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"

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

# Family MCID Name MIFTS Score
1
P HPT021 Hepatitis 69 0.777
2
LVR012 Liver Cirrhosis 67 0.602
3
P LVR013 Liver Disease 75 0.564
4
P HPT023 Hepatocellular Carcinoma 92 0.528
5
END072 Endotheliitis 42 0.517
6
P BRS047 Breast Cancer 100 0.401
7
P LKM002 Leukemia 71 0.394
8
P LYM118 Lymphoma 69 0.369
9
P CLR023 Colorectal Cancer 97 0.367
10
P PNC044 Pancreatitis 61 0.363
11
P ADN016 Adenocarcinoma 69 0.343
12
P LNG032 Lung Cancer 95 0.308
13
PRS047 Prostatitis 56 0.295
14
NRN002 Neuronitis 41 0.286
15
P THY032 Thyroiditis 54 0.274
16
MLN008 Melanoma 62 0.264
17
GST053 Gastric Cancer 78 0.262
18
PHS018 Phosphorylase Kinase Deficiency 34 0.258
19
P ART022 Arthritis 75 0.256
20
CRB009 Cerebritis 39 0.245
21
P ESP024 Esophagitis 61 0.245
22
c VRL010 Viral Hepatitis 60 0.241
23
SQM006 Squamous Cell Carcinoma 70 0.240
24
P MYP004 Myopathy 67 0.235
25
P CRD011 Cardiomyopathy 68 0.217
26
P CRV039 Cervicitis 45 0.213
27
SRC014 Sarcoma 66 0.210
28
HYP266 Hypoxia 56 0.210
29
TBR010 Tuberculosis 70 0.208
30
P HML002 Hemolytic Anemia 62 0.206
31
RTN023 Retinitis 50 0.205
32
P RNL014 Renal Cell Carcinoma 82 0.203
33
P RHM011 Rheumatoid Arthritis 89 0.203
34
P PNM007 Pneumonia 68 0.196
35
P MYC007 Myocardial Infarction 79 0.195
36
P NRP001 Neuropathy 59 0.194
37
ADN018 Adenoma 58 0.189
38
P GLY013 Glycogen Storage Disease 60 0.181
39
CYS001 Cystic Fibrosis 83 0.178
40
P GLM007 Glomerulonephritis 59 0.166
41
ALR002 Al-Raqad Syndrome 36 0.157
42
P BCL006 B-Cell Lymphomas 65 0.151
43
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.148
44
PRP030 Purpura 58 0.147
45
P PSR002 Psoriasis 61 0.140
46
P CRN211 Coronary Artery Disease 74 0.130
47
HYP066 Hyperglycemia 61 0.130
48
ART111 Artery Disease 55 0.128
49
P DRR001 Diarrhea 60 0.128
50
P PRD008 Periodontitis 63 0.126
51
HMT018 Hematopoietic Stem Cell Transplantation 41 0.125
52
P TCL004 T-Cell Leukemia 47 0.124
53
P ART023 Arthropathy 64 0.123
54
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.123
55
SPS057 Spasticity 42 0.119
56
BNC003 Bone Cancer 58 0.117
57
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.116
58
P HYP069 Hyperparathyroidism 58 0.116
59
HDG012 Hodgkin Lymphoma 77 0.113
60
GST071 Gastrointestinal Carcinoma 42 0.112
61
ESP021 Esophageal Cancer 76 0.109
62
INT079 Intrahepatic Cholangiocarcinoma 56 0.109
63
P NTR004 Neutropenia 59 0.108
64
HPT074 Hepatic Adenoma, Somatic 50 0.107
65
HYP037 Hyperhomocysteinemia 50 0.107
66
NSP002 Nasopharyngitis 40 0.106
67
CRR007 Cirrhosis, Cryptogenic 43 0.105
68
P HYP265 Hypotonia 38 0.101
69
P FNC004 Fanconi Syndrome 49 0.100
70
SCH014 Schistosomiasis 58 0.098
71
AND005 Androgen Insensitivity Syndrome, Mild 16 0.098
72
MNT001 Mantle Cell Lymphoma 72 0.097
73
HNM002 Hinman Syndrome 25 0.094
74
c ADL017 Adult T-Cell Leukemia 60 0.094
75
CMM004 Common Variable Immunodeficiency 68 0.091
76
CNT098 Central Core Disease 65 0.085
77
PRD007 Periodontal Disease 60 0.081
78
LYM027 Lymphopenia 56 0.076
79
SYN007 Synovitis 58 0.074
80
MYC006 Mycosis Fungoides 66 0.064
81
c GLY044 Glycogen Storage Disease Ixc 28 0.063
82
PRS037 Periostitis 30 0.058
83
RNL011 Renal Osteodystrophy 45 0.055