Search results for "cirrhosis due to liver phosphorylase kinase deficiency"

The MalaCard for "cirrhosis due to liver phosphorylase kinase deficiency" has been retired.
Searching MalaCards for entries containing "cirrhosis due to liver phosphorylase kinase deficiency"

74 hits were found for 'cirrhosis due to liver phosphorylase kinase deficiency'

# Family MCID Name MIFTS Score
1
P HPT021 Hepatitis 74 0.858
2
P LVR013 Liver Disease 76 0.632
3
LVR012 Liver Cirrhosis 71 0.629
4
END072 Endotheliitis 41 0.605
5
HPT023 Hepatocellular Carcinoma 90 0.583
6
P LKM002 Leukemia 70 0.477
7
P BRS047 Breast Cancer 100 0.467
8
P LYM118 Lymphoma 68 0.436
9
P PNC044 Pancreatitis 62 0.419
10
P CLR023 Colorectal Cancer 96 0.416
11
P ADN016 Adenocarcinoma 69 0.386
12
P LNG032 Lung Cancer 92 0.361
13
PRS047 Prostatitis 56 0.355
14
NRN002 Neuronitis 40 0.353
15
P OBS005 Obesity 91 0.334
16
P THY032 Thyroiditis 57 0.329
17
MLN008 Melanoma 61 0.312
18
PHS018 Phosphorylase Kinase Deficiency 33 0.297
19
GST053 Gastric Cancer 52 0.295
20
CRB009 Cerebritis 36 0.285
21
P ART022 Arthritis 73 0.282
22
P ESP024 Esophagitis 62 0.270
23
P MYP004 Myopathy 67 0.270
24
c VRL010 Viral Hepatitis 60 0.256
25
P CRD011 Cardiomyopathy 66 0.249
26
P HML002 Hemolytic Anemia 60 0.245
27
HYP266 Hypoxia 55 0.245
28
SRC014 Sarcoma 66 0.244
29
TBR010 Tuberculosis 70 0.235
30
P RHM011 Rheumatoid Arthritis 87 0.234
31
P RNL014 Renal Cell Carcinoma 80 0.231
32
P MYC007 Myocardial Infarction 80 0.226
33
P PNM007 Pneumonia 67 0.225
34
P GLY013 Glycogen Storage Disease 58 0.225
35
P NRP001 Neuropathy 57 0.219
36
ADN018 Adenoma 59 0.214
37
ALR002 Al-Raqad Syndrome 36 0.213
38
CYS001 Cystic Fibrosis 87 0.202
39
P LYM026 Lymphoblastic Leukemia 60 0.198
40
P THR014 Thrombocytopenia 63 0.194
41
P GLM007 Glomerulonephritis 56 0.187
42
P BCL006 B-Cell Lymphomas 64 0.177
43
PCK002 Pick Disease 66 0.176
44
P PSR002 Psoriasis 63 0.172
45
HYP066 Hyperglycemia 61 0.148
46
P CRN211 Coronary Artery Disease 74 0.147
47
P TCL004 T-Cell Leukemia 44 0.146
48
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.145
49
P DRR001 Diarrhea 60 0.145
50
ART111 Artery Disease 56 0.143
51
P HYP061 Hypertrophic Cardiomyopathy 64 0.140
52
HMT018 Hematopoietic Stem Cell Transplantation 39 0.137
53
P OST012 Osteoarthritis 81 0.136
54
P PRD008 Periodontitis 46 0.133
55
SPS057 Spasticity 41 0.132
56
HDG012 Hodgkin Lymphoma 75 0.131
57
c ACT073 Acute Leukemia 61 0.130
58
P NTR004 Neutropenia 59 0.128
59
ESP021 Esophageal Cancer 75 0.126
60
NSP002 Nasopharyngitis 39 0.122
61
P STM004 Stomach Cancer 73 0.119
62
GST071 Gastrointestinal Carcinoma 37 0.119
63
P LRY019 Laryngitis 55 0.117
64
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.112
65
P FNC004 Fanconi Syndrome 54 0.111
66
MNT001 Mantle Cell Lymphoma 72 0.110
67
SCH014 Schistosomiasis 59 0.109
68
P TRM003 Tremor 54 0.106
69
CHR008 Choroiditis 43 0.106
70
P GCH001 Gaucher's Disease 63 0.100
71
CMM004 Common Variable Immunodeficiency 68 0.100
72
P DYS021 Dysautonomia 47 0.095
73
CNT098 Central Core Disease 68 0.086
74
LYM027 Lymphopenia 54 0.075