Search results for cirrhosis due to liver phosphorylase kinase deficiency

89 hits were found for cirrhosis due to liver phosphorylase kinase deficiency

# Family MCID Name MIFTS Score
1
P HPT021 Hepatitis 75 0.896
2
P LVR013 Liver Disease 76 0.700
3
LVR012 Liver Cirrhosis 73 0.699
4
c BLD140 Blood Group, I System 37 0.605
5
END072 Endotheliitis 46 0.588
6
P HPT023 Hepatocellular Carcinoma 94 0.570
7
P BRS047 Breast Cancer 100 0.471
8
P LKM002 Leukemia 75 0.460
9
P LYM118 Lymphoma 71 0.432
10
P PNC044 Pancreatitis 64 0.420
11
P CLR023 Colorectal Cancer 98 0.419
12
P ADN016 Adenocarcinoma 71 0.418
13
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.406
14
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.382
15
P LNG032 Lung Cancer 99 0.359
16
PRS047 Prostatitis 59 0.340
17
NRN002 Neuronitis 43 0.331
18
P THY032 Thyroiditis 56 0.313
19
AGN016 Aging 65 0.312
20
MLN008 Melanoma 72 0.305
21
GST053 Gastric Cancer 84 0.292
22
P ART022 Arthritis 77 0.285
23
CRB009 Cerebritis 41 0.280
24
PHS018 Phosphorylase Kinase Deficiency 37 0.279
25
P ESP024 Esophagitis 64 0.272
26
SQM006 Squamous Cell Carcinoma 74 0.269
27
c SML038 Small Cell Cancer of the Lung 67 0.255
28
SRC014 Sarcoma 68 0.244
29
HYP266 Hypoxia 61 0.243
30
P CRV039 Cervicitis 49 0.240
31
P MYP004 Myopathy 69 0.238
32
P HML002 Hemolytic Anemia 62 0.228
33
P RHM011 Rheumatoid Arthritis 91 0.227
34
P NRP001 Neuropathy 63 0.223
35
P MYC084 Mycobacterium Tuberculosis 1 69 0.220
36
P PNM007 Pneumonia 70 0.220
37
P MYC007 Myocardial Infarction 81 0.219
38
ADN018 Adenoma 63 0.214
39
CYS001 Cystic Fibrosis 85 0.205
40
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.196
41
CHL065 Cholangiocarcinoma 70 0.194
42
P GLY013 Glycogen Storage Disease 61 0.190
43
P GLM007 Glomerulonephritis 61 0.189
44
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.185
45
c VRL010 Viral Hepatitis 59 0.179
46
P ANR048 Aniridia 1 68 0.178
47
ANR038 Anorexia Nervosa 1 21 0.174
48
BLD137 Blood Group--Ahonen 17 0.173
49
P RNG031 Ring Chromosome Y Syndrome 29 0.172
50
P BCL006 B-Cell Lymphomas 70 0.171
51
PRP030 Purpura 61 0.166
52
P PSR002 Psoriasis 65 0.156
53
HMT018 Hematopoietic Stem Cell Transplantation 58 0.150
54
ART140 Arteries, Anomalies of 51 0.149
55
P CRN018 Coronary Artery Anomaly 69 0.148
56
HYP066 Hyperglycemia 64 0.147
57
HPT082 Hepatic Adenomas, Familial 52 0.145
58
ALR002 Al-Raqad Syndrome 30 0.145
59
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.145
60
c ACT075 Acute Myocardial Infarction 64 0.142
61
P DRR001 Diarrhea 60 0.142
62
P PRD008 Periodontitis 67 0.135
63
SPS057 Spasticity 41 0.130
64
ALP072 Alpha-Fetoprotein Deficiency 32 0.129
65
LYM133 Lymphoma, Hodgkin, Classic 78 0.129
66
P HYP061 Hypertrophic Cardiomyopathy 65 0.126
67
INT079 Intrahepatic Cholangiocarcinoma 60 0.126
68
PST011 Pustulosis of Palm and Sole 47 0.123
69
NSP002 Nasopharyngitis 46 0.122
70
P NTR004 Neutropenia 60 0.120
71
ESP021 Esophageal Cancer 79 0.120
72
SCH014 Schistosomiasis 62 0.118
73
P HYP265 Hypotonia 40 0.117
74
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.115
75
P FNC004 Fanconi Syndrome 54 0.114
76
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.113
77
CMM004 Common Variable Immunodeficiency 71 0.112
78
ALP046 Alport Syndrome, X-Linked 74 0.107
79
MNT001 Mantle Cell Lymphoma 76 0.107
80
LSH001 Leishmaniasis 71 0.106
81
c GLY007 Glycogen Storage Disease Iv 51 0.102
82
THR004 Thrombocytosis 55 0.100
83
PLY150 Polykaryocytosis Inducer 20 0.099
84
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.098
85
BLD163 Blood Group, Dombrock System 23 0.096
86
P KLZ004 Kala-Azar 1 31 0.091
87
LYM027 Lymphopenia 56 0.087
88
ADP007 Adie Pupil 41 0.068
89
c GLY044 Glycogen Storage Disease Ixc 30 0.064
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