Search results for dgcr8

191 hits were found for dgcr8

# Family MCID Name MIFTS Score
1
DGR001 Digeorge Syndrome 62 22.375
2
VLC001 Velocardiofacial Syndrome 57 18.611
3
P MLT008 Multinodular Goiter 41 12.514
4
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 9.045
5
P FRG001 Fragile X Syndrome 70 8.132
6
P CHR084 Chromosomal Disease 35 8.132
7
c CHR565 Chromosomal Deletion Syndrome 27 8.132
8
XLN191 X-Linked Hereditary Ataxia 20 8.132
9
DSS008 Disease of Mental Health 74 8.132
10
ORL003 Oral Tuberculosis 36 8.132
11
P BRS047 Breast Cancer 97 2.286
12
P SCH015 Schizophrenia 74 2.264
13
P SKN015 Skin Carcinoma 71 1.742
14
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.697
15
P PRS040 Prostate Cancer 95 1.604
16
P VNT002 Ventricular Septal Defect 58 1.507
17
HRT011 Heart Septal Defect 49 1.507
18
P OVR042 Ovarian Cancer 88 1.433
19
GLM045 Glioma 62 1.433
20
GLL048 Glial Tumor 51 1.433
21
AZS001 Azoospermia 45 1.368
22
P DNG005 Dengue Virus 55 1.291
23
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.291
24
CLR030 Clear Cell Renal Cell Carcinoma 53 1.261
25
ANV001 Anovulation 46 1.193
26
47X002 47,xyy 47 1.134
27
P TTR001 Tetralogy of Fallot 69 1.090
28
P BND020 Bone Disease 60 1.090
29
OST012 Osteoarthritis 77 1.090
30
CNT061 Conotruncal Heart Malformations 66 1.040
31
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.040
32
P SPR119 Spermatogenic Failure, X-Linked, 1 36 1.040
33
BRS099 Breast Ductal Carcinoma 61 1.040
34
c HPT016 Hepatitis B 62 1.040
35
P INF032 Infertility 60 1.040
36
THY029 Thyroid Carcinoma 55 1.040
37
c GLC092 Glaucoma, Primary Open Angle 60 1.013
38
P RTT002 Rett Syndrome 79 1.013
39
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.013
40
BNR002 Bone Resorption Disease 47 1.013
41
NRL002 Neurilemmomatosis 52 1.013
42
GTR002 Goiter 52 1.013
43
P OPN001 Open-Angle Glaucoma 55 1.013
44
c PRC016 Pre-Eclampsia 64 1.013
45
P PLR004 Pleuropulmonary Blastoma 65 0.983
46
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.983
47
PST011 Pustulosis of Palm and Sole 52 0.983
48
P PSR002 Psoriasis 63 0.983
49
DCR010 Dicer1 Tumor Predisposition 31 0.983
51
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.950
52
c SPN225 Spondyloarthropathy 1 70 0.950
53
P MLT020 Multiple Sclerosis 79 0.950
54
P SNS001 Sensorineural Hearing Loss 60 0.950
55
LVR012 Liver Cirrhosis 62 0.950
56
SPN051 Spondylitis 51 0.950
57
HYD002 Hydronephrosis 58 0.950
58
INF009 Inflammatory Spondylopathy 30 0.950
59
SDD008 Sudden Sensorineural Hearing Loss 41 0.950
60
P PNC035 Pancreatic Cancer 87 0.920
61
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.913
62
P PNB001 Pineoblastoma 49 0.913
63
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.913
64
P TRM003 Tremor 50 0.913
65
c WLM013 Wilms Tumor 1 65 0.868
66
P MLN007 Male Infertility 56 0.868
67
SKN013 Skin Benign Neoplasm 49 0.829
68
c MCR115 Microvascular Complications of Diabetes 5 65 0.811
69
MYL005 Myelofibrosis 70 0.551
70
P GST053 Gastric Cancer 82 0.342
71
P LNG032 Lung Cancer 98 0.342
72
c ATS007 Autism Spectrum Disorder 71 0.312
73
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.312
74
c SML038 Small Cell Cancer of the Lung 68 0.312
75
P BLD134 Bladder Cancer 79 0.312
76
HMN047 Human Cytomegalovirus Infection 59 0.312
77
ISC004 Ischemia 61 0.312
78
P HYP086 Hypothyroidism 68 0.312
79
P ESP024 Esophagitis 60 0.312
80
c HNT011 Huntington Disease-Like 3 33 0.279
81
c HNT004 Huntington Disease-Like 2 51 0.279
82
EWN003 Ewing Sarcoma 69 0.279
83
HLX001 Helix Syndrome 47 0.279
84
DFF005 Diffuse Large B-Cell Lymphoma 55 0.279
85
P KDN018 Kidney Disease 71 0.279
86
HYP066 Hyperglycemia 60 0.279
87
GST033 Gestational Diabetes 60 0.279
88
P BCL017 B-Cell Lymphoma 57 0.279
89
END086 End Stage Renal Disease 54 0.279
90
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.242
91
c MJR022 Major Affective Disorder 8 37 0.242
92
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 0.242
93
SMT008 Smith-Magenis Syndrome 53 0.242
94
c MJR024 Major Affective Disorder 9 40 0.242
95
THY111 Thyroid Carcinoma, Familial Medullary 67 0.242
96
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.242
97
P LRY044 Larynx Cancer 53 0.242
98
P BPL003 Bipolar Disorder 56 0.242
99
P PLM036 Pulmonary Fibrosis 65 0.242
100
THY125 Thyroid Gland Medullary Carcinoma 48 0.242
101
P DMN002 Dementia 65 0.242
102
P ENC004 Encephalitis 61 0.242
103
ATH013 Atherosclerosis Susceptibility 63 0.197
104
DSS032 Disease by Infectious Agent 55 0.197
105
P MYC084 Mycobacterium Tuberculosis 1 68 0.197
106
c ATR087 Atrial Standstill 1 74 0.197
107
ATM095 Autoimmune Disease 61 0.197
108
c HYP836 Hypercholesterolemia, Familial, 1 73 0.197
109
ESP021 Esophageal Cancer 84 0.197
110
CRV035 Cervical Cancer 72 0.197
111
c SCH051 Schizophrenia 4 35 0.197
112
P LNG064 Lung Cancer Susceptibility 3 69 0.197
113
NNL006 Non-Alcoholic Steatohepatitis 54 0.197
114
OST015 Osteochondrodysplasia 60 0.197
115
SQM006 Squamous Cell Carcinoma 59 0.197
116
P OST001 Osteopetrosis 70 0.197
117
SVR004 Severe Combined Immunodeficiency 70 0.197
118
SCH012 Schizoaffective Disorder 49 0.197
119
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.197
120
P LVR013 Liver Disease 68 0.197
121
PSY004 Psychotic Disorder 66 0.197
122
c DLT002 Dilated Cardiomyopathy 79 0.197
123
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.197
124
P THR014 Thrombocytopenia 66 0.197
125
P MLN008 Melanoma 75 0.197
126
SKN019 Skin Melanoma 70 0.197
127
FTT001 Fatty Liver Disease 61 0.197
128
PST092 Posttransplant Acute Limbic Encephalitis 29 0.197
129
PRT251 Proteinuria, Chronic Benign 58 0.140
130
RNL077 Renal Fibrosis 46 0.140
131
P ALZ034 Alzheimer Disease 87 0.140
132
P ATS364 Autism 72 0.140
133
P MDL005 Medulloblastoma 75 0.140
134
NRL016 Neural Tube Defects 80 0.140
135
P RTN024 Retinoblastoma 72 0.140
136
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.140
137
ALC007 Alcohol Dependence 65 0.140
139
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.140
140
AGN016 Aging 53 0.140
141
HYP865 Hypogonadotropic Hypogonadism 25 with Anosmia 23 0.140
142
ADR016 Adrenal Cortical Carcinoma 61 0.140
143
P ATX030 Ataxia-Telangiectasia 80 0.140
144
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.140
145
KPS004 Kaposi Sarcoma 76 0.140
146
P LKM062 Leukemia, Acute Lymphoblastic 69 0.140
147
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.140
148
P PRK057 Parkinson Disease, Late-Onset 79 0.140
149
P HNT016 Huntington Disease 73 0.140
150
CLF027 Cleft Palate, Isolated 64 0.140
151
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.140
152
c ERL056 Early-Onset Parkinson's Disease 39 0.140
153
P PRK039 Parkinsonism 55 0.140
154
CLR109 Colorectal Adenocarcinoma 50 0.140
155
HND002 Hand, Foot and Mouth Disease 50 0.140
156
c HPT015 Hepatitis D 49 0.140
157
GLB002 Glioblastoma 67 0.140
158
PNL014 Pineal Gland Cancer 40 0.140
159
CRV038 Cervical Squamous Cell Carcinoma 56 0.140
160
ADN018 Adenoma 58 0.140
161
CKT002 Cakut 48 0.140
162
GST037 Gastroparesis 52 0.140
163
P KDN017 Kidney Cancer 60 0.140
164
SPR008 Supratentorial Primitive Neuroectodermal Tumor 42 0.140
165
THY030 Thyroid Gland Disease 50 0.140
166
PNL002 Pineal Parenchymal Tumor of Intermediate Differentiation 24 0.140
167
MTH009 Mouth Disease 57 0.140
168
SPN035 Spindle Cell Sarcoma 51 0.140
169
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.140
170
ADR004 Adrenal Cortical Adenocarcinoma 38 0.140
171
P RHB003 Rhabdomyosarcoma 66 0.140
172
ART016 Aortic Aneurysm 68 0.140
173
PLM014 Pleomorphic Adenoma 51 0.140
174
P GRV001 Graves' Disease 54 0.140
175
P HYP024 Hypoparathyroidism 55 0.140
176
SRC014 Sarcoma 64 0.140
177
ALV002 Alveolar Echinococcosis 56 0.140
178
TLN003 Telangiectasis 51 0.140
179
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.140
180
SKN016 Skin Disease 63 0.140
181
P MYT002 Myotonic Dystrophy 51 0.140
182
CLF001 Cleft Lip 54 0.140
183
DGN001 Degenerative Disc Disease 48 0.140
184
BCK006 Back Pain 43 0.140
185
PPL050 Papillary Tumor of the Pineal Region 32 0.140
186
P CRB059 Cerebellar Degeneration 36 0.140
187
PNC056 Pineocytoma 44 0.140
189
GNT083 Genetic Neurodegenerative Disease 9 0.140
190
IDP093 Idiopathic Gastroparesis 28 0.140
191
SPN186 Spinal Cord Injury 60 0.140
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