Search results for hepatocellular carcinoma, childhood-onset

163 hits were found for hepatocellular carcinoma, childhood-onset

# Family MCID Name MIFTS Score
1
CHL128 Childhood Hepatocellular Carcinoma 30 5.824
2
SQM006 Squamous Cell Carcinoma 70 0.549
3
P ADN016 Adenocarcinoma 69 0.470
4
END072 Endotheliitis 42 0.313
5
ORL015 Oral Squamous Cell Carcinoma 57 0.252
6
P PNC044 Pancreatitis 61 0.223
7
P NSP012 Nasopharyngeal Carcinoma 66 0.219
8
CLR030 Clear Cell Renal Cell Carcinoma 53 0.169
9
DCT002 Ductal Carcinoma in Situ 51 0.169
10
P GST049 Gastrointestinal System Cancer 60 0.157
11
MCP006 Mucoepidermoid Carcinoma 48 0.155
12
CRV038 Cervical Squamous Cell Carcinoma 60 0.152
13
P LPS004 Lupus Erythematosus 64 0.150
14
ADN009 Adenosquamous Carcinoma 51 0.147
15
INT079 Intrahepatic Cholangiocarcinoma 56 0.147
16
ORL011 Oral Cancer 56 0.145
17
OCL009 Ocular Cancer 59 0.134
18
GST053 Gastric Cancer 78 0.133
19
ACD009 Acid-Labile Subunit, Deficiency of 45 0.133
20
c CLL013 Cell Type Cancer 46 0.128
21
P OBS005 Obesity 92 0.128
22
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.126
23
P LNG032 Lung Cancer 95 0.123
24
LNG039 Lung Squamous Cell Carcinoma 54 0.123
25
c INS002 in Situ Carcinoma 53 0.118
26
ESP021 Esophageal Cancer 76 0.115
27
P PRP029 Porphyria 59 0.114
28
P PNC035 Pancreatic Cancer 87 0.109
29
ALR002 Al-Raqad Syndrome 36 0.109
30
GRW007 Growth Hormone Deficiency 50 0.107
31
c THR092 Thrombophilia Due to Thrombin Defect 54 0.106
32
NRN002 Neuronitis 41 0.105
33
INS024 Insulin-Like Growth Factor I 75 0.104
34
P LNG064 Lung Cancer Susceptibility 3 62 0.104
35
P ATX004 Ataxia 53 0.101
36
P OVR042 Ovarian Cancer 76 0.101
37
PHR003 Pharyngitis 56 0.101
38
INT253 Intestinal Benign Neoplasm 47 0.099
39
CRB009 Cerebritis 39 0.096
40
HPT074 Hepatic Adenoma, Somatic 50 0.094
41
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.094
42
NTR005 Nutritional Deficiency Disease 36 0.093
43
P FML011 Familial Adenomatous Polyposis 68 0.092
44
P CRV031 Cervical Adenocarcinoma 53 0.091
45
CLR109 Colorectal Adenocarcinoma 51 0.091
46
URN008 Urinary Bladder Cancer 66 0.090
47
P OVR049 Ovarian Disease 56 0.089
48
CRN036 Craniopharyngioma 59 0.088
49
RTN023 Retinitis 50 0.087
50
P ART022 Arthritis 75 0.087
51
PNC033 Pancreas Adenocarcinoma 57 0.086
52
GST050 Gastrointestinal System Disease 56 0.085
53
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.083
54
P PRP003 Porphyria Cutanea Tarda 64 0.083
55
HYP056 Hypoglycemia 61 0.081
56
FML039 Female Reproductive System Disease 48 0.081
57
c TRC078 Trichohepatoenteric Syndrome 2 29 0.081
58
P SPS003 Spastic Diplegia 52 0.080
59
PRP027 Peripheral Vascular Disease 68 0.080
60
CHL067 Cholecystitis 57 0.080
61
SKN023 Skin Tag 44 0.079
62
ALN001 Aland Island Eye Disease 45 0.078
63
ISC004 Ischemia 61 0.078
64
ACR041 Acromelic Frontonasal Dysostosis 45 0.078
65
BRT030 Birth Defects 43 0.078
66
SPC003 Specific Developmental Disorder 38 0.077
67
P GLM045 Glioma 60 0.077
68
P ENC018 Encephalopathy 59 0.077
69
END057 Endometrial Cancer 75 0.075
70
P PLY041 Polymyositis 52 0.073
71
GND003 Gonadal Disease 39 0.071
72
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.070
73
LRN003 Learning Disability 49 0.070
74
CRV047 Cervical Cancer, Somatic 65 0.070
75
HNM002 Hinman Syndrome 25 0.070
76
P RHM011 Rheumatoid Arthritis 89 0.070
77
GLL018 Gallbladder Cancer 63 0.070
78
P LFR001 Li-Fraumeni Syndrome 75 0.068
79
THY030 Thyroid Gland Disease 48 0.068
80
ANR040 Aneurysm 57 0.067
81
P HYP083 Hypopituitarism 54 0.066
82
PTY003 Pityriasis Rubra Pilaris 46 0.065
83
c ACT027 Acute Pancreatitis 57 0.065
84
CNN005 Connective Tissue Disease 62 0.065
85
KWS002 Kawasaki Disease 70 0.064
86
P GLM007 Glomerulonephritis 59 0.064
87
AND005 Androgen Insensitivity Syndrome, Mild 16 0.064
88
P MYS005 Myositis 57 0.063
89
P PRS038 Personality Disorder 62 0.063
90
P PSR002 Psoriasis 61 0.062
91
P GLB002 Glioblastoma 68 0.062
92
P INT068 Intestinal Disease 60 0.061
93
P HRT032 Heart Disease 75 0.061
94
VSC011 Vasculitis 62 0.061
95
c MLG002 Malignant Peritoneal Mesothelioma 46 0.059
96
END041 Endometrial Adenocarcinoma 56 0.059
97
SPC010 Speech and Communication Disorders 41 0.058
98
P TRN020 Turner Syndrome 65 0.058
99
P CRD011 Cardiomyopathy 68 0.058
100
PRP016 Paraplegia 49 0.058
101
OVR063 Overnutrition 50 0.057
102
BRN028 Brain Cancer 70 0.057
103
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.057
104
c GST048 Gastrointestinal System Benign Neoplasm 38 0.057
105
BND014 Bone Development Disease 40 0.057
106
ACR002 Acrocapitofemoral Dysplasia 33 0.057
107
P PLY019 Polyneuropathy 56 0.056
108
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.056
109
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.056
110
P NRV007 Nervous System Disease 71 0.056
111
P GRV001 Graves' Disease 59 0.055
112
PRP030 Purpura 58 0.055
113
ART016 Aortic Aneurysm 69 0.055
114
PLY020 Polyradiculoneuropathy 45 0.054
115
SFT003 Soft Tissue Sarcoma 57 0.052
116
c CRN214 Coronary Heart Disease 5 22 0.051
117
P HML002 Hemolytic Anemia 62 0.051
118
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 42 0.050
119
ADP007 Adie Pupil 34 0.049
120
PTT009 Pituitary Gland Disease 47 0.049
121
P CRB042 Cerebellar Ataxia 63 0.049
122
ETN001 Eating Disorder 58 0.049
123
ACR007 Acromegaly 66 0.049
124
c MLG068 Malignant Glioma 51 0.049
125
MST016 Mesothelioma, Somatic 51 0.048
126
CMR002 Coumarin Resistance 48 0.048
127
HYP085 Hypothalamic Disease 44 0.047
128
c DLT002 Dilated Cardiomyopathy 76 0.046
129
P MTR004 Maturity-Onset Diabetes of the Young 58 0.046
130
WLL006 Wells Syndrome 59 0.046
131
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.045
132
P ECL001 Eclampsia 54 0.045
133
P CHR345 Chronic Pain 50 0.045
134
KLN001 Klinefelter's Syndrome 50 0.045
135
GDS001 Good Syndrome 44 0.044
136
MSC004 Muscle Tissue Disease 34 0.044
137
VTM003 Vitamin Metabolic Disorder 30 0.044
138
MRB003 Morbid Obesity 58 0.042
139
c XRD019 Xeroderma Pigmentosum, Group C 52 0.042
140
SXL003 Sexual Disorder 42 0.042
141
SPN369 Spinal Disease 39 0.042
142
c CRN173 Coronary Heart Disease 8 18 0.042
143
c PRC016 Pre-Eclampsia 56 0.042
144
P ATM019 Autoimmune Polyendocrine Syndrome 43 0.042
145
P HNT016 Huntington Disease 80 0.042
146
SXD001 Sex Differentiation Disease 38 0.042
147
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.042
148
ATX038 Ataxia and Polyneuropathy, Adult-Onset 21 0.042
149
EXF001 Exfoliation Syndrome 57 0.041
150
SML020 Small Patella Syndrome 36 0.041
151
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 18 0.041
152
DBT087 Diabetes Insipidus, Neurohypophyseal 58 0.040
153
P PLN008 Peeling Skin Syndrome 45 0.040
154
VSC047 Vascular Malformation 45 0.040
155
P ATX024 Ataxia-Oculomotor Apraxia 3 31 0.040
156
VSC007 Vascular Disease 67 0.039
157
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.039
158
VSC009 Vascular Skin Disease 19 0.039
159
P BPL003 Bipolar Disorder 62 0.037
160
P THY097 Thyroid Hormone Resistance 54 0.037
161
c PLN021 Peeling Skin Syndrome 3 29 0.037
162
CHN016 Cohen Syndrome 54 0.035
163
c HYP355 Hypothyroidism, Congenital, Nongoitrous, 3 25 0.035
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