Agenesis 54 13.126
31
LNG039 Lung Squamous Cell Carcinoma 54 13.126
32
LYM040 Lymphoblastic Lymphoma 53 13.126
33
c BRS049 Breast Carcinoma in Situ 51 13.126
34
c LRG001 Large Cell Carcinoma 51 13.126
35
BNM001 Bone Marrow Cancer 51 13.126
36
ANT003 Antley-Bixler Syndrome 48 13.126
37
ATY042 Atypical Chronic Myeloid Leukemia 48 13.126
38
RDL002 Radioulnar Synostosis 44 13.126
39
c PFF007 Pfeiffer Syndrome Type 1 36 13.126
40
MGS001 Megaesophagus 34 13.126
41
P NRB001 Neuroblastoma 70 11.368
42
P PLC011 Pilocytic Astrocytoma 60 11.368
43
LDD001 Ladd Syndrome 59 11.368
44
MYL031 Myeloproliferative Neoplasm 58 11.368
45
GNT002 Giant Cell Glioblastoma 51 11.368
46
CSY001 C Syndrome 50 11.368
47
P OST028 Osteochondroma 47 11.368
48
CHR563 Chronic Eosinophilic Leukemia 46 11.368
49
CLF004 Cleft Lip/palate 46 11.368
50
PLG004 Plagiocephaly 43 11.368
51
SYN031 Synovial Chondromatosis 42 11.368
52
CHN004 Chondroblastoma 40 11.368
53
BND014 Bone Development Disease 40 11.368
54
c PRM149 Primary Hypereosinophilic Syndrome 38 11.368
55
P LNG035 Lung Large Cell Carcinoma 38 11.368
56
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 36 11.368
57
P 8P1002 8p11 Myeloproliferative Syndrome 36 11.368
58
c ADL008 Adult Oligodendroglioma 35 11.368
59
BRS062 Breast Secretory Carcinoma 34 11.368
60
P SPL037 Split Hand Foot Malformation 33 11.368
61
CLC057 Cole-Carpenter Syndrome 33 11.368
62
FGF001 Fgfr-Related Craniosynostosis Syndromes 32 11.368
63
ISL084 Isolated Trigonocephaly 17 11.368
64
CHR375 Chromosome 8p11 Myeloproliferative Syndrome 16 11.368
65
FGF011 Fgfr1-Related Isolated Gonadotropin-Releasing Hormone Deficiency 9 11.368
66
MYL054 Myeloid and Lymphoid Neoplasm with Fgfr1 Abnormalities 8 11.368
67
c FGF003 Fgfr1-Related Craniosynostosis 7 11.368
68
P TRG011 Trigonocephaly, Nonsyndromic 7 11.368
69
c LKM061 Leukemia, Acute Myeloid 73 9.282
70
GLS001 Gliosarcoma 55 9.282
71
c MYS055 Myasthenic Syndrome, Congenital, 6, Presynaptic 35 9.282
72
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 29 9.282
73
MYL059 Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 29 9.282
74
c PFF008 Pfeiffer Syndrome Type 1, 2 and 3 28 9.282