Search results for CPT

85 hits were found for CPT

# Family MCID Name MIFTS Score
1
CRN295 Carnitine Palmitoyltransferase I Deficiency 46 8.095
2
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 55 6.478
3
CRN302 Carnitine Palmitoyltransferase Ii Deficiency, Lethal Neonatal 28 4.926
4
CRN294 Carnitine Palmitoyltransferase Ii Deficiency, Myopathic, Stress-Induced 24 4.202
5
CRN057 Carnitine Palmitoyltransferase I Deficiency , Muscle 12 2.474
6
c BLD140 Blood Group, I System 37 0.277
7
PST028 Post-Traumatic Stress Disorder 59 0.173
8
PSY004 Psychotic Disorder 72 0.163
9
MNT002 Mental Depression 60 0.100
10
P HPT021 Hepatitis 75 0.082
11
ANX010 Anxiety 72 0.082
12
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.082
13
P PRS038 Personality Disorder 65 0.082
14
ALC007 Alcohol Dependence 65 0.082
15
P ENC018 Encephalopathy 58 0.082
16
BRN022 Bronchiectasis 55 0.082
17
P BRS047 Breast Cancer 100 0.058
18
P LNG032 Lung Cancer 99 0.058
19
P CLR023 Colorectal Cancer 98 0.058
20
P PNC035 Pancreatic Cancer 89 0.058
21
P PRS040 Prostate Cancer 88 0.058
22
CYS001 Cystic Fibrosis 85 0.058
23
P OVR042 Ovarian Cancer 82 0.058
24
ESP021 Esophageal Cancer 79 0.058
25
END057 Endometrial Cancer 76 0.058
26
P LVR013 Liver Disease 76 0.058
27
SQM006 Squamous Cell Carcinoma 74 0.058
28
LVR012 Liver Cirrhosis 73 0.058
29
THY028 Thyroid Cancer 72 0.058
30
MLN008 Melanoma 72 0.058
31
VSC007 Vascular Disease 71 0.058
32
P LYM118 Lymphoma 71 0.058
33
P SCH015 Schizophrenia 71 0.058
34
P ADN016 Adenocarcinoma 71 0.058
35
WRN001 Werner Syndrome 70 0.058
36
LNG099 Lung Disease 67 0.058
37
P CNJ013 Conjunctivitis 67 0.058
38
P ENC004 Encephalitis 66 0.058
39
GST050 Gastrointestinal System Disease 66 0.058
40
ACQ007 Acquired Immunodeficiency Syndrome 65 0.058
41
AGN016 Aging 65 0.058
42
VRC005 Varicose Veins 64 0.058
43
RSP006 Respiratory System Disease 63 0.058
44
SKN019 Skin Melanoma 63 0.058
45
P CTS001 Cutis Laxa 62 0.058
46
P HYP086 Hypothyroidism 62 0.058
47
P AGN002 Agnosia 61 0.058
48
P BPL003 Bipolar Disorder 61 0.058
49
STT001 Status Epilepticus 60 0.058
50
P PRT013 Portal Hypertension 59 0.058
51
HPT019 Hepatic Encephalopathy 59 0.058
52
PNC034 Pancreas Disease 59 0.058
53
PPL022 Papilloma 58 0.058
54
BRN038 Bronchial Disease 58 0.058
55
LYM019 Lymphosarcoma 58 0.058
56
ESP023 Esophageal Disease 58 0.058
57
P SBS003 Substance Abuse 57 0.058
58
IMM136 Immune System Disease 57 0.058
59
BNF002 Bone Fracture 56 0.058
60
BRN071 Brain Injury 54 0.058
61
TRM010 Traumatic Brain Injury 54 0.058
62
c OVR114 Ovarian Cancer 1 54 0.058
63
ALL009 Allergic Conjunctivitis 53 0.058
64
HPT009 Hepatopulmonary Syndrome 53 0.058
65
THY030 Thyroid Gland Disease 51 0.058
66
UTR033 Uterine Corpus Cancer 51 0.058
67
BRD004 Borderline Personality Disorder 50 0.058
68
HYP063 Hypersplenism 49 0.058
69
HPT014 Hepatorenal Syndrome 49 0.058
70
PRP036 Peripheral T-Cell Lymphoma 48 0.058
71
P CMP008 Compartment Syndrome 48 0.058
72
CHR008 Choroiditis 47 0.058
73
PPL058 Papilloma of Choroid Plexus 47 0.058
74
ESP002 Esophageal Varix 46 0.058
75
ESP027 Esophagus Squamous Cell Carcinoma 45 0.058
76
LYM024 Lymphatic System Disease 45 0.058
77
ESP025 Esophagus Adenocarcinoma 42 0.058
78
P PSD086 Pseudoarthrosis 41 0.058
79
P DYS005 Dyslexia 39 0.058
80
P MYG005 Myoglobinuria 37 0.058
81
ATY002 Atypical Choroid Plexus Papilloma 37 0.058
82
SCH011 Schizotypal Personality Disorder 36 0.058
83
c MYG004 Myoglobinuria, Acute Recurrent, Autosomal Recessive 33 0.058
84
P RNG031 Ring Chromosome Y Syndrome 29 0.058
85
c CNG120 Congenital Pseudoarthrosis 15 0.058
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