Search results for hepatocellular carcinoma, childhood-onset

219 hits were found for hepatocellular carcinoma, childhood-onset

# Family MCID Name MIFTS Score
1
CHL128 Childhood Hepatocellular Carcinoma 47 6.589
2
P HPT023 Hepatocellular Carcinoma 94 2.034
3
P HPT021 Hepatitis 75 0.705
4
SQM006 Squamous Cell Carcinoma 74 0.695
5
P ADN016 Adenocarcinoma 71 0.672
6
c HPT016 Hepatitis B 68 0.470
7
P THY032 Thyroiditis 56 0.437
8
c BLD140 Blood Group, I System 37 0.377
9
END072 Endotheliitis 46 0.376
10
c HPT001 Hepatitis C 73 0.360
11
P ESP024 Esophagitis 64 0.339
12
HPT082 Hepatic Adenomas, Familial 52 0.321
13
c HPT073 Hepatitis C Virus 73 0.288
14
PRS047 Prostatitis 59 0.277
15
P PNC044 Pancreatitis 64 0.273
16
P CRV039 Cervicitis 49 0.253
17
AGN016 Aging 65 0.207
18
PRT018 Portal Vein Thrombosis 50 0.195
19
P BRS047 Breast Cancer 100 0.193
20
c HPT003 Hepatitis a 63 0.189
21
P LYM118 Lymphoma 71 0.171
22
P KDN018 Kidney Disease 69 0.168
23
MLN008 Melanoma 72 0.167
24
P LPS004 Lupus Erythematosus 69 0.167
25
P LNG032 Lung Cancer 99 0.163
26
P CLR023 Colorectal Cancer 98 0.157
27
PRT036 Peritonitis 67 0.157
28
GST050 Gastrointestinal System Disease 66 0.151
29
P LKM002 Leukemia 75 0.150
30
P ANR048 Aniridia 1 68 0.145
31
ANR038 Anorexia Nervosa 1 21 0.145
32
BLD137 Blood Group--Ahonen 17 0.145
33
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.144
34
HPT022 Hepatoblastoma 55 0.134
35
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.132
36
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.131
37
CHR177 Chromophobe Renal Cell Carcinoma 59 0.131
38
ESP021 Esophageal Cancer 79 0.130
39
PPL022 Papilloma 58 0.128
40
P PRP029 Porphyria 62 0.126
41
P OVR042 Ovarian Cancer 82 0.125
42
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.125
43
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.125
44
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.125
45
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.125
46
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.125
47
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.125
48
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.125
49
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.125
50
P PNC035 Pancreatic Cancer 89 0.124
51
P OBS001 Obstructive Jaundice 53 0.124
52
PHR003 Pharyngitis 59 0.123
53
P RNL003 Renal Clear Cell Carcinoma 58 0.123
54
NRN002 Neuronitis 43 0.122
55
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.120
56
NNL002 Nonalcoholic Steatohepatitis 56 0.118
57
INS024 Insulin-Like Growth Factor I 83 0.116
58
P PRS040 Prostate Cancer 88 0.115
59
CRB009 Cerebritis 41 0.114
60
ALR002 Al-Raqad Syndrome 30 0.113
61
SRC014 Sarcoma 68 0.109
62
P ENC018 Encephalopathy 58 0.108
63
P DBT009 Diabetes Mellitus 72 0.107
64
DDN006 Duodenitis 46 0.106
65
END057 Endometrial Cancer 76 0.103
66
P ART022 Arthritis 77 0.101
67
RTN023 Retinitis 52 0.101
68
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.101
69
P PRM006 Primary Biliary Cirrhosis 55 0.100
70
P HMN010 Hemangioma 61 0.100
71
P INT068 Intestinal Disease 65 0.100
72
P HYP086 Hypothyroidism 62 0.100
73
c ATM011 Autoimmune Hepatitis 63 0.100
74
P HRP006 Herpes Simplex 70 0.099
75
HYP056 Hypoglycemia 62 0.099
76
P GLM045 Glioma 61 0.098
77
CHL067 Cholecystitis 58 0.097
78
P PNM007 Pneumonia 70 0.097
79
ISC004 Ischemia 66 0.096
80
MCS002 Mucositis 61 0.094
81
P CHL066 Cholangitis 52 0.094
82
P PRP003 Porphyria Cutanea Tarda 67 0.094
83
SPS003 Spastic Diplegia 55 0.092
84
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.089
85
c THR092 Thrombophilia Due to Thrombin Defect 61 0.089
86
BDD001 Budd-Chiari Syndrome 58 0.089
87
CLT003 Colitis 63 0.088
88
VCC001 Vaccinia 50 0.088
89
GST019 Gastrointestinal Stromal Tumor 74 0.087
90
NDL013 Nodular Regenerative Hyperplasia 53 0.086
91
ULC004 Ulcerative Colitis 80 0.085
92
P PLY041 Polymyositis 57 0.085
93
c TRC078 Trichohepatoenteric Syndrome 2 34 0.085
94
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.084
95
ALP103 Alpha-1-Antitrypsin Deficiency 60 0.084
96
P BCL006 B-Cell Lymphomas 70 0.082
97
GST040 Gastric Adenocarcinoma 60 0.082
98
P GST044 Gastritis 61 0.082
99
P THR014 Thrombocytopenia 65 0.081
100
ANR040 Aneurysm 61 0.079
101
P GLM007 Glomerulonephritis 61 0.079
102
c ACT027 Acute Pancreatitis 61 0.079
103
P PSR002 Psoriasis 65 0.079
104
VLV044 Vulvar Intraepithelial Neoplasia 40 0.078
105
PRP030 Purpura 61 0.077
106
P RHM011 Rheumatoid Arthritis 91 0.076
107
PYG006 Pyogenic Granuloma 45 0.076
108
P MYS005 Myositis 63 0.075
109
BLD163 Blood Group, Dombrock System 23 0.075
110
HST009 Histiocytoma 51 0.075
111
P AMY004 Amyloidosis 69 0.073
112
FBR003 Fibrous Histiocytoma 46 0.073
113
DRM006 Dermatitis 67 0.073
114
ANG020 Angiosarcoma 57 0.073
115
P PTY003 Pityriasis Rubra Pilaris 48 0.072
116
SCH014 Schistosomiasis 62 0.071
117
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 51 0.070
118
P PLY019 Polyneuropathy 58 0.069
119
P LFR001 Li-Fraumeni Syndrome 72 0.069
120
P AST007 Astrocytoma 66 0.068
121
VSC011 Vasculitis 66 0.068
122
c MLG068 Malignant Glioma 66 0.068
123
ORL004 Oral Submucous Fibrosis 56 0.067
124
P FBR017 Fibrosarcoma 61 0.066
125
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.066
126
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.066
127
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.066
128
P RHB003 Rhabdomyosarcoma 61 0.064
129
VRC005 Varicose Veins 64 0.064
130
ADN027 Adenomyosis 57 0.064
131
HYP066 Hyperglycemia 64 0.064
132
P HML002 Hemolytic Anemia 62 0.064
133
MYL069 Myeloma, Multiple 86 0.064
134
P PLY018 Polycythemia 60 0.064
135
P INT070 Intestinal Obstruction 55 0.063
136
P HYP076 Hyperthyroidism 56 0.062
137
PST011 Pustulosis of Palm and Sole 47 0.061
138
ADP007 Adie Pupil 41 0.061
139
P CND004 Candidiasis 61 0.061
140
CHL004 Cholelithiasis 51 0.061
141
RHM027 Rheumatic Disease 62 0.060
142
P ASP006 Aspergillosis 65 0.060
143
ALP046 Alport Syndrome, X-Linked 74 0.060
144
P HMP007 Hemophilia 61 0.059
145
BLM001 Bloom Syndrome 62 0.059
146
P ATM019 Autoimmune Polyendocrine Syndrome 47 0.059
147
CNN005 Connective Tissue Disease 65 0.059
148
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.059
149
END030 End Stage Renal Failure 59 0.059
150
ART016 Aortic Aneurysm 70 0.058
151
OVR063 Overnutrition 53 0.058
152
P CTN003 Cutaneous Lupus Erythematosus 53 0.057
153
P EPT020 Epithelioid Hemangioendothelioma 50 0.057
154
URM002 Uremia 52 0.057
155
P HRT032 Heart Disease 80 0.057
156
PRP016 Paraplegia 53 0.056
157
c XRD030 Xeroderma Pigmentosum, Complementation Group C 52 0.056
158
DFF005 Diffuse Large B-Cell Lymphoma 64 0.056
159
P NRV007 Nervous System Disease 75 0.056
160
c HMP029 Hemophilia a 69 0.056
161
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.056
162
OST003 Osteonecrosis 63 0.055
163
DSS009 Disseminated Intravascular Coagulation 56 0.055
164
SLD003 Sialadenitis 49 0.055
165
P DLT002 Dilated Cardiomyopathy 76 0.055
166
PLY020 Polyradiculoneuropathy 48 0.055
167
c ACT134 Acute Liver Failure 52 0.055
168
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.054
169
LMB062 Limb Ischemia 52 0.054
170
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 46 0.054
171
IRN001 Iron Deficiency Anemia 55 0.053
172
DFC004 Deficiency Anemia 62 0.053
173
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 46 0.053
174
PNC001 Pancytopenia 50 0.052
175
CTR172 Citrullinemia, Classic 58 0.052
176
CRY004 Cryoglobulinemia 49 0.052
177
ART012 Aortitis 33 0.051
178
ATM095 Autoimmune Disease 66 0.051
179
P FRD012 Friedreich Ataxia 1 58 0.051
180
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.050
181
P WSK001 Wiskott-Aldrich Syndrome 76 0.050
182
CMM004 Common Variable Immunodeficiency 71 0.050
183
ACT029 Acute Interstitial Pneumonia 41 0.050
184
P MTR004 Maturity-Onset Diabetes of the Young 62 0.050
185
P GRF003 Graft-Versus-Host Disease 72 0.050
186
c ALZ056 Alzheimer Disease 3 41 0.050
187
P ANX007 Anauxetic Dysplasia 1 36 0.050
188
URT039 Urticaria 59 0.048
189
c PRC016 Pre-Eclampsia 65 0.047
190
MCR004 Macroglobulinemia 54 0.047
191
LRG008 Large Granular Lymphocyte Leukemia 49 0.047
192
SPL006 Splenic Infarction 34 0.047
193
SVN002 Sveinsson Chorioretinal Atrophy 29 0.047
194
P PNM006 Pneumoconiosis 55 0.047
195
c ACT159 Acute Transverse Myelitis 45 0.047
196
c PSR018 Psoriasis 13 39 0.047
197
P ECL001 Eclampsia 57 0.046
198
P TCL004 T-Cell Leukemia 50 0.046
199
P CRY007 Cryoglobulinemia, Familial Mixed 49 0.046
200
P SDR003 Sideroblastic Anemia 43 0.046
201
c CHL143 Cholestasis, Progressive Familial Intrahepatic, 4 21 0.046
202
P PRK057 Parkinson Disease, Late-Onset 78 0.046
203
ACR006 Aceruloplasminemia 65 0.046
204
P ART067 Aortic Aneurysm, Familial Thoracic 1 65 0.046
205
PRP027 Peripheral Vascular Disease 71 0.045
206
ENT004 Enthesopathy 38 0.045
207
CYS001 Cystic Fibrosis 85 0.044
208
MRB003 Morbid Obesity 61 0.044
209
P CLL015 Collagen Disease 53 0.044
210
GLC098 Glaucoma-Related Pigment Dispersion Syndrome 40 0.044
211
P ART023 Arthropathy 68 0.043
212
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 59 0.042
213
P ART084 Arteriovenous Fistula 46 0.042
214
NRR001 Neuroretinitis 46 0.042
215
FBL002 Fibular Hypoplasia and Complex Brachydactyly 40 0.040
216
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 37 0.040
217
HMN038 Human Coronavirus Sensitivity 17 0.040
218
P MGL013 Megalencephaly 54 0.038
219
c DNR003 Duane Retraction Syndrome 1 34 0.038
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