Search results for "FGFR1"

87 hits were found for 'FGFR1'

# Family MCID Name MIFTS Score
1
MYL041 Myeloid Neoplasm Associated with Fgfr1 Rearrangement 17 10.362
2
c 8P1002 8p11 Myeloproliferative Syndrome 38 10.259
3
OST044 Osteoglophonic Dysplasia 56 7.754
4
c PFF001 Pfeiffer Syndrome 55 5.940
5
JCK001 Jackson-Weiss Syndrome 58 4.769
6
P KLL001 Kallmann Syndrome 57 4.386
7
HRT030 Hartsfield Syndrome 26 4.178
8
c CRN037 Craniosynostosis 70 4.155
9
HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 14 4.155
10
P TRG016 Trigonocephaly 1 27 4.130
11
INF030 Infectious Mononucleosis 84 3.402
12
CLF001 Cleft Lip 60 3.402
13
c SYN005 Synostosis 54 3.402
14
CRZ001 Crouzon Syndrome 78 3.372
15
HYP042 Hypochondroplasia 69 3.372
16
ANT003 Antley-Bixler Syndrome 56 3.372
17
P PNC035 Pancreatic Cancer 93 2.921
18
SPT014 Septo-Optic Dysplasia 69 2.921
19
HYP444 Hypogonadotropic Hypogonadism 9 with or Without Anosmia 54 2.921
20
c KLL004 Kallmann Syndrome 2 14 2.921
21
SLV021 Salivary Gland Tumor 44 2.425
22
c KLL003 Kallmann Syndrome 1 33 2.425
23
ACH004 Achondroplasia 78 2.385
24
P CLR023 Colorectal Cancer 77 2.385
25
P STH001 Saethre-Chotzen Syndrome 76 2.385
26
ACR015 Acrocephalosyndactylia 65 2.385
27
MNK003 Muenke Syndrome 63 2.385
28
GLM004 Gliomatosis Cerebri 59 2.385
29
c OST028 Osteochondroma 54 2.385
30
LBL001 Lobular Neoplasia 50 2.385
31
PLG004 Plagiocephaly 46 2.385
32
RDL002 Radioulnar Synostosis 44 2.385
33
P PFF007 Pfeiffer Syndrome Type 1 39 2.385
34
FGF001 Fgfr-Related Craniosynostosis Syndromes 34 2.385
35
P PLC011 Pilocytic Astrocytoma 57 1.739
36
GLS001 Gliosarcoma 61 1.686
37
GNT002 Giant Cell Glioblastoma 55 1.686
38
HYP523 Hypogonadotropic Hypogonadism 14 with or Without Anosmia 48 1.686
39
TTH016 Tooth Agenesis, Selective, 1, with or Without Orofacial Cleft 40 1.686
40
c FGF003 Fgfr1-Related Craniosynostosis 10 1.686
41
c TRG011 Trigonocephaly, Nonsyndromic 7 1.686
42
FGF011 Fgfr1-Related Isolated Gonadotropin-Releasing Hormone Deficiency 5 1.686
43
P LNG032 Lung Cancer 79 0.167
44
P LKM002 Leukemia 77 0.167
45
c MYL006 Myeloid Leukemia 75 0.155
46
PRS047 Prostatitis 60 0.155
47
P ACT019 Acute Myeloid Leukemia 93 0.126
48
P BRS047 Breast Cancer 86 0.126
49
P ESN007 Eosinophilia 63 0.126
50
P PRS040 Prostate Cancer 98 0.109
51
P HYP080 Hypogonadism 60 0.109
52
HYP064 Hypogonadotropism 46 0.109
53
c CHR065 Chronic Myeloid Leukemia 73 0.089
54
LYM040 Lymphoblastic Lymphoma 54 0.089
55
ORL015 Oral Squamous Cell Carcinoma 38 0.089
56
P OBS005 Obesity 91 0.063
57
P SCH015 Schizophrenia 82 0.063
58
BRK003 Burkitt's Lymphoma 77 0.063
59
P BPL003 Bipolar Disorder 77 0.063
60
P MST009 Mastocytosis 75 0.063
61
P AST007 Astrocytoma 74 0.063
62
c AMY001 Amyotrophic Lateral Sclerosis 67 0.063
63
P MLN008 Melanoma 65 0.063
64
ABT001 Abetalipoproteinemia 65 0.063
65
c HLP001 Holoprosencephaly 64 0.063
66
P RNL014 Renal Cell Carcinoma 64 0.063
67
CRY002 Cryptorchidism 63 0.063
68
c AMY077 Amyotrophic Lateral Sclerosis Type 18 60 0.063
69
c SYS004 Systemic Mastocytosis 59 0.063
70
RHB003 Rhabdomyosarcoma 59 0.063
71
c ACT073 Acute Leukemia 57 0.063
72
c LYM026 Lymphoblastic Leukemia 57 0.063
73
P AMY074 Amyotrophic Lateral Sclerosis Type 14 56 0.063
74
BNM001 Bone Marrow Cancer 54 0.063
75
RTN023 Retinitis 54 0.063
76
END072 Endotheliitis 51 0.063
77
MMR004 Memory Impairment 51 0.063
78
HYP017 Hypophosphatemia 49 0.063
79
NRN002 Neuronitis 44 0.063
80
TTH002 Tooth Agenesis 43 0.063
81
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.063
82
PPL039 Papillary Glioneuronal Tumor 41 0.063
83
SPL040 Split Hand 40 0.063
84
GST053 Gastric Cancer 38 0.063
85
LNG039 Lung Squamous Cell Carcinoma 37 0.063
86
c SPL037 Split Hand Foot Malformation 35 0.063
87
SYN053 Syndromic Diarrhea 34 0.063