Search results for Citrulline

215 hits were found for Citrulline

# Family MCID Name MIFTS Score
1
CTR030 Citrulline Transport Defect 9 4.395
2
CTR172 Citrullinemia, Classic 55 2.560
3
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 58 2.537
4
URC002 Urea Cycle Disorder 50 2.510
5
P ART022 Arthritis 76 0.698
6
P RHM011 Rheumatoid Arthritis 80 0.677
7
LNG099 Lung Disease 67 0.189
8
P PLM037 Pulmonary Hypertension 75 0.152
9
P SHR001 Short Bowel Syndrome 51 0.146
10
VSC007 Vascular Disease 68 0.126
11
P ART023 Arthropathy 67 0.126
12
SCK005 Sickle Cell Disease 54 0.126
13
SCK003 Sickle Cell Anemia 72 0.119
14
P MYP004 Myopathy 68 0.119
15
ART140 Arteries, Anomalies of 65 0.119
16
NRM005 Neuromuscular Disease 60 0.119
17
HMG005 Hemoglobinopathy 53 0.119
18
P MSC033 Muscle Disorders 52 0.119
19
PLN005 Palindromic Rheumatism 46 0.119
20
MSC004 Muscle Tissue Disease 39 0.119
21
ATR076 Atrophic Muscular Disease 18 0.119
22
P MLT020 Multiple Sclerosis 78 0.112
23
P HPT021 Hepatitis 76 0.112
24
BRC012 Brucellosis 70 0.112
25
CNN005 Connective Tissue Disease 64 0.112
26
HYP266 Hypoxia 61 0.112
27
MSC157 Muscular Dystrophy, Duchenne Type 68 0.103
28
P MSC005 Muscular Dystrophy 66 0.103
29
P ADL010 Adult Respiratory Distress Syndrome 66 0.103
30
ISC004 Ischemia 65 0.103
31
ATM095 Autoimmune Disease 64 0.103
32
RSP006 Respiratory System Disease 63 0.103
33
c ACT210 Acute Respiratory Distress Syndrome 61 0.103
34
P ART021 Arteriosclerosis 60 0.103
35
MSC152 Muscular Dystrophy, Becker Type 60 0.103
36
c CRD187 Cardiomyopathy, Dilated, 3b 46 0.103
37
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.103
38
MSC012 Muscular Dystrophy, Duchenne and Becker Type 36 0.103
39
c SYS001 Systemic Lupus Erythematosus 86 0.094
40
AST005 Asthma 82 0.094
41
P HRT032 Heart Disease 74 0.094
42
c HPT001 Hepatitis C 71 0.094
43
P LPS004 Lupus Erythematosus 68 0.094
44
P PRD008 Periodontitis 66 0.094
45
PSR001 Psoriatic Arthritis 65 0.094
46
c CRN300 Coronary Heart Disease 1 64 0.094
47
RHM027 Rheumatic Disease 62 0.094
48
BRN056 Bronchopulmonary Dysplasia 60 0.094
49
SYN007 Synovitis 60 0.094
50
NWB001 Newborn Respiratory Distress Syndrome 52 0.094
51
ENT004 Enthesopathy 46 0.094
52
RSP007 Respiratory Distress Syndrome, Infant 34 0.094
53
P ALZ034 Alzheimer Disease 87 0.084
54
INS024 Insulin-Like Growth Factor I 82 0.084
55
P FML018 Familial Mediterranean Fever 73 0.084
56
ISC006 Ischemic Heart Disease 72 0.084
57
PRP027 Peripheral Vascular Disease 70 0.084
58
P CRN018 Coronary Artery Anomaly 68 0.084
59
P INT068 Intestinal Disease 64 0.084
60
P DBT009 Diabetes Mellitus 64 0.084
61
INT066 Interstitial Lung Disease 62 0.084
62
INT002 Intermittent Claudication 61 0.084
63
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.084
64
JNT002 Joint Disorders 59 0.084
65
TYP041 Type I 56 0.084
66
IMM136 Immune System Disease 56 0.084
67
PRP080 Peripheral Artery Disease 53 0.084
68
P CLL015 Collagen Disease 52 0.084
69
ANX004 Anoxia 49 0.084
70
END072 Endotheliitis 45 0.084
71
HRT038 Heart, Malformation of 32 0.084
72
CRH001 Crohn's Disease 78 0.073
73
PLM129 Pulmonary Disease, Chronic Obstructive 72 0.073
74
c HPT073 Hepatitis C Virus 72 0.073
75
c PLM164 Pulmonary Hypertension, Primary, 1 66 0.073
76
GST050 Gastrointestinal System Disease 64 0.073
77
GST045 Gastroenteritis 64 0.073
78
P MYS005 Myositis 63 0.073
79
PLC008 Placenta Disease 61 0.073
80
P VNT002 Ventricular Septal Defect 58 0.073
81
P ATR001 Atrioventricular Septal Defect 56 0.073
82
P SJG008 Sjogren Syndrome 54 0.073
83
P ATR010 Atrial Heart Septal Defect 54 0.073
84
LYS003 Lysinuric Protein Intolerance 52 0.073
85
ESN011 Eisenmenger Syndrome 50 0.073
86
HRT011 Heart Septal Defect 43 0.073
87
NRN002 Neuronitis 41 0.073
88
SCR011 Scrapie 40 0.073
89
CMP035 Complete Atrioventricular Canal 30 0.073
90
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 29 0.073
91
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.060
92
P MYC007 Myocardial Infarction 79 0.060
93
P LVR013 Liver Disease 75 0.060
94
ULC004 Ulcerative Colitis 72 0.060
95
P GRF003 Graft-Versus-Host Disease 71 0.060
96
P CLC063 Celiac Disease 1 71 0.060
97
c SPN225 Spondyloarthropathy 1 71 0.060
98
WRN001 Werner Syndrome 69 0.060
99
PRD007 Periodontal Disease 64 0.060
100
P PNC044 Pancreatitis 64 0.060
101
INC002 Inclusion Body Myositis 63 0.060
102
CLT003 Colitis 62 0.060
103
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.060
104
FTT001 Fatty Liver Disease 60 0.060
105
MCS002 Mucositis 60 0.060
106
P INF032 Infertility 59 0.060
107
c PRC016 Pre-Eclampsia 59 0.060
108
PLM031 Poliomyelitis 58 0.060
109
P ECL001 Eclampsia 57 0.060
110
ILT001 Ileitis 56 0.060
111
SPN051 Spondylitis 55 0.060
112
c INF071 Inflammatory Bowel Disease 1 53 0.060
113
CRB186 Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to 53 0.060
114
P INF037 Inflammatory Bowel Disease 53 0.060
115
GLC008 Glucose Metabolism Disease 52 0.060
116
MYL001 Myelitis 51 0.060
117
PRT038 Protein-Energy Malnutrition 51 0.060
118
SPN041 Spinal Cord Disease 51 0.060
119
P NNL004 Nonalcoholic Fatty Liver Disease 51 0.060
120
ACT017 Acute Chest Syndrome 49 0.060
121
IDP024 Idiopathic Inflammatory Myopathy 49 0.060
122
P MTC069 Mitochondrial Disorders 49 0.060
123
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.060
124
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 47 0.060
125
BRN080 Brain Ischemia 44 0.060
126
PST020 Postpoliomyelitis Syndrome 41 0.060
127
c PRC031 Preeclampsia/eclampsia 1 39 0.060
128
ALL014 Allergic Encephalomyelitis 36 0.060
129
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 34 0.060
130
ATM052 Autoimmune Disease 1 34 0.060
131
P BRS047 Breast Cancer 100 0.042
132
P LNG032 Lung Cancer 98 0.042
133
P PRS040 Prostate Cancer 90 0.042
134
MYL069 Myeloma, Multiple 83 0.042
135
OST012 Osteoarthritis 82 0.042
136
P OST002 Osteoporosis 76 0.042
137
MLT157 Multiple System Atrophy 1 73 0.042
138
P NRV007 Nervous System Disease 73 0.042
139
PHN003 Phenylketonuria 73 0.042
140
c JVN010 Juvenile Rheumatoid Arthritis 69 0.042
141
P BLD134 Bladder Cancer 69 0.042
142
P EPL164 Epilepsy 69 0.042
143
P HYD006 Hydrocephalus 69 0.042
144
P ORT004 Orthostatic Intolerance 68 0.042
145
LGH007 Leigh Syndrome 67 0.042
146
c HPT016 Hepatitis B 67 0.042
147
P TMP003 Temporal Arteritis 66 0.042
148
P PSR002 Psoriasis 65 0.042
149
CRT072 Creutzfeldt-Jakob Disease 65 0.042
150
MXD005 Mixed Connective Tissue Disease 65 0.042
151
VSC011 Vasculitis 65 0.042
152
TTN003 Tetanus 64 0.042
153
AGN016 Aging 64 0.042
154
c SCL052 Scleroderma, Familial Progressive 64 0.042
155
P DRM010 Dermatomyositis 64 0.042
156
ACQ007 Acquired Immunodeficiency Syndrome 63 0.042
157
P ENC018 Encephalopathy 62 0.042
158
SCH014 Schistosomiasis 62 0.042
159
GST033 Gestational Diabetes 60 0.042
160
ANR040 Aneurysm 60 0.042
161
PRS047 Prostatitis 60 0.042
162
P SPN052 Spondyloarthropathy 60 0.042
163
P CTR002 Cataract 60 0.042
164
PPL022 Papilloma 58 0.042
165
MCR088 Microscopic Polyangiitis 57 0.042
166
HPT046 Hepatic Veno-Occlusive Disease 57 0.042
167
GST023 Gastric Ulcer 57 0.042
168
ARG002 Argininosuccinic Aciduria 57 0.042
169
BRN038 Bronchial Disease 56 0.042
170
P DRR001 Diarrhea 56 0.042
171
BRN106 Burns 56 0.042
172
PRN019 Perinatal Necrotizing Enterocolitis 56 0.042
173
P INT070 Intestinal Obstruction 56 0.042
174
P THY032 Thyroiditis 55 0.042
175
P MSC003 Muscular Atrophy 54 0.042
176
SPS003 Spastic Diplegia 54 0.042
177
P GLM045 Glioma 54 0.042
178
ENT011 Enterocolitis 54 0.042
179
c MCR113 Microvascular Complications of Diabetes 3 52 0.042
180
ATN002 Autonomic Nervous System Disease 51 0.042
181
ATN005 Autonomic Dysfunction 50 0.042
182
PRN023 Prion Disease 50 0.042
183
RYS001 Reye Syndrome 49 0.042
184
CRY004 Cryoglobulinemia 49 0.042
185
P CMP008 Compartment Syndrome 47 0.042
186
AMN002 Amino Acid Metabolic Disorder 47 0.042
187
MLT016 Multicentric Reticulohistiocytosis 47 0.042
188
SYS003 Systolic Heart Failure 46 0.042
189
ANT039 Antisynthetase Syndrome 46 0.042
190
SPN119 Spondylarthropathy 45 0.042
191
P DYS021 Dysautonomia 43 0.042
192
RHM014 Rheumatoid Vasculitis 41 0.042
193
CRB009 Cerebritis 41 0.042
194
c MCR130 Microvascular Complications of Diabetes 6 40 0.042
195
HPT004 Hepatic Coma 40 0.042
196
c PSR017 Psoriasis 2 39 0.042
197
c MLG068 Malignant Glioma 38 0.042
198
c PSR028 Psoriasis 7 38 0.042
199
c PSR032 Psoriasis 11 38 0.042
200
PYR037 Pyruvate Carboxylase Deficiency 38 0.042
201
TRP004 Tropical Sprue 37 0.042
202
c PSR018 Psoriasis 13 37 0.042
203
c MCR120 Microvascular Complications of Diabetes 7 37 0.042
204
NCT003 N-Acetylglutamate Synthase Deficiency 36 0.042
205
P CTR177 Citrullinemia, Type Ii, Adult-Onset 35 0.042
206
c MCR133 Microvascular Complications of Diabetes 4 35 0.042
207
c SPS158 Spastic Paraplegia 9a, Autosomal Dominant 32 0.042
208
RFL002 Reflex Epilepsy 27 0.042
209
AMN012 Aminoacidopathies 24 0.042
210
PHS029 Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic 19 0.042
211
HML018 Homologous Wasting Disease 18 0.042
212
ACT228 Acute Radiation Syndrome 17 0.042
213
INB001 Inborn Amino Acid Metabolism Disorder 16 0.042
214
MTC112 Mitochondrial Dna-Associated Leigh Syndrome 15 0.042
215
GRN020 Granulomatous Hypophysitis 15 0.042
Content
Loading form....