Search results for "[genes] FGFR1"

70 hits were found for '[genes] FGFR1'

# Family MCID Name MIFTS Score
1
P PFF001 Pfeiffer Syndrome 73 21.905
2
OST044 Osteoglophonic Dysplasia 49 20.886
3
HRT030 Hartsfield Syndrome 28 19.814
4
JCK001 Jackson-Weiss Syndrome 50 18.681
5
HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 31 17.474
6
ENC010 Encephalocraniocutaneous Lipomatosis 34 17.474
7
P BRS047 Breast Cancer 100 16.178
8
P KLL001 Kallmann Syndrome 61 16.178
9
c TRG016 Trigonocephaly 1 22 16.178
10
P PRS040 Prostate Cancer 89 14.768
11
P LNG032 Lung Cancer 92 14.768
12
P PNC035 Pancreatic Cancer 86 14.768
13
HYP080 Hypogonadism 54 14.768
14
LPM005 Lipomatosis 46 14.768
15
CRY002 Cryptorchidism 61 13.209
16
HYP042 Hypochondroplasia 55 13.209
17
P LYM118 Lymphoma 68 13.209
18
P CRN037 Craniosynostosis 66 13.209
19
P HLP001 Holoprosencephaly 62 13.209
20
ANT003 Antley-Bixler Syndrome 43 13.209
21
P ESN007 Eosinophilia 61 13.209
22
TTH002 Tooth Agenesis 54 13.209
23
CLF001 Cleft Lip 48 13.209
24
P CLD001 Cleidocranial Dysplasia 62 11.440
25
P STH001 Saethre-Chotzen Syndrome 61 11.440
26
CRZ001 Crouzon Syndrome 70 11.440
27
ACH004 Achondroplasia 64 11.440
28
CHR103 Charge Syndrome 64 11.440
29
CLF027 Cleft Palate, Isolated 56 11.440
30
c SYS004 Systemic Mastocytosis 60 11.440
31
RDL002 Radioulnar Synostosis 45 11.440
32
LNG039 Lung Squamous Cell Carcinoma 51 11.440
33
c BRS049 Breast Carcinoma in Situ 32 11.440
34
c LRG001 Large Cell Carcinoma 49 11.440
35
MGS001 Megaesophagus 35 11.440
36
SYN005 Synostosis 44 11.440
37
P NRB001 Neuroblastoma 70 9.340
38
APR006 Apert Syndrome 66 9.340
39
LDD001 Ladd Syndrome 60 9.340
40
MNK003 Muenke Syndrome 55 9.340
41
CSY001 C Syndrome 49 9.340
42
P PLC011 Pilocytic Astrocytoma 59 9.340
43
ADM013 Adamantinoma of Long Bones 57 9.340
44
CLC057 Cole-Carpenter Syndrome 33 9.340
45
LYM040 Lymphoblastic Lymphoma 51 9.340
46
BRS062 Breast Secretory Carcinoma 35 9.340
47
P SPL037 Split Hand Foot Malformation 35 9.340
48
PLG004 Plagiocephaly 40 9.340
49
SYN031 Synovial Chondromatosis 44 9.340
50
ACR015 Acrocephalosyndactylia 38 9.340
51
P LNG035 Lung Large Cell Carcinoma 41 9.340
52
CHR563 Chronic Eosinophilic Leukemia 46 9.340
53
P 8P1002 8p11 Myeloproliferative Syndrome 37 9.340
54
P OST028 Osteochondroma 45 9.340
55
BND014 Bone Development Disease 40 9.340
56
c PFF007 Pfeiffer Syndrome Type 1 35 9.340
57
FGF001 Fgfr-Related Craniosynostosis Syndromes 33 9.340
58
c FGF003 Fgfr1-Related Craniosynostosis 8 9.340
59
c LKM061 Leukemia, Acute Myeloid 71 6.605
60
P RNL100 Renal Hypodysplasia/aplasia 1 54 6.605
61
GLS001 Gliosarcoma 54 6.605
62
CHR375 Chromosome 8p11 Myeloproliferative Syndrome 16 6.605
63
GNT002 Giant Cell Glioblastoma 51 6.605
64
GND003 Gonadal Disease 41 6.605
65
c PRM149 Primary Hypereosinophilic Syndrome 39 6.605
66
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 36 6.605
67
ISL084 Isolated Trigonocephaly 17 6.605
68
FGF011 Fgfr1-Related Isolated Gonadotropin-Releasing Hormone Deficiency 9 6.605
69
MYL054 Myeloid and Lymphoid Neoplasm with Fgfr1 Abnormalities 8 6.605
70
P TRG011 Trigonocephaly, Nonsyndromic 6 6.605