Search results for ANKRD11

253 hits were found for ANKRD11

# Family MCID Name MIFTS Score
1
KBG001 Kbg Syndrome 54 68.311
2
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 58.914
3
c ATS007 Autism Spectrum Disorder 72 40.827
4
DSS008 Disease of Mental Health 74 25.531
5
AST006 Astigmatism 47 21.154
6
RRG006 Rare Genetic Intellectual Disability 26 20.983
7
16Q001 16q24.3 Microdeletion Syndrome 27 18.036
8
CRY035 Cryptorchidism, Unilateral or Bilateral 58 17.456
9
HYP748 Hypertelorism 46 17.019
10
P ATS364 Autism 69 16.718
11
ABR009 Abruzzo-Erickson Syndrome 45 16.551
12
EPC005 Epicanthus 36 15.964
13
EST005 Esotropia 43 15.964
14
P PTS002 Ptosis 52 13.809
15
P SZR006 Seizure Disorder 70 12.075
16
P CFF008 Coffin-Siris Syndrome 1 64 11.907
17
P NRV007 Nervous System Disease 67 11.535
18
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 11.030
19
P CRN015 Cornelia De Lange Syndrome 67 10.304
20
FRS019 Farsightedness 36 8.810
21
P KBK002 Kabuki Syndrome 1 65 8.750
22
c MNT211 Mental Retardation, Autosomal Dominant 23 34 7.763
23
c ATS203 Autosomal Dominant Non-Syndromic Intellectual Disability 45 7.763
24
c RTN116 Retinitis Pigmentosa 56 26 7.154
25
c MRG011 Meier-Gorlin Syndrome 4 27 7.154
26
c CFF014 Coffin-Siris Syndrome 9 32 7.154
27
GLS018 Glass Syndrome 61 7.154
28
URT020 Ureterocele 36 7.154
29
c BRC108 Brachydactyly, Type A3 27 7.154
30
FML286 Familial Isolated Trichomegaly 29 7.154
31
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 3.695
32
c CRN139 Cornelia De Lange Syndrome 1 61 3.150
33
P BRC006 Brachydactyly 51 2.562
34
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 2.227
35
P THR014 Thrombocytopenia 66 2.227
36
GST103 Gastric Cancer, Hereditary Diffuse 68 2.226
37
LRN003 Learning Disability 49 2.097
38
P BRS047 Breast Cancer 98 2.006
39
SML009 Small Intestine Adenocarcinoma 57 1.995
40
c OTP006 Otopalatodigital Syndrome, Type I 60 1.953
41
TTH002 Tooth Agenesis 61 1.953
42
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 68 1.953
43
P PRC019 Precocious Puberty 47 1.953
44
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 1.905
45
c CLR087 Colorectal Cancer 12 34 1.905
46
P OVR042 Ovarian Cancer 88 1.837
47
SML031 Small Cell Carcinoma of the Bladder 46 1.810
48
CLN015 Colon Adenocarcinoma 65 1.799
49
DRV001 Dravet Syndrome 69 1.790
50
CLF027 Cleft Palate, Isolated 64 1.790
51
WST001 West Syndrome 59 1.790
52
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 1.790
53
P SLV027 Silver-Russell Syndrome 1 52 1.790
54
P FBR031 Febrile Seizures 52 1.790
55
DNC004 Diencephalic Syndrome 36 1.790
56
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 1.730
57
CLF048 Cleft Palate, Psychomotor Retardation, and Distinctive Facial Features 28 1.597
58
P HYP265 Hypotonia 42 1.597
59
P GST053 Gastric Cancer 83 1.574
60
END057 Endometrial Cancer 72 1.543
61
P BLD134 Bladder Cancer 79 1.478
62
P LNG064 Lung Cancer Susceptibility 3 70 1.397
63
END041 Endometrial Adenocarcinoma 64 1.295
64
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 1.218
65
SPN439 Spondyloepimetaphyseal Dysplasia, Isidor-Toutain Type 20 1.218
66
SPN250 Spondyloepimetaphyseal Dysplasia 36 1.218
67
RHB001 Rhabdoid Cancer 68 1.218
68
PLM026 Pilomatrixoma 57 1.203
69
LNG039 Lung Squamous Cell Carcinoma 57 1.135
70
P PRS040 Prostate Cancer 95 1.100
71
PPL004 Papillary Squamous Carcinoma 39 1.064
72
GST092 Gastroesophageal Reflux 61 1.055
73
OTT002 Otitis Media 71 1.055
74
P STR020 Strabismus 56 1.055
75
P NNN008 Noonan Syndrome 1 77 1.055
76
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 1.055
77
BSL009 Basal Ganglia Calcification 45 1.055
78
P SCL018 Scoliosis 57 1.055
79
MCH006 Mechanical Strabismus 40 1.055
80
GNG013 Gingivitis 59 1.055
81
RFR003 Refractive Error 41 1.055
82
c PSD047 Pseudo-Turner Syndrome 52 1.055
83
GST040 Gastric Adenocarcinoma 67 1.026
84
BRS099 Breast Ductal Carcinoma 61 0.968
85
P RHB003 Rhabdomyosarcoma 66 0.951
86
P LNG032 Lung Cancer 98 0.905
87
c GLM047 Glioma Susceptibility 3 33 0.905
88
P TMR010 Tumor Predisposition Syndrome 67 0.905
89
c MSM022 Mismatch Repair Cancer Syndrome 1 70 0.905
90
c GLM025 Glioma Susceptibility 2 30 0.905
91
c GLM043 Glioma Susceptibility 9 30 0.905
92
P GLM040 Glioma Susceptibility 1 71 0.905
93
MNN043 Meningioma, Familial 79 0.905
94
ADN011 Adenoid Cystic Carcinoma 68 0.905
95
P OLG002 Oligodendroglioma 66 0.905
96
ADN089 Adenosquamous Lung Carcinoma 49 0.905
97
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.905
98
LBL001 Lobular Neoplasia 55 0.905
99
GLM045 Glioma 63 0.905
100
LPM012 Lipomatosis, Multiple 60 0.861
101
DWN001 Down Syndrome 70 0.861
102
P TTR001 Tetralogy of Fallot 69 0.861
103
HRT011 Heart Septal Defect 49 0.861
104
PLM005 Pleomorphic Lipoma 40 0.861
105
P ATR010 Atrial Heart Septal Defect 58 0.861
106
HYD002 Hydronephrosis 58 0.861
107
P TCD001 Tic Disorder 49 0.861
108
c JVN010 Juvenile Rheumatoid Arthritis 66 0.861
109
CHR178 Chromosomal Triplication 34 0.861
110
ESP021 Esophageal Cancer 83 0.861
111
EWN003 Ewing Sarcoma 70 0.834
112
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 0.790
113
SKN022 Skin Squamous Cell Carcinoma 54 0.790
114
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 0.790
115
MLD018 Mild Cognitive Impairment 48 0.735
116
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.684
117
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 21 0.684
118
MTR087 Maternal Uniparental Disomy 28 0.609
119
P THL005 Thalassemia 56 0.609
120
P OVR082 Overgrowth Syndrome 49 0.609
121
P ALZ034 Alzheimer Disease 87 0.609
122
ATH013 Atherosclerosis Susceptibility 63 0.609
123
P NSP012 Nasopharyngeal Carcinoma 61 0.609
124
c ATS268 Autism X-Linked 4 24 0.609
125
RBR002 Roberts-Sc Phocomelia Syndrome 63 0.609
126
PRX085 Preaxial Hallucal Polydactyly 28 0.609
127
c ALP101 Alpha-Thalassemia 62 0.609
128
MRF001 Marfan Syndrome 76 0.609
129
OBS002 Obsessive-Compulsive Disorder 68 0.609
130
P LYS001 Loeys-Dietz Syndrome 65 0.609
131
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 0.609
132
INT072 Intestinal Pseudo-Obstruction 62 0.609
133
c BRN108 Branchiootic Syndrome 1 62 0.609
134
CHR515 Chronic Atrial and Intestinal Dysrhythmia 43 0.609
135
CHP002 Chops Syndrome 47 0.609
136
WRS002 Warsaw Breakage Syndrome 46 0.609
137
CHR621 Chromosome 16p11.2 Deletion Syndrome, 593-Kb 27 0.609
138
PSD014 Pseudopseudohypoparathyroidism 54 0.609
139
CRN320 Cornelia De Lange Syndrome 3 with or Without Midline Brain Defects 40 0.609
140
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.609
141
P PTN014 Patent Ductus Arteriosus 1 59 0.609
142
RNL077 Renal Fibrosis 46 0.609
143
ALP095 Alpha Thalassemia-X-Linked Intellectual Disability Syndrome 44 0.609
144
P KDN018 Kidney Disease 72 0.609
145
CRC021 Carcinosarcoma 64 0.609
146
c UNP012 Uniparental Disomy of Chromosome 7 14 0.609
147
ACR013 Acrodysostosis 51 0.609
148
P VNT002 Ventricular Septal Defect 58 0.609
149
P EPL164 Epilepsy 68 0.609
150
CHR498 Chromosome 16p11.2 Duplication Syndrome 27 0.609
151
P HRT032 Heart Disease 81 0.609
152
UTR024 Uterine Carcinosarcoma 59 0.609
153
P SCK002 Sick Sinus Syndrome 55 0.609
154
HYP014 Hyperuricemia 51 0.609
155
KLD004 Keloid Disorder 39 0.609
156
16P010 16p11.2 Recurrent Microdeletion 7 0.609
158
WRS003 Warsaw Syndrome 11 0.609
159
P TRC031 Trichorhinophalangeal Syndrome 38 0.609
160
IQS001 Iqsec2 18 0.609
161
CNG134 Congenitally Corrected Transposition of the Great Arteries 38 0.609
162
P ATS382 Autosomal Dominant Tubulointerstitial Kidney Disease 34 0.609
163
DBL004 Double Discordia 20 0.609
164
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.592
165
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.592
166
P BLD062 Bile Duct Cancer 67 0.592
167
P LNG021 Lung Occult Small Cell Carcinoma 20 0.592
168
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.592
169
MRK001 Merkel Cell Carcinoma 64 0.592
170
c PRS097 Prostate Cancer, Hereditary, 1 39 0.523
171
c PRS070 Prostate Cancer, Hereditary, 12 22 0.523
172
c PRS071 Prostate Cancer, Hereditary, 13 25 0.523
173
c PRS117 Prostate Cancer, Hereditary, 11 24 0.523
174
c PRS114 Prostate Cancer, Hereditary, 2 33 0.523
175
ESP027 Esophagus Squamous Cell Carcinoma 45 0.523
176
PRS015 Prostate Signet Ring Cell Adenocarcinoma 25 0.523
177
P PNC035 Pancreatic Cancer 86 0.492
178
P LKM062 Leukemia, Acute Lymphoblastic 69 0.492
179
CLL010 Cellular Ependymoma 57 0.492
180
VNH007 Von Hippel-Lindau Syndrome 73 0.484
181
MLT165 Multilocular Cystic Renal Neoplasm of Low Malignant Potential 28 0.484
182
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 32 0.484
183
OVR062 Ovary Serous Adenocarcinoma 25 0.484
184
PRM126 Primary Peritoneal Carcinoma 62 0.484
185
CLR030 Clear Cell Renal Cell Carcinoma 54 0.484
186
END032 Endometrial Clear Cell Adenocarcinoma 34 0.395
187
CRC045 Carcinoma of Gallbladder and Extrahepatic Biliary Tract 21 0.342
188
SQM016 Squamous Cell Carcinoma of Gallbladder and Extrahepatic Biliary Tract 16 0.342
189
IRN008 Iron Overload in Africa 51 0.342
190
RNL119 Renal Cell Carcinoma, Xp11-Associated 42 0.342
191
SRC027 Sarcoma, Synovial 58 0.342
192
P RTH006 Rothmund-Thomson Syndrome, Type 2 67 0.342
193
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.342
194
RMB001 Rombo Syndrome 30 0.342
195
P LFR001 Li-Fraumeni Syndrome 73 0.342
196
THY121 Thyroid Gland Anaplastic Carcinoma 67 0.342
197
HPT079 Hepatoid Adenocarcinoma 39 0.342
198
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.342
199
P TRC095 Trichoepithelioma, Multiple Familial, 1 32 0.342
200
WRN001 Werner Syndrome 69 0.342
201
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.342
202
c BSL024 Basal Cell Carcinoma 1 55 0.342
203
BSL044 Basal Cell Carcinoma, Infundibulocystic 35 0.342
204
RJS001 Ruijs-Aalfs Syndrome 47 0.342
205
c BSL034 Basal Cell Carcinoma 7 26 0.342
206
c HPT073 Hepatitis C Virus 71 0.342
207
c RHB023 Rhabdomyosarcoma, Embryonal, 1 45 0.342
208
RHB024 Rhabdomyosarcoma 2 67 0.342
209
DRM014 Dermatofibrosarcoma Protuberans 65 0.342
210
c RHB021 Rhabdomyosarcoma, Embryonal, 2 24 0.342
211
P HPT023 Hepatocellular Carcinoma 96 0.342
212
c ALB010 Albinism, Oculocutaneous, Type Ib 52 0.342
213
GST019 Gastrointestinal Stromal Tumor 78 0.342
214
BNS007 Bone Sarcoma 51 0.342
215
PDT042 Pediatric Hepatocellular Carcinoma 49 0.342
216
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.342
217
CYS004 Cystic Basal Cell Carcinoma 36 0.342
218
SRC003 Sarcomatoid Basal Cell Carcinoma 28 0.342
219
NDL009 Nodular Basal Cell Carcinoma 40 0.342
220
MTT001 Metatypical Basal Cell Carcinoma 32 0.342
221
PGM002 Pigmented Basal Cell Carcinoma 31 0.342
222
MCR016 Micronodular Basal Cell Carcinoma 34 0.342
223
INF027 Infiltrative Basal Cell Carcinoma 32 0.342
224
ANL013 Anal Margin Basal Cell Carcinoma 18 0.342
225
SBC013 Sebaceous Basal Cell Carcinoma 13 0.342
226
ADM002 Adamantinoid Basal Cell Epithelioma 20 0.342
227
CLR015 Clear Cell Basal Cell Carcinoma 39 0.342
228
ADN015 Adenoid Basal Cell Carcinoma 31 0.342
229
CLR005 Clear Cell Chondrosarcoma 37 0.342
230
DST001 Distal Biliary Tract Carcinoma 24 0.342
231
P MSN005 Mesenchymal Chondrosarcoma 47 0.342
232
MTN001 Metanephric Adenoma 40 0.342
233
SGN001 Signet Ring Basal Cell Carcinoma 32 0.342
234
ANG020 Angiosarcoma 64 0.342
235
LVR002 Liver Angiosarcoma 43 0.342
236
c BSL007 Basal Cell Carcinoma 68 0.342
237
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.342
238
ADL096 Adult Hepatocellular Carcinoma 60 0.342
239
FBR086 Fibrolamellar Carcinoma 59 0.342
240
HPT011 Hepatocellular Clear Cell Carcinoma 46 0.342
241
PNS010 Penis Squamous Cell Carcinoma 45 0.342
242
PRS008 Prostate Small Cell Carcinoma 25 0.342
243
PNS005 Penis Mixed Squamous Cell Carcinoma 12 0.342
244
SPN009 Spindle Cell Rhabdomyosarcoma 39 0.342
245
P LPS002 Liposarcoma 64 0.342
246
SQM006 Squamous Cell Carcinoma 60 0.342
247
KPS002 Kaposiform Hemangioendothelioma 50 0.342
248
9Q2001 9q22.3 Microdeletion 24 0.342
249
NNN007 Non-Involuting Congenital Hemangioma 40 0.342
250
RCS008 Recessive Dystrophic Epidermolysis Bullosa-Generalized Other 30 0.342
251
INF057 Inflammatory Linear Verrucous Epidermal Nevus 33 0.342
252
LNR004 Linear Porokeratosis 33 0.342
253
PTY007 Pityriasis Rotunda 26 0.342
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