Search results for CPT

96 hits were found for CPT

# Family MCID Name MIFTS Score
1
CPT003 Cpt Deficiency, Hepatic, Type Ia 40 7.128
2
CRN183 Carnitine Palmitoyltransferase Ii Deficiency 54 4.837
3
CPT005 Cpt Ii Deficiency, Lethal Neonatal 25 4.757
4
CPT004 Cpt Deficiency, Hepatic, Type Ii 39 4.133
5
MYP007 Myopathy Due to Cpt Ii Deficiency 26 4.133
6
CRN057 Carnitine Palmitoyltransferase I Deficiency , Muscle 10 2.400
7
PST028 Post-Traumatic Stress Disorder 57 0.148
8
ACT084 Acute Stress Disorder 40 0.148
9
PSY004 Psychotic Disorder 67 0.125
10
DSS008 Disease of Mental Health 52 0.125
11
P HPT021 Hepatitis 69 0.112
12
P ALC004 Alcohol Abuse 59 0.097
13
SBS003 Substance Abuse 54 0.097
14
CND002 Conduct Disorder 54 0.097
15
LRN003 Learning Disability 49 0.097
16
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.079
17
ALC007 Alcohol Dependence 63 0.079
18
P PRS038 Personality Disorder 62 0.079
19
HYP056 Hypoglycemia 61 0.079
20
P ENC018 Encephalopathy 59 0.079
21
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.079
22
DRG003 Drug Dependence 50 0.079
23
SBS004 Substance Dependence 47 0.079
24
SXL003 Sexual Disorder 42 0.079
25
ALR002 Al-Raqad Syndrome 36 0.079
26
P MYG005 Myoglobinuria 35 0.079
27
P SCH015 Schizophrenia 77 0.056
28
c DLT002 Dilated Cardiomyopathy 76 0.056
29
P LVR013 Liver Disease 75 0.056
30
P PLM036 Pulmonary Fibrosis 71 0.056
31
CRZ001 Crouzon Syndrome 70 0.056
32
c HYP595 Hypertension, Essential 69 0.056
33
P CRD011 Cardiomyopathy 68 0.056
34
ANX002 Anxiety Disorder 67 0.056
35
WRN001 Werner Syndrome 67 0.056
36
LVR012 Liver Cirrhosis 67 0.056
37
P MYP004 Myopathy 67 0.056
38
P CNJ013 Conjunctivitis 64 0.056
39
P ENC004 Encephalitis 63 0.056
40
P BPL003 Bipolar Disorder 62 0.056
41
P PRT013 Portal Hypertension 60 0.056
42
STT001 Status Epilepticus 59 0.056
43
P CTS001 Cutis Laxa 58 0.056
44
LPD008 Lipid Metabolism Disorder 58 0.056
45
RSP006 Respiratory System Disease 58 0.056
46
P AGN002 Agnosia 57 0.056
47
GST050 Gastrointestinal System Disease 56 0.056
48
HPT019 Hepatic Encephalopathy 56 0.056
49
PRP019 Peripheral Nervous System Disease 55 0.056
50
PPL022 Papilloma 55 0.056
51
CHR029 Choroid Plexus Papilloma 55 0.056
52
ESP023 Esophageal Disease 54 0.056
53
SLP005 Sleep Disorder 53 0.056
54
END040 Endogenous Depression 53 0.056
55
MNT002 Mental Depression 53 0.056
56
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.056
57
TRM010 Traumatic Brain Injury 52 0.056
58
BRN071 Brain Injury 52 0.056
59
BRN038 Bronchial Disease 51 0.056
60
DRG011 Drug Addiction 51 0.056
61
ALL009 Allergic Conjunctivitis 51 0.056
62
STM006 Stomach Disease 50 0.056
63
BRN022 Bronchiectasis 50 0.056
64
THR013 Thoracic Outlet Syndrome 50 0.056
65
CSY001 C Syndrome 50 0.056
66
HYP063 Hypersplenism 48 0.056
67
ATN002 Autonomic Nervous System Disease 48 0.056
68
P CMP008 Compartment Syndrome 48 0.056
69
HPT009 Hepatopulmonary Syndrome 48 0.056
70
VND001 Vein Disease 47 0.056
71
BRD004 Borderline Personality Disorder 47 0.056
72
GNG011 Gingival Disease 46 0.056
73
HPT014 Hepatorenal Syndrome 46 0.056
74
SPL012 Splenic Disease 46 0.056
75
HDN002 Head Injury 45 0.056
76
CHR008 Choroiditis 44 0.056
77
PHY002 Physical Disorder 43 0.056
78
HPT020 Hepatic Vascular Disease 42 0.056
79
SPC010 Speech and Communication Disorders 41 0.056
80
AYM001 Ayme-Gripp Syndrome 41 0.056
81
ESP002 Esophageal Varix 41 0.056
82
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.056
83
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.056
84
ATY002 Atypical Choroid Plexus Papilloma 38 0.056
85
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.056
86
SXD001 Sex Differentiation Disease 38 0.056
87
DRG001 Drug Psychosis 38 0.056
88
P DYS005 Dyslexia 37 0.056
89
TTR016 Tetra-Amelia Syndrome 36 0.056
90
c MLT010 Multiple Personality Disorder 36 0.056
91
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 33 0.056
92
SCH011 Schizotypal Personality Disorder 33 0.056
93
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 30 0.056
94
c MYG004 Myoglobinuria, Acute Recurrent, Autosomal Recessive 27 0.056
95
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.056
96
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.056
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