Search results for "hepatocellular carcinoma, childhood-onset"

The MalaCard for "hepatocellular carcinoma, childhood-onset" has been retired.
Searching MalaCards for entries containing "hepatocellular carcinoma, childhood-onset"

111 hits were found for 'hepatocellular carcinoma, childhood-onset'

# Family MCID Name MIFTS Score
1
CHL128 Childhood Hepatocellular Carcinoma 30 5.875
2
END072 Endotheliitis 41 0.310
3
P PNC044 Pancreatitis 62 0.226
4
P LPS004 Lupus Erythematosus 63 0.156
5
ACD009 Acid-Labile Subunit, Deficiency of 37 0.145
6
ALR002 Al-Raqad Syndrome 36 0.139
7
P OBS005 Obesity 91 0.129
8
PCK002 Pick Disease 66 0.124
9
NRN002 Neuronitis 40 0.123
10
HPT074 Hepatic Adenoma, Somatic 35 0.119
11
P PRP029 Porphyria 56 0.116
12
CRB009 Cerebritis 36 0.116
13
GRW007 Growth Hormone Deficiency 49 0.116
14
INS024 Insulin-Like Growth Factor I 75 0.110
15
c THR092 Thrombophilia Due to Thrombin Defect 56 0.108
16
P ATX004 Ataxia 53 0.106
17
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.104
18
P KDN018 Kidney Disease 64 0.101
19
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.092
20
NTR005 Nutritional Deficiency Disease 51 0.092
21
P PLY041 Polymyositis 49 0.090
22
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.089
23
P ART022 Arthritis 73 0.089
24
ALN001 Aland Island Eye Disease 45 0.089
25
ISC004 Ischemia 56 0.088
26
VSC011 Vasculitis 62 0.087
27
FML039 Female Reproductive System Disease 49 0.086
28
P ENC018 Encephalopathy 59 0.086
29
P PRP003 Porphyria Cutanea Tarda 63 0.085
30
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.085
31
P OVR049 Ovarian Disease 54 0.084
32
P PRS038 Personality Disorder 60 0.084
33
P SPS003 Spastic Diplegia 49 0.082
34
SKN023 Skin Tag 48 0.081
35
c TRC078 Trichohepatoenteric Syndrome 2 30 0.081
36
PRP027 Peripheral Vascular Disease 69 0.080
37
HYP056 Hypoglycemia 60 0.080
38
P ALC004 Alcohol Abuse 57 0.080
39
ANR040 Aneurysm 56 0.078
40
SPC003 Specific Developmental Disorder 39 0.078
41
P NRV007 Nervous System Disease 71 0.077
42
P PLY019 Polyneuropathy 53 0.076
43
ACR041 Acromelic Frontonasal Dysostosis 45 0.076
44
BRT030 Birth Defects 44 0.076
45
P RHM011 Rheumatoid Arthritis 87 0.076
46
c ACT027 Acute Pancreatitis 59 0.076
47
P GLM007 Glomerulonephritis 56 0.075
48
PTY003 Pityriasis Rubra Pilaris 46 0.074
49
MVM001 Movement Disease 45 0.071
50
P MYS005 Myositis 57 0.071
51
CNN005 Connective Tissue Disease 60 0.071
52
PRP030 Purpura 60 0.070
53
CMR002 Coumarin Resistance 49 0.068
54
KWS002 Kawasaki Disease 70 0.068
55
P PSR002 Psoriasis 63 0.068
56
LRN003 Learning Disability 49 0.067
57
c CNG401 Congenital Heart Disease 67 0.067
58
P RSP003 Respiratory Failure 68 0.066
59
PLY020 Polyradiculoneuropathy 42 0.065
60
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.065
61
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.065
62
P CRB042 Cerebellar Ataxia 64 0.064
63
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 41 0.064
64
ETN001 Eating Disorder 59 0.063
65
RHM027 Rheumatic Disease 55 0.063
66
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.062
67
ART016 Aortic Aneurysm 67 0.062
68
ADM013 Adamantinoma of Long Bones 57 0.061
69
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.060
70
RSP006 Respiratory System Disease 61 0.060
71
OVR063 Overnutrition 49 0.058
72
P ECL001 Eclampsia 55 0.058
73
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.058
74
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 19 0.058
75
PRP016 Paraplegia 49 0.058
76
ACR002 Acrocapitofemoral Dysplasia 35 0.057
77
BND014 Bone Development Disease 40 0.057
78
SPC010 Speech and Communication Disorders 42 0.057
79
P HML002 Hemolytic Anemia 60 0.056
80
P CRD011 Cardiomyopathy 66 0.055
81
P MTR004 Maturity-Onset Diabetes of the Young 58 0.054
82
BLM002 Bulimia Nervosa 54 0.053
83
P HRT032 Heart Disease 64 0.052
84
PRP019 Peripheral Nervous System Disease 52 0.052
85
c CRN214 Coronary Heart Disease 5 22 0.052
86
SXL003 Sexual Disorder 45 0.051
87
c XRD019 Xeroderma Pigmentosum, Group C 46 0.051
88
P ATM019 Autoimmune Polyendocrine Syndrome 43 0.051
89
P THR015 Thrombophilia 59 0.050
90
PRT011 Protein C Deficiency 52 0.050
91
SML020 Small Patella Syndrome 36 0.049
92
MRB003 Morbid Obesity 59 0.049
93
c PRC016 Pre-Eclampsia 57 0.049
94
c DLT002 Dilated Cardiomyopathy 75 0.048
95
P PRN026 Porencephaly 47 0.048
96
WLL006 Wells Syndrome 57 0.047
97
GDS001 Good Syndrome 46 0.047
98
P CHR345 Chronic Pain 45 0.046
99
P HMF004 Hemifacial Spasm 38 0.046
100
VTM003 Vitamin Metabolic Disorder 31 0.045
101
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.043
102
P CLL015 Collagen Disease 49 0.043
103
c CRN173 Coronary Heart Disease 8 19 0.043
104
MRC001 Marchiafava Bignami Disease 33 0.042
105
EXF001 Exfoliation Syndrome 56 0.041
106
P PLN008 Peeling Skin Syndrome 45 0.041
107
VSC009 Vascular Skin Disease 21 0.041
108
P BPL003 Bipolar Disorder 58 0.040
109
c PLN021 Peeling Skin Syndrome 3 30 0.038
110
CHN016 Cohen Syndrome 55 0.036
111
VSC007 Vascular Disease 51 0.036