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 29 5.864
2
END072 Endotheliitis 42 0.311
3
P PNC044 Pancreatitis 60 0.225
4
P LPS004 Lupus Erythematosus 63 0.156
5
ACD009 Acid-Labile Subunit, Deficiency of 48 0.137
6
P OBS005 Obesity 93 0.126
7
GRW007 Growth Hormone Deficiency 48 0.117
8
P PRP029 Porphyria 58 0.116
9
NRN002 Neuronitis 42 0.108
10
INS024 Insulin-Like Growth Factor I 74 0.106
11
c THR092 Thrombophilia Due to Thrombin Defect 56 0.106
12
ALR002 Al-Raqad Syndrome 36 0.106
13
P ATX004 Ataxia 53 0.102
14
CRB009 Cerebritis 38 0.100
15
HPT074 Hepatic Adenoma, Somatic 51 0.092
16
NTR005 Nutritional Deficiency Disease 39 0.089
17
P ART022 Arthritis 75 0.088
18
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.084
19
P OVR049 Ovarian Disease 55 0.084
20
ALN001 Aland Island Eye Disease 45 0.083
21
P PRP003 Porphyria Cutanea Tarda 64 0.083
22
P SPS003 Spastic Diplegia 53 0.082
23
PRP027 Peripheral Vascular Disease 69 0.082
24
ISC004 Ischemia 59 0.082
25
c TRC078 Trichohepatoenteric Syndrome 2 31 0.081
26
ACR041 Acromelic Frontonasal Dysostosis 46 0.081
27
BRT030 Birth Defects 43 0.081
28
P PLY041 Polymyositis 51 0.080
29
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.079
30
HYP056 Hypoglycemia 61 0.079
31
FML039 Female Reproductive System Disease 48 0.079
32
SPC003 Specific Developmental Disorder 40 0.079
33
P ENC018 Encephalopathy 59 0.077
34
LRN003 Learning Disability 51 0.075
35
P PRS038 Personality Disorder 61 0.072
36
P RHM011 Rheumatoid Arthritis 88 0.072
37
PTY003 Pityriasis Rubra Pilaris 46 0.067
38
ANR040 Aneurysm 57 0.067
39
CNN005 Connective Tissue Disease 61 0.066
40
P PLY017 Polyarteritis Nodosa 55 0.066
41
VSC011 Vasculitis 62 0.065
42
HNM002 Hinman Syndrome 25 0.065
43
c ACT027 Acute Pancreatitis 56 0.065
44
KWS002 Kawasaki Disease 70 0.065
45
P MYS005 Myositis 56 0.064
46
P GLM007 Glomerulonephritis 56 0.064
47
P NRV007 Nervous System Disease 71 0.064
48
P PLY019 Polyneuropathy 54 0.064
49
P PSR002 Psoriasis 63 0.063
50
P HRT032 Heart Disease 76 0.063
51
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.062
52
PRP030 Purpura 59 0.062
53
ETN001 Eating Disorder 60 0.060
54
P CRD011 Cardiomyopathy 67 0.060
55
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.059
56
BND014 Bone Development Disease 42 0.058
57
ACR002 Acrocapitofemoral Dysplasia 36 0.058
58
SPC010 Speech and Communication Disorders 46 0.058
59
PLY020 Polyradiculoneuropathy 44 0.055
60
P TRN020 Turner Syndrome 64 0.055
61
ART016 Aortic Aneurysm 67 0.055
62
OVR063 Overnutrition 49 0.054
63
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 42 0.054
64
ADP007 Adie Pupil 34 0.054
65
c CRN214 Coronary Heart Disease 5 23 0.053
66
P HML002 Hemolytic Anemia 60 0.051
67
PRP016 Paraplegia 49 0.051
68
RSP006 Respiratory System Disease 62 0.050
69
VSC007 Vascular Disease 67 0.050
70
P CRB042 Cerebellar Ataxia 64 0.050
71
CMR002 Coumarin Resistance 48 0.048
72
SXL003 Sexual Disorder 47 0.048
73
SPN369 Spinal Disease 41 0.047
74
P MTR004 Maturity-Onset Diabetes of the Young 57 0.047
75
P ECL001 Eclampsia 54 0.047
76
c DLT002 Dilated Cardiomyopathy 75 0.047
77
WLL006 Wells Syndrome 56 0.046
78
GDS001 Good Syndrome 45 0.046
79
P CHR345 Chronic Pain 49 0.046
80
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.045
81
MSC004 Muscle Tissue Disease 36 0.045
82
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.045
83
P ATM019 Autoimmune Polyendocrine Syndrome 42 0.045
84
VTM003 Vitamin Metabolic Disorder 33 0.045
85
MRB003 Morbid Obesity 58 0.045
86
CHR001 Churg-Strauss Syndrome 49 0.045
87
MRC001 Marchiafava Bignami Disease 50 0.044
88
VSC047 Vascular Malformation 45 0.044
89
c CRN173 Coronary Heart Disease 8 20 0.044
90
STR067 Stroke, Ischemic 77 0.043
91
P THR015 Thrombophilia 59 0.043
92
BLM002 Bulimia Nervosa 54 0.043
93
c XRD019 Xeroderma Pigmentosum, Group C 47 0.043
94
SCR035 Sacral Agenesis with Vertebral Anomalies 33 0.043
95
EXF001 Exfoliation Syndrome 57 0.041
96
PRT011 Protein C Deficiency 51 0.041
97
P PLN008 Peeling Skin Syndrome 47 0.041
98
BRN045 Brunner Syndrome 42 0.041
99
SML020 Small Patella Syndrome 36 0.041
100
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 18 0.041
101
P BPL003 Bipolar Disorder 62 0.040
102
P PRN026 Porencephaly 47 0.040
103
MGL016 Megaloblastic Anemia-1, Finnish Type 46 0.040
104
c MYT012 Myotonia Congenita, Recessive 42 0.040
105
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.040
106
P ATX024 Ataxia-Oculomotor Apraxia 3 31 0.040
107
VSC009 Vascular Skin Disease 22 0.040
108
P HMF004 Hemifacial Spasm 39 0.038
109
c PLN021 Peeling Skin Syndrome 3 31 0.038
110
CHN016 Cohen Syndrome 55 0.037
111
HMD003 Hemidystonia 28 0.037