Search results for Citrulline

218 hits were found for Citrulline

# Family MCID Name MIFTS Score
1
CTR030 Citrulline Transport Defect 9 4.395
2
CTR172 Citrullinemia, Classic 58 2.683
3
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 58 2.560
4
URC002 Urea Cycle Disorder 50 2.511
5
P ART022 Arthritis 77 0.599
6
P RHM011 Rheumatoid Arthritis 91 0.577
7
LNG099 Lung Disease 67 0.168
8
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.145
9
P SHR001 Short Bowel Syndrome 52 0.145
10
VSC007 Vascular Disease 71 0.133
11
c BLD140 Blood Group, I System 37 0.133
12
P PLM037 Pulmonary Hypertension 79 0.126
13
SCK005 Sickle Cell Disease 54 0.126
14
SCK003 Sickle Cell Anemia 73 0.119
15
P MYP004 Myopathy 69 0.119
16
NRM005 Neuromuscular Disease 60 0.119
17
MSC033 Muscle Disorders 53 0.119
18
HMG005 Hemoglobinopathy 53 0.119
19
ART140 Arteries, Anomalies of 51 0.119
20
PLN005 Palindromic Rheumatism 46 0.119
21
MSC004 Muscle Tissue Disease 39 0.119
22
ATR076 Atrophic Muscular Disease 6 0.119
23
P MLT020 Multiple Sclerosis 85 0.111
24
P HRT032 Heart Disease 80 0.111
25
BRC012 Brucellosis 71 0.111
26
P ART023 Arthropathy 68 0.111
27
MSC157 Muscular Dystrophy, Duchenne Type 74 0.103
28
P ADL010 Adult Respiratory Distress Syndrome 67 0.103
29
P MSC005 Muscular Dystrophy 66 0.103
30
ISC004 Ischemia 66 0.103
31
MSC152 Muscular Dystrophy, Becker Type 64 0.103
32
RSP006 Respiratory System Disease 63 0.103
33
c ACT210 Acute Respiratory Distress Syndrome 63 0.103
34
P ART021 Arteriosclerosis 62 0.103
35
c CRD187 Cardiomyopathy, Dilated, 3b 46 0.103
36
MSC012 Muscular Dystrophy, Duchenne and Becker Type 35 0.103
37
c MYT029 Myotonia Congenita, Autosomal Recessive 32 0.103
38
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.103
39
P HPT021 Hepatitis 75 0.094
40
CNN005 Connective Tissue Disease 65 0.094
41
SYN007 Synovitis 61 0.094
42
P CRN300 Coronary Heart Disease 1 57 0.094
43
NWB001 Newborn Respiratory Distress Syndrome 56 0.094
44
RSP007 Respiratory Distress Syndrome, Infant 28 0.094
45
INS024 Insulin-Like Growth Factor I 83 0.084
46
ISC006 Ischemic Heart Disease 73 0.084
47
P FML018 Familial Mediterranean Fever 73 0.084
48
PRP027 Peripheral Vascular Disease 71 0.084
49
P CRN018 Coronary Artery Anomaly 69 0.084
50
P PRD008 Periodontitis 67 0.084
51
ATM095 Autoimmune Disease 66 0.084
52
P INT068 Intestinal Disease 65 0.084
53
HYP266 Hypoxia 61 0.084
54
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 55 0.084
55
PRP080 Peripheral Artery Disease 54 0.084
56
HRT038 Heart, Malformation of 22 0.084
57
P ALZ034 Alzheimer Disease 95 0.073
58
c SYS001 Systemic Lupus Erythematosus 86 0.073
59
AST005 Asthma 83 0.073
60
c HPT001 Hepatitis C 73 0.073
61
P DBT009 Diabetes Mellitus 72 0.073
62
P LPS004 Lupus Erythematosus 69 0.073
63
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.073
64
PSR001 Psoriatic Arthritis 66 0.073
65
GST050 Gastrointestinal System Disease 66 0.073
66
GST045 Gastroenteritis 65 0.073
67
INT066 Interstitial Lung Disease 63 0.073
68
RHM027 Rheumatic Disease 62 0.073
69
INT002 Intermittent Claudication 61 0.073
70
P VNT002 Ventricular Septal Defect 59 0.073
71
P ATR001 Atrioventricular Septal Defect 56 0.073
72
LYS003 Lysinuric Protein Intolerance 53 0.073
73
ESN011 Eisenmenger Syndrome 49 0.073
74
PLC008 Placenta Disease 48 0.073
75
END072 Endotheliitis 46 0.073
76
P ATR010 Atrial Heart Septal Defect 45 0.073
77
HRT011 Heart Septal Defect 44 0.073
78
SCR011 Scrapie 40 0.073
79
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 31 0.073
80
CMP035 Complete Atrioventricular Canal 27 0.073
81
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.059
82
P MYC007 Myocardial Infarction 81 0.059
83
CRH001 Crohn's Disease 80 0.059
84
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.059
85
c HPT073 Hepatitis C Virus 73 0.059
86
P GRF003 Graft-Versus-Host Disease 72 0.059
87
c SPN225 Spondyloarthropathy 1 71 0.059
88
WRN001 Werner Syndrome 70 0.059
89
P CLC063 Celiac Disease 1 65 0.059
90
c PRC016 Pre-Eclampsia 65 0.059
91
PRD007 Periodontal Disease 64 0.059
92
PLM031 Poliomyelitis 64 0.059
93
P PNC044 Pancreatitis 64 0.059
94
MCS002 Mucositis 61 0.059
95
BRN056 Bronchopulmonary Dysplasia 61 0.059
96
JNT002 Joint Disorders 60 0.059
97
P SJG008 Sjogren Syndrome 58 0.059
98
P ECL001 Eclampsia 57 0.059
99
IMM136 Immune System Disease 57 0.059
100
SPN051 Spondylitis 55 0.059
101
c INF071 Inflammatory Bowel Disease 1 54 0.059
102
SPN041 Spinal Cord Disease 54 0.059
103
P CLL015 Collagen Disease 53 0.059
104
PRT038 Protein-Energy Malnutrition 52 0.059
105
ILT001 Ileitis 52 0.059
106
CRB186 Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to 52 0.059
107
P INF037 Inflammatory Bowel Disease 52 0.059
108
MYL001 Myelitis 52 0.059
109
ACT017 Acute Chest Syndrome 50 0.059
110
ANX004 Anoxia 49 0.059
111
MTC069 Mitochondrial Disorders 49 0.059
112
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.059
113
BRN080 Brain Ischemia 45 0.059
114
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 43 0.059
115
NRN002 Neuronitis 43 0.059
116
P PRC031 Preeclampsia/eclampsia 1 41 0.059
117
PST020 Postpoliomyelitis Syndrome 39 0.059
118
GLC008 Glucose Metabolism Disease 38 0.059
119
ENT004 Enthesopathy 38 0.059
120
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 34 0.059
121
INF009 Inflammatory Spondylopathy 32 0.059
122
ATM052 Autoimmune Disease 1 30 0.059
123
P BRS047 Breast Cancer 100 0.042
124
P LNG032 Lung Cancer 99 0.042
125
P PRS040 Prostate Cancer 88 0.042
126
OST012 Osteoarthritis 88 0.042
127
ULC004 Ulcerative Colitis 80 0.042
128
P BLD134 Bladder Cancer 78 0.042
129
P LVR013 Liver Disease 76 0.042
130
P NRV007 Nervous System Disease 75 0.042
131
P OST002 Osteoporosis 75 0.042
132
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.042
133
PHN003 Phenylketonuria 73 0.042
134
c JVN010 Juvenile Rheumatoid Arthritis 71 0.042
135
P EPL164 Epilepsy 70 0.042
136
c HPT016 Hepatitis B 68 0.042
137
P ORT004 Orthostatic Intolerance 68 0.042
138
LGH007 Leigh Syndrome 68 0.042
139
P HYD006 Hydrocephalus 68 0.042
140
P TMP003 Temporal Arteritis 67 0.042
141
c MLG068 Malignant Glioma 66 0.042
142
MXD005 Mixed Connective Tissue Disease 66 0.042
143
VSC011 Vasculitis 66 0.042
144
ACQ007 Acquired Immunodeficiency Syndrome 65 0.042
145
P DRM010 Dermatomyositis 65 0.042
146
MLT157 Multiple System Atrophy 1 65 0.042
147
P PSR002 Psoriasis 65 0.042
148
AGN016 Aging 65 0.042
149
CRT072 Creutzfeldt-Jakob Disease 65 0.042
150
P MYS005 Myositis 63 0.042
151
CLT003 Colitis 63 0.042
152
GST033 Gestational Diabetes 62 0.042
153
FTT001 Fatty Liver Disease 62 0.042
154
P GLM045 Glioma 61 0.042
155
P CTR002 Cataract 60 0.042
156
c SCL052 Scleroderma, Familial Progressive 60 0.042
157
P DRR001 Diarrhea 60 0.042
158
PRS047 Prostatitis 59 0.042
159
P ENC018 Encephalopathy 58 0.042
160
MCR088 Microscopic Polyangiitis 58 0.042
161
PPL022 Papilloma 58 0.042
162
BRN038 Bronchial Disease 58 0.042
163
ARG002 Argininosuccinic Aciduria 57 0.042
164
GST023 Gastric Ulcer 57 0.042
165
BRN106 Burns 57 0.042
166
PRN019 Perinatal Necrotizing Enterocolitis 56 0.042
167
HPT046 Hepatic Veno-Occlusive Disease 56 0.042
168
P MSC003 Muscular Atrophy 55 0.042
169
P INT070 Intestinal Obstruction 55 0.042
170
c MCR113 Microvascular Complications of Diabetes 3 55 0.042
171
SPS003 Spastic Diplegia 55 0.042
172
ENT011 Enterocolitis 52 0.042
173
ATN002 Autonomic Nervous System Disease 51 0.042
174
ATN005 Autonomic Dysfunction 51 0.042
175
PRN023 Prion Disease 51 0.042
176
RYS001 Reye Syndrome 50 0.042
177
CRY004 Cryoglobulinemia 49 0.042
178
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.042
179
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.042
180
P CMP008 Compartment Syndrome 48 0.042
181
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 47 0.042
182
PST011 Pustulosis of Palm and Sole 47 0.042
183
MLT016 Multicentric Reticulohistiocytosis 47 0.042
184
P DYS021 Dysautonomia 47 0.042
185
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.042
186
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.042
187
ANT039 Antisynthetase Syndrome 46 0.042
188
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.042
189
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.042
190
SYS003 Systolic Heart Failure 44 0.042
191
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.042
192
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.042
193
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.042
194
c MCR130 Microvascular Complications of Diabetes 6 42 0.042
195
RHM014 Rheumatoid Vasculitis 40 0.042
196
HPT004 Hepatic Coma 40 0.042
197
c PSR017 Psoriasis 2 40 0.042
198
c PSR018 Psoriasis 13 39 0.042
199
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.042
200
AMN002 Amino Acid Metabolic Disorder 38 0.042
201
PYR037 Pyruvate Carboxylase Deficiency 38 0.042
202
TRP004 Tropical Sprue 38 0.042
203
c PSR028 Psoriasis 7 37 0.042
204
NCT003 N-Acetylglutamate Synthase Deficiency 36 0.042
205
c PSR032 Psoriasis 11 35 0.042
206
P CTR177 Citrullinemia, Type Ii, Adult-Onset 34 0.042
207
c MCR120 Microvascular Complications of Diabetes 7 34 0.042
208
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.042
209
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.042
210
c MCR133 Microvascular Complications of Diabetes 4 32 0.042
211
c SPS158 Spastic Paraplegia 9a, Autosomal Dominant 31 0.042
212
RFL002 Reflex Epilepsy 27 0.042
213
PHS029 Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic 23 0.042
214
HML018 Homologous Wasting Disease 18 0.042
215
INB001 Inborn Amino Acid Metabolism Disorder 16 0.042
216
ACT228 Acute Radiation Syndrome 16 0.042
217
GRN020 Granulomatous Hypophysitis 15 0.042
218
AMN012 Aminoacidopathies 15 0.042
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