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Search results for sox11

220 hits were found for sox11

# Family MCID Name MIFTS Score
1
c CFF014 Coffin-Siris Syndrome 9 32 42.484
2
P CFF008 Coffin-Siris Syndrome 1 64 36.375
3
MNT001 Mantle Cell Lymphoma 67 28.639
4
P LYM118 Lymphoma 67 16.206
5
BRK010 Burkitt Lymphoma 66 16.063
6
P MCR010 Microcephaly 60 14.897
7
CKT002 Cakut 47 12.884
8
CHR103 Charge Syndrome 66 11.659
9
P HYP077 Hypertrichosis 46 11.486
10
CLB010 Coloboma of Macula 53 11.077
11
CLL014 Cll/sll 45 10.271
12
P ANT088 Anterior Segment Dysgenesis 55 10.169
13
P CMP005 Campomelic Dysplasia 65 8.521
14
IMM141 Immunodeficiency 49 37 7.577
15
P NNS031 Non-Syndromic Intellectual Disability 32 7.577
16
c ATS203 Autosomal Dominant Non-Syndromic Intellectual Disability 45 7.577
17
SFT002 Soft Palate Cancer 31 7.577
18
TRC018 Tracheal Lymphoma 26 7.577
19
GLL013 Gallbladder Lymphoma 32 7.577
20
P BCL017 B-Cell Lymphoma 59 6.409
21
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 6.240
22
DFF005 Diffuse Large B-Cell Lymphoma 54 5.846
23
P LKM071 Leukemia, Chronic Lymphocytic 75 5.513
24
P LKM002 Leukemia 67 5.192
25
HRY003 Hairy Cell Leukemia 61 4.533
26
GLL048 Glial Tumor 52 4.524
27
GLM045 Glioma 63 4.524
28
P GST053 Gastric Cancer 83 4.217
29
LYM133 Lymphoma, Hodgkin, Classic 74 3.970
30
P FLL037 Follicular Lymphoma 74 3.865
31
P BRS047 Breast Cancer 98 3.799
32
MRG003 Marginal Zone B-Cell Lymphoma 52 3.756
33
LYM143 Lymphoma, Non-Hodgkin, Familial 75 3.719
34
P TRT010 Teratoma 51 3.700
35
P BCL004 B-Cell Non-Hodgkin Lymphoma 42 3.666
36
P HPT023 Hepatocellular Carcinoma 96 3.643
37
P NSP012 Nasopharyngeal Carcinoma 61 3.612
38
END057 Endometrial Cancer 72 3.557
39
SPN186 Spinal Cord Injury 61 3.443
40
MCR013 Microphthalmia 60 3.443
41
OVR094 Ovarian Epithelial Cancer 39 3.443
42
HGH043 High Grade Glioma 45 3.399
43
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 3.199
44
CLF027 Cleft Palate, Isolated 64 3.197
45
P PRS040 Prostate Cancer 95 3.067
46
SPL004 Splenic Marginal Zone Lymphoma 50 2.926
47
P BLD134 Bladder Cancer 79 2.852
48
P OVR042 Ovarian Cancer 88 2.852
49
LYM040 Lymphoblastic Lymphoma 53 2.852
50
c PRG020 Paragangliomas 3 39 2.807
51
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.775
52
P AVS003 Avascular Necrosis 41 2.738
53
OST003 Osteonecrosis 61 2.738
54
P ADN016 Adenocarcinoma 63 2.695
55
DBL002 Double Outlet Right Ventricle 57 2.695
56
OST012 Osteoarthritis 77 2.666
57
SRC027 Sarcoma, Synovial 58 2.610
58
P RHB003 Rhabdomyosarcoma 66 2.610
59
ANG020 Angiosarcoma 64 2.610
60
CRV035 Cervical Cancer 73 2.592
61
P FNG006 Feingold Syndrome 1 62 2.515
62
FRY006 Fryns Microphthalmia Syndrome 52 2.435
63
PTR032 Peters-Plus Syndrome 63 2.435
64
P CTR002 Cataract 60 2.435
65
GST033 Gestational Diabetes 61 2.435
66
CHR178 Chromosomal Triplication 34 2.435
67
P MDL005 Medulloblastoma 75 2.429
68
THY029 Thyroid Carcinoma 51 2.429
69
SVR004 Severe Combined Immunodeficiency 72 2.351
70
c THY109 Thyroid Cancer, Nonmedullary, 1 55 2.329
71
P PRR016 Pierre Robin Syndrome 50 2.262
72
MTR008 Mature B-Cell Neoplasm 35 2.262
73
P OPT006 Optic Nerve Disease 58 2.262
74
HLX001 Helix Syndrome 48 2.262
75
c HPT016 Hepatitis B 62 2.262
76
ISL075 Isolated Pierre Robin Sequence 29 2.262
77
PTT041 Pituitary Stalk Interruption Syndrome 54 2.218
78
PRS129 Prostatic Hyperplasia, Benign 49 2.169
79
SPP011 Suppression of Tumorigenicity 12 61 2.169
80
P SCH015 Schizophrenia 74 2.169
81
DCT002 Ductal Carcinoma in Situ 58 2.169
82
P HRP006 Herpes Simplex 65 2.169
83
c PRM299 Primary Cutaneous B-Cell Lymphoma 37 2.169
84
PRS021 Prostatic Adenoma 43 2.169
85
PRS045 Prostatic Hypertrophy 53 2.169
86
P INS002 in Situ Carcinoma 53 2.169
87
CYN002 Cyanosis, Transient Neonatal 43 2.069
88
FBR019 Fibromatosis 42 1.977
89
GLB002 Glioblastoma 67 1.962
90
THY128 Thyroid Tumor 35 1.846
91
c PCH010 Pachyonychia Congenita 3 43 1.846
92
P EPL164 Epilepsy 68 1.846
93
FCL014 Focal Epilepsy 53 1.846
94
P TMP001 Temporal Lobe Epilepsy 49 1.846
95
P DYS021 Dysautonomia 38 1.846
96
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.717
97
P LKM062 Leukemia, Acute Lymphoblastic 69 1.717
98
TRT001 Teratocarcinoma 42 1.571
99
EMB004 Embryonal Carcinoma 56 1.571
100
ORL011 Oral Cancer 60 1.541
101
BRN032 Brain Glioma 45 1.442
102
c LKM061 Leukemia, Acute Myeloid 83 1.398
103
P MYL006 Myeloid Leukemia 61 1.398
104
PRS002 Prostate Lymphoma 25 1.398
105
FSC004 Fasciitis 49 1.398
106
CMP001 Composite Lymphoma 36 1.335
107
NCL006 Nicolaides-Baraitser Syndrome 46 1.218
108
GRM010 Germ Cells Tumors 33 1.218
109
PPL052 Papillomatosis, Confluent and Reticulated 34 1.090
110
DWR001 Dwarfism 44 1.090
111
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 41 0.944
112
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.944
113
AGN016 Aging 54 0.944
114
c BRN108 Branchiootic Syndrome 1 62 0.944
115
ACH004 Achondroplasia 66 0.944
116
SPL018 Splenomegaly 49 0.944
117
P HYP265 Hypotonia 42 0.944
118
TCL012 T-Cell/histiocyte Rich Large B Cell Lymphoma 31 0.944
119
P PRC031 Preeclampsia/eclampsia 1 43 0.816
120
c PRC016 Pre-Eclampsia 65 0.816
121
SYN106 Syndromic Craniosynostosis 32 0.771
122
CHR101 Char Syndrome 53 0.771
123
CHN065 Choanal Atresia, Posterior 48 0.771
124
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.771
125
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.771
126
LMB069 Lamb-Shaffer Syndrome 34 0.771
127
BRJ001 Borjeson-Forssman-Lehmann Syndrome 50 0.771
128
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.771
129
c GLC092 Glaucoma, Primary Open Angle 62 0.771
130
P ANR048 Aniridia 1 64 0.771
131
c CFF015 Coffin-Siris Syndrome 10 22 0.771
132
P OPN001 Open-Angle Glaucoma 55 0.771
133
CRC021 Carcinosarcoma 64 0.771
134
LMB050 Limbal Stem Cell Deficiency 50 0.771
135
P SKN015 Skin Carcinoma 71 0.771
136
DSS008 Disease of Mental Health 74 0.771
137
MRK001 Merkel Cell Carcinoma 64 0.771
138
PLC002 Plica Syndrome 35 0.771
139
P CRN037 Craniosynostosis 68 0.771
140
UTR024 Uterine Carcinosarcoma 59 0.771
141
P EYD002 Eye Disease 57 0.771
142
SYN007 Synovitis 55 0.771
143
ISL001 Islet Cell Tumor 56 0.771
144
NRN004 Neuroendocrine Tumor 59 0.771
145
P PNC035 Pancreatic Cancer 86 0.602
146
P ATS364 Autism 69 0.545
147
CLF004 Cleft Lip/palate 57 0.545
148
SPS057 Spasticity 42 0.545
149
P RHM011 Rheumatoid Arthritis 82 0.545
150
P FML011 Familial Adenomatous Polyposis 71 0.545
151
LYM012 Lymphoplasmacytic Lymphoma 50 0.545
152
c ATS007 Autism Spectrum Disorder 72 0.545
153
CLT003 Colitis 63 0.545
154
c FNC043 Fanconi Anemia, Complementation Group E 62 0.545
155
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.545
156
P FNC044 Fanconi Anemia, Complementation Group C 56 0.545
157
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.545
158
NRL016 Neural Tube Defects 81 0.545
159
c CFF011 Coffin-Siris Syndrome 6 35 0.545
160
DWN001 Down Syndrome 70 0.545
161
MYL069 Myeloma, Multiple 77 0.545
162
P RTN024 Retinoblastoma 73 0.545
163
c SPS147 Spastic Paraplegia 4, Autosomal Dominant 55 0.545
164
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 0.545
165
c SML038 Small Cell Cancer of the Lung 69 0.545
166
FLT011 Felty Syndrome 52 0.545
167
GST019 Gastrointestinal Stromal Tumor 78 0.545
168
MNN043 Meningioma, Familial 79 0.545
169
P SYN057 Syndromic Intellectual Disability 38 0.545
170
OVR105 Ovarian Serous Carcinoma 37 0.545
171
ADN011 Adenoid Cystic Carcinoma 68 0.545
172
P HYP730 Hypogonadotropic Hypogonadism 53 0.545
173
CST005 Castleman Disease 56 0.545
174
P NRB001 Neuroblastoma 66 0.545
175
SCR011 Scrapie 39 0.545
176
PDT014 Pediatric Ependymoma 28 0.545
177
CLF001 Cleft Lip 53 0.545
178
IRD001 Iridocyclitis 53 0.545
179
EXP004 Exophthalmos 51 0.545
180
P ATR005 Atrophic Gastritis 50 0.545
181
ULC004 Ulcerative Colitis 74 0.545
182
CLL010 Cellular Ependymoma 57 0.545
183
DFF029 Diffuse Large B-Cell Lymphoma of the Central Nervous System 29 0.545
184
CLF056 Cleft Lip with or Without Cleft Palate 42 0.545
185
HST010 Histiocytosis 49 0.545
186
P GST044 Gastritis 55 0.545
187
P SYP003 Syphilis 59 0.545
188
P ART023 Arthropathy 61 0.545
189
CLR030 Clear Cell Renal Cell Carcinoma 54 0.545
190
SCR001 Secretory Meningioma 40 0.545
191
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.545
192
PRP016 Paraplegia 52 0.545
193
P ART022 Arthritis 71 0.545
194
P BNG030 Benign Ependymoma 51 0.545
195
P LNG064 Lung Cancer Susceptibility 3 70 0.545
196
PRL017 Prolymphocytic Leukemia 47 0.545
197
HYP084 Hypopyon 38 0.545
198
P UVT001 Uveitis 57 0.545
199
P MLN008 Melanoma 76 0.545
200
c HRD010 Hereditary Spastic Paraplegia 66 0.545
201
PLY010 Polyclonal Hypergammaglobulinemia 35 0.545
202
PRG009 Progressive Multifocal Leukoencephalopathy 58 0.545
203
P PRN023 Prion Disease 60 0.545
204
TST018 Testicular Yolk Sac Tumor 39 0.545
205
PTT001 Pituitary Hypoplasia 34 0.545
206
ACN001 Acinar Cell Carcinoma 45 0.545
207
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.545
208
SPN021 Spinal Meningioma 50 0.545
209
P END039 Endodermal Sinus Tumor 41 0.545
210
HYP080 Hypogonadism 50 0.545
213
P ENC018 Encephalopathy 62 0.545
214
c SPS091 Spastic Paraplegia 4 27 0.545
215
P BCL005 B Cell Prolymphocytic Leukemia 39 0.545
216
PNS014 Penis Agenesis 36 0.545
217
LYM019 Lymphosarcoma 46 0.545
218
P RTT002 Rett Syndrome 79 0.401
219
c WLM018 Wilms Tumor 5 53 0.401
220
c NRB010 Neuroblastoma 1 59 0.401
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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