Search results for "[genes] FGFR2"

50 hits were found for '[genes] FGFR2'

# Family MCID Name MIFTS Score
1
CRZ001 Crouzon Syndrome 68 36.581
2
JCK001 Jackson-Weiss Syndrome 52 36.581
3
APR006 Apert Syndrome 66 31.680
4
P PFF001 Pfeiffer Syndrome 74 30.917
5
BRS002 Beare-Stevenson Cutis Gyrata Syndrome 45 29.330
6
P STH001 Saethre-Chotzen Syndrome 67 23.948
7
LDD001 Ladd Syndrome 56 21.861
8
P CRN037 Craniosynostosis 60 19.553
9
ACH004 Achondroplasia 68 16.934
10
ANT003 Antley-Bixler Syndrome 57 16.934
11
BNT003 Bent Bone Dysplasia Syndrome 17 15.458
12
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 13 15.458
13
END057 Endometrial Cancer 71 13.826
14
HYP042 Hypochondroplasia 61 13.826
15
ACN002 Acanthosis Nigricans 55 13.826
16
P EXP004 Exophthalmos 47 13.826
17
SYN005 Synostosis 43 13.826
18
P BRS047 Breast Cancer 90 11.974
19
c PFF007 Pfeiffer Syndrome Type 1 35 11.974
20
SCP007 Scaphocephaly, Maxillary Retrusion, and Mental Retardation 10 11.974
21
P CLR023 Colorectal Cancer 96 9.777
22
P THN009 Thanatophoric Dysplasia, Type I 62 9.777
23
P STM004 Stomach Cancer 59 9.777
24
MNK003 Muenke Syndrome 56 9.777
25
WLL006 Wells Syndrome 54 9.777
26
OST044 Osteoglophonic Dysplasia 51 9.777
27
GLM004 Gliomatosis Cerebri 50 9.777
28
P SYR001 Syringomyelia 49 9.777
29
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 46 9.777
30
GST060 Gastric Cancer, Somatic 45 9.777
31
RDL002 Radioulnar Synostosis 40 9.777
32
PLG004 Plagiocephaly 39 9.777
33
ACN010 Acanthoma 39 9.777
34
HYW001 Hay-Wells Syndrome 35 9.777
35
CYT014 Cytochrome P450 Oxidoreductase Deficiency 35 9.777
36
ACR015 Acrocephalosyndactylia 32 9.777
37
P CLR001 Clear Cell Acanthoma 31 9.777
38
FGF001 Fgfr-Related Craniosynostosis Syndromes 28 9.777
39
CTS039 Cutis Gyrata - Acanthosis Nigricans - Craniosynostosis 19 9.777
40
HMR015 Humeroradial Synostosis 13 9.777
41
FML273 Familial Scaphocephaly Syndrome, Mcgillivray Type 12 9.777
42
FGF010 Fgfr2-Related Bent Bone Dysplasia 6 9.777
43
c SPN106 Spinocerebellar Ataxia 5 44 6.913
44
CRD019 Cardiocranial Syndrome 26 6.913
45
c PFF009 Pfeiffer Syndrome Type 3 20 6.913
46
c FGF004 Fgfr2-Related Craniosynostosis 9 6.913
47
c PFF008 Pfeiffer Syndrome Type 1, 2 and 3 7 6.913
48
c STH004 Saethre-Chotzen Syndrome, Fgfr2-Related 5 6.913
49
c FGF005 Fgfr2-Related Isolated Coronal Synostosis 3 6.913
50
P FGF006 Fgfr2-Related Lacrimo-Auriculo-Dento-Digital Syndrome 3 6.913