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Search results for foxg1

293 hits were found for foxg1

# Family MCID Name MIFTS Score
1
FXG001 Foxg1 Syndrome 27 63.769
2
RTT008 Rett Syndrome, Congenital Variant 33 56.130
3
P RTT002 Rett Syndrome 79 56.076
4
P STR020 Strabismus 56 21.621
5
P MCR010 Microcephaly 59 20.148
6
P OPT006 Optic Nerve Disease 57 17.026
7
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 12.885
8
WST001 West Syndrome 64 12.039
9
P MDL005 Medulloblastoma 75 11.924
10
DSS008 Disease of Mental Health 74 11.836
11
P ATS364 Autism 72 11.681
12
P HLP001 Holoprosencephaly 69 10.960
13
c AMY091 Amyotrophic Lateral Sclerosis 1 88 9.569
14
CHR073 Choreatic Disease 53 8.484
15
LNN001 Lennox-Gastaut Syndrome 61 8.464
16
MCP054 Mecp2 Disorders 16 8.157
17
14Q001 14q12 Microdeletion Syndrome 16 8.154
18
14Q003 14q11.2 Microduplication Syndrome 6 8.022
19
c UNP011 Uniparental Disomy of Chromosome 14 15 7.629
20
MTR087 Maternal Uniparental Disomy 27 7.629
21
P ERL057 Early Infantile Epileptic Encephalopathy 61 7.184
22
P PTT014 Pitt-Hopkins Syndrome 63 7.061
23
DRV001 Dravet Syndrome 70 7.061
24
CHR174 Christianson Syndrome 47 6.995
25
CHR390 Chromosome 14q11-Q22 Deletion Syndrome 35 6.995
26
BRX001 Bruxism 51 6.995
27
LBS001 Lubs X-Linked Mental Retardation Syndrome 49 6.953
28
MWT001 Mowat-Wilson Syndrome 57 6.953
29
P NRN021 Neuronal Ceroid Lipofuscinosis 64 6.953
30
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 58 6.898
31
P PRV006 Pervasive Developmental Disorder 52 6.898
32
P RTN008 Retinitis Pigmentosa 79 6.766
33
c DFN179 Deafness, Autosomal Recessive 62 29 6.766
34
INF033 Infancy Electroclinical Syndrome 22 6.766
35
c ATS203 Autosomal Dominant Non-Syndromic Intellectual Disability 45 6.766
36
c DFN173 Deafness, Autosomal Recessive 40 25 6.766
37
c DFN030 Deafness, Autosomal Recessive 55 25 6.766
38
c FML346 Familial Adenomatous Polyposis 1 65 6.766
39
PHY002 Physical Disorder 41 6.766
40
GND018 Gene Duplication Disease 23 6.766
41
P PRV002 Periventricular Nodular Heterotopia 52 6.766
42
c CNG031 Congenital Nervous System Abnormality 24 6.766
43
GTP001 Gait Apraxia 28 6.766
44
PDC003 Pediculus Humanus Corporis Infestation 22 6.766
45
P ENC018 Encephalopathy 62 3.618
46
P HYP265 Hypotonia 42 3.254
47
P MVM001 Movement Disease 61 3.080
48
P EPL164 Epilepsy 70 2.658
49
P SZR006 Seizure Disorder 69 2.656
50
MCH006 Mechanical Strabismus 40 2.427
51
GLB002 Glioblastoma 67 2.304
52
P DYS154 Dystonia 64 2.240
53
HLX001 Helix Syndrome 47 2.221
54
CRP032 Corpus Callosum, Agenesis of 49 2.122
55
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 2.104
56
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.759
57
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 1.718
58
BRN028 Brain Cancer 73 1.718
59
GLM045 Glioma 62 1.718
60
GLL048 Glial Tumor 52 1.718
61
c RNG029 Ring Chromosome 14 Syndrome 31 1.697
62
P RNG032 Ring Chromosome 39 1.697
63
P LNG032 Lung Cancer 98 1.692
64
P OVR042 Ovarian Cancer 88 1.573
65
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 64 1.534
66
P HPT023 Hepatocellular Carcinoma 95 1.441
67
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.425
68
HPT022 Hepatoblastoma 54 1.425
69
c ATS007 Autism Spectrum Disorder 72 1.408
70
P SCL018 Scoliosis 57 1.335
71
P SLP005 Sleep Disorder 62 1.315
72
SQM006 Squamous Cell Carcinoma 59 1.293
73
ATH004 Athetosis 25 1.270
74
CLB010 Coloboma of Macula 53 1.146
75
P LKM002 Leukemia 66 1.084
76
c LKM061 Leukemia, Acute Myeloid 83 1.084
77
P MYL006 Myeloid Leukemia 60 1.084
78
P RTN024 Retinoblastoma 72 1.052
79
P CLR023 Colorectal Cancer 100 1.052
80
DMY004 Demyelinating Disease 50 1.052
81
BRN032 Brain Glioma 45 1.030
82
HGH043 High Grade Glioma 46 1.030
83
NNS045 Non-Specific Syndromic Intellectual Disability 41 1.030
84
AGN016 Aging 54 1.008
85
P SNS001 Sensorineural Hearing Loss 59 1.008
86
c RTN114 Retinitis Pigmentosa 58 40 1.008
87
MDD011 Mood Disorder 62 1.008
88
P OVR082 Overgrowth Syndrome 42 1.008
89
c BRN108 Branchiootic Syndrome 1 63 0.984
90
CRV035 Cervical Cancer 72 0.984
91
QDR001 Quadriplegia 49 0.984
92
PCH002 Pachygyria 32 0.984
93
TLN003 Telangiectasis 51 0.958
94
CRB159 Cerebral Visual Impairment 34 0.958
95
c RTN041 Retinitis Pigmentosa 11 43 0.930
96
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.898
97
P ANG001 Angelman Syndrome 65 0.898
98
P AGN002 Agnosia 53 0.898
99
P MYP006 Myopia 55 0.897
100
P PRS040 Prostate Cancer 95 0.871
101
P MCH002 Machado-Joseph Disease 63 0.863
102
c SML038 Small Cell Cancer of the Lung 69 0.863
103
P ENC054 Encephalopathy, Neonatal Severe, Due to Mecp2 Mutations 35 0.863
104
P HMN010 Hemangioma 61 0.863
105
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.863
106
P KLL001 Kallmann Syndrome 65 0.863
107
P NRF002 Neurofibromatosis 60 0.863
108
c CRT089 Cortical Dysplasia, Complex, with Other Brain Malformations 10 39 0.821
109
FCL014 Focal Epilepsy 53 0.821
110
P MGL030 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 46 0.821
111
ADL002 Adult Syndrome 69 0.768
112
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.768
113
CSY001 C Syndrome 61 0.768
114
VSL002 Visual Epilepsy 39 0.768
115
ANC002 Anca-Associated Vasculitis 44 0.768
116
ESP021 Esophageal Cancer 84 0.766
117
PRS025 Presbyopia 39 0.766
118
P BRS047 Breast Cancer 97 0.681
119
P PNC035 Pancreatic Cancer 86 0.681
120
P PRK039 Parkinsonism 55 0.634
121
DNN002 Donnai-Barrow Syndrome 54 0.634
122
RTN017 Retinal Detachment 60 0.634
123
SCL014 Scleral Staphyloma 22 0.634
124
P LNG064 Lung Cancer Susceptibility 3 70 0.577
125
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.551
126
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.551
127
P LNG021 Lung Occult Small Cell Carcinoma 20 0.551
128
P PLC011 Pilocytic Astrocytoma 55 0.482
129
IQS001 Iqsec2 19 0.418
130
P GST053 Gastric Cancer 82 0.390
131
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 0.390
132
P TMR010 Tumor Predisposition Syndrome 69 0.390
133
ADN011 Adenoid Cystic Carcinoma 68 0.390
134
BLD173 Bladder Small Cell Carcinoma 44 0.390
135
END057 Endometrial Cancer 71 0.390
136
ADN089 Adenosquamous Lung Carcinoma 49 0.390
137
SKN022 Skin Squamous Cell Carcinoma 54 0.390
138
LNG039 Lung Squamous Cell Carcinoma 57 0.390
139
GST040 Gastric Adenocarcinoma 66 0.390
140
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 0.390
141
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.390
142
UND011 Undetermined Early-Onset Epileptic Encephalopathy 46 0.373
143
OHT001 Ohtahara Syndrome 39 0.373
144
P DVL113 Developmental and Epileptic Encephalopathy 45 0.349
145
CLF027 Cleft Palate, Isolated 64 0.323
146
CHR103 Charge Syndrome 65 0.295
147
P HNT016 Huntington Disease 73 0.295
148
DGR001 Digeorge Syndrome 62 0.264
149
P NNS032 Non-Syndromic X-Linked Intellectual Disability 46 0.264
150
P BLD134 Bladder Cancer 79 0.229
151
c DVL052 Developmental and Epileptic Encephalopathy 26 37 0.229
153
NRL016 Neural Tube Defects 81 0.229
154
c CRN134 Cornelia De Lange Syndrome 2 31 0.229
155
c DVL029 Developmental and Epileptic Encephalopathy 2 46 0.229
156
c DVL035 Developmental and Epileptic Encephalopathy 4 38 0.229
157
P CRN015 Cornelia De Lange Syndrome 67 0.229
158
STX005 Stxbp1 Encephalopathy 23 0.229
159
STX004 Stxbp1 Encephalopathy with Epilepsy 14 0.229
160
CRP035 Corpus Callosum, Partial Agenesis of, X-Linked 38 0.187
161
c DVL058 Developmental and Epileptic Encephalopathy 32 27 0.187
162
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.187
163
CMB007 Combined Immunodeficiency 56 0.187
164
MNT237 Mental Retardation with Language Impairment and with or Without Autistic Features 41 0.187
165
c DVL041 Developmental and Epileptic Encephalopathy 13 43 0.187
166
SPS004 Spastic Quadriplegia 39 0.187
167
P ADN016 Adenocarcinoma 63 0.187
168
SVR004 Severe Combined Immunodeficiency 71 0.187
169
CRB037 Cerebral Palsy 67 0.187
170
P BNG026 Benign Neonatal Seizures 49 0.187
171
BNG006 Benign Familial Neonatal Epilepsy 54 0.187
172
P TRT010 Teratoma 50 0.187
173
SPS057 Spasticity 43 0.187
174
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.187
175
CLF001 Cleft Lip 54 0.187
176
CDK006 Cdkl5 Deficiency Disorder 30 0.187
177
P ENC004 Encephalitis 61 0.187
178
CNV009 Convulsions Benign Familial Neonatal Dominant Form 31 0.187
179
MYC069 Myoclonic-Astastic Epilepsy 43 0.187
180
P ALZ034 Alzheimer Disease 87 0.132
181
c EPS035 Episodic Ataxia, Type 2 63 0.132
182
LYM133 Lymphoma, Hodgkin, Classic 74 0.132
183
c OTP006 Otopalatodigital Syndrome, Type I 60 0.132
184
P EPL140 Epilepsy, Idiopathic Generalized 60 0.132
185
P EPL198 Epilepsy, Myoclonic Juvenile 61 0.132
186
EPL131 Epilepsy, Pyridoxine-Dependent 45 0.132
187
c CRD183 Ceroid Lipofuscinosis, Neuronal, 2 56 0.132
188
P MNT135 Mental Retardation, X-Linked, Syndromic 13 49 0.132
189
c DVL027 Developmental and Epileptic Encephalopathy 9 45 0.132
190
c CRD185 Ceroid Lipofuscinosis, Neuronal, 6 54 0.132
191
P LKM062 Leukemia, Acute Lymphoblastic 69 0.132
192
c DVL039 Developmental and Epileptic Encephalopathy 11 41 0.132
193
c DVL033 Developmental and Epileptic Encephalopathy 1 49 0.132
194
c WRB002 Warburg Micro Syndrome 1 51 0.132
195
c HLP022 Holoprosencephaly 8 22 0.132
196
c PNT036 Pontocerebellar Hypoplasia, Type 6 46 0.132
197
c SPN264 Spinocerebellar Ataxia, Autosomal Recessive 12 37 0.132
198
DSN002 Desanto-Shinawi Syndrome 35 0.132
199
MNT266 Mental Retardation and Distinctive Facial Features with or Without Cardiac Defects 30 0.132
200
NRD091 Neurodevelopmental Disorder with Hypotonia and Impaired Expressive Language and with or Without Seizures 28 0.132
201
c MNT337 Mental Retardation, Autosomal Dominant 58 23 0.132
202
c DVL059 Developmental and Epileptic Encephalopathy 33 34 0.132
203
MYC071 Myoclonic-Atonic Epilepsy 32 0.132
204
c DVL078 Developmental and Epileptic Encephalopathy 54 26 0.132
205
DYS001 Dyskinetic Cerebral Palsy 31 0.132
206
SCH074 Schuurs-Hoeijmakers Syndrome 48 0.132
207
P SML001 Small Cell Carcinoma 52 0.132
208
RSP023 Rasopathy 54 0.132
209
P KLF001 Kleefstra Syndrome 45 0.132
210
c ATR087 Atrial Standstill 1 74 0.132
211
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 0.132
212
HRT031 Hartnup Disorder 51 0.132
213
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 59 0.132
214
IMM167 Immune Deficiency Disease 77 0.132
215
P LYM118 Lymphoma 69 0.132
216
P FML011 Familial Adenomatous Polyposis 71 0.132
217
P WRB001 Warburg Micro Syndrome 41 0.132
218
SLT013 Salt and Pepper Syndrome 26 0.132
219
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 52 0.132
220
c BNG023 Benign Familial Infantile Epilepsy 57 0.132
221
c DVL067 Developmental and Epileptic Encephalopathy 42 34 0.132
222
c NNN027 Noonan Syndrome-Like Disorder with Loose Anagen Hair 2 42 0.132
223
c EPS048 Episodic Ataxia, Type 9 25 0.132
224
SYD002 Sydenham Chorea 34 0.132
225
SLT014 Salt and Pepper Developmental Regression Syndrome 43 0.132
226
c SZR007 Seizures, Benign Familial Infantile, 3 45 0.132
227
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 68 0.132
228
c EPL205 Epilepsy, Idiopathic Generalized 13 29 0.132
229
EPL206 Epilepsy, Progressive Myoclonic, 3, with or Without Intracellular Inclusions 30 0.132
230
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 0.132
231
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.132
232
ULN003 Ulnar-Mammary Syndrome 56 0.132
233
c DYS056 Dystonia 12 63 0.132
234
c DVL042 Developmental and Epileptic Encephalopathy 14 52 0.132
235
c CLR094 Ciliary Dyskinesia, Primary, 28 32 0.132
236
c DVL038 Developmental and Epileptic Encephalopathy 7 48 0.132
237
P CNG436 Congenital Disorder of Deglycosylation 51 0.132
238
EPL116 Epileptic Encephalopathy, Childhood-Onset 42 0.132
239
c TBR026 Tuberous Sclerosis 2 71 0.132
240
MNT320 Mental Retardation, Autosomal Dominant 6, with or Without Seizures 26 0.132
241
PHL006 Phelan-Mcdermid Syndrome 62 0.132
242
P FRG001 Fragile X Syndrome 70 0.132
243
c NRD032 Neurodegeneration with Brain Iron Accumulation 5 50 0.132
244
c EPL096 Epilepsy, Nocturnal Frontal Lobe, 5 32 0.132
245
SRC014 Sarcoma 64 0.132
246
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 62 0.132
247
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.132
248
c SCH079 Schizophrenia 1 44 0.132
249
c TBR025 Tuberous Sclerosis 1 84 0.132
250
P CHL002 Childhood Absence Epilepsy 63 0.132
251
c ATS387 Autosomal Dominant Non-Syndromic Intellectual Disability 5 34 0.132
252
c ATS388 Autosomal Dominant Non-Syndromic Intellectual Disability 6 32 0.132
253
TTH002 Tooth Agenesis 61 0.132
254
MNN009 Meningoencephalitis 48 0.132
255
LPD008 Lipid Metabolism Disorder 61 0.132
256
P CCK001 Cockayne Syndrome 68 0.132
257
PRP016 Paraplegia 52 0.132
258
P BNG030 Benign Ependymoma 51 0.132
259
c BSL007 Basal Cell Carcinoma 68 0.132
260
c HRD010 Hereditary Spastic Paraplegia 65 0.132
261
P HYP086 Hypothyroidism 69 0.132
262
c DLT002 Dilated Cardiomyopathy 79 0.132
263
P RHB003 Rhabdomyosarcoma 66 0.132
264
HMT002 Hematologic Cancer 61 0.132
265
RFL002 Reflex Epilepsy 40 0.132
266
c MCP050 Mucopolysaccharidosis, Type Ii 73 0.132
267
SPN035 Spindle Cell Sarcoma 51 0.132
268
c PRM212 Primary Microcephaly 40 0.132
269
c DVL053 Developmental and Epileptic Encephalopathy 27 29 0.132
270
MLG120 Malignant Migrating Partial Seizures of Infancy 44 0.132
271
P NRB001 Neuroblastoma 66 0.132
273
HYP266 Hypoxia 56 0.132
274
CLL010 Cellular Ependymoma 58 0.132
275
CLR030 Clear Cell Renal Cell Carcinoma 54 0.132
276
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.132
277
c LRG001 Large Cell Carcinoma 48 0.132
278
BLT001 Bilateral Retinoblastoma 35 0.132
281
MBD001 Mbd5 Haploinsufficiency 41 0.132
283
VNZ002 Venezuelan Equine Encephalitis 46 0.132
284
c EPL009 Epilepsy Progressive Myoclonic Type 3 19 0.132
285
EXN003 Exencephaly 30 0.132
286
PLG004 Plagiocephaly 40 0.132
289
CLF004 Cleft Lip/palate 57 0.132
290
XLN236 X-Linked Intellectual Disability-Epilepsy Syndrome 22 0.132
291
c RRP028 Rare Epilepsy 17 0.132
292
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 41 0.132
293
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.132
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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