Search results for Citrulline

254 hits were found for Citrulline

# Family MCID Name MIFTS Score
1
CTR030 Citrulline Transport Defect 7 3.596
2
P CTR001 Citrullinemia 60 2.670
3
ORN006 Ornithine Transcarbamylase Deficiency 60 2.589
4
URC002 Urea Cycle Disorder 51 2.553
5
P ART022 Arthritis 72 0.567
6
P RHM011 Rheumatoid Arthritis 87 0.545
7
LNG099 Lung Disease 61 0.154
8
MTH009 Mouth Disease 62 0.149
9
P SHR001 Short Bowel Syndrome 47 0.138
10
MSC004 Muscle Tissue Disease 37 0.138
11
P MSC033 Muscle Disorders 52 0.132
12
BRT030 Birth Defects 44 0.132
13
P PLM037 Pulmonary Hypertension 77 0.119
14
VSC007 Vascular Disease 65 0.119
15
SCK003 Sickle Cell Anemia 71 0.112
16
P MYP004 Myopathy 68 0.112
17
RSP006 Respiratory System Disease 60 0.112
18
ART111 Artery Disease 55 0.112
19
NRM005 Neuromuscular Disease 55 0.112
20
c PND001 Pain Disorder 55 0.112
21
HMG005 Hemoglobinopathy 51 0.112
22
SCK005 Sickle Cell Disease 51 0.112
23
PLN005 Palindromic Rheumatism 42 0.112
24
P OBS005 Obesity 91 0.105
25
P ART023 Arthropathy 62 0.105
26
P ADL010 Adult Respiratory Distress Syndrome 60 0.105
27
CHL071 Child Syndrome 59 0.105
28
KDS001 Kid Syndrome 57 0.105
29
c ACT210 Acute Respiratory Distress Syndrome 56 0.105
30
AMN002 Amino Acid Metabolic Disorder 48 0.105
31
PHY002 Physical Disorder 43 0.105
32
DCH001 Duchenne Muscular Dystrophy 79 0.097
33
P HRT032 Heart Disease 75 0.097
34
BCK001 Becker Muscular Dystrophy 71 0.097
35
P MSC005 Muscular Dystrophy 65 0.097
36
ISC004 Ischemia 59 0.097
37
ART021 Arteriosclerosis 57 0.097
38
ADL002 Adult Syndrome 57 0.097
39
c PRG106 Progressive Muscular Dystrophy 40 0.097
40
c CRD187 Cardiomyopathy, Dilated, 3b 35 0.097
41
NLL002 Null Syndrome 26 0.097
42
MSC012 Muscular Dystrophy, Duchenne and Becker Type 25 0.097
43
ATR076 Atrophic Muscular Disease 18 0.097
44
INS024 Insulin-Like Growth Factor I 75 0.089
45
P HPT021 Hepatitis 68 0.089
46
P SHR029 Short Syndrome 61 0.089
47
CNN005 Connective Tissue Disease 61 0.089
48
P INT068 Intestinal Disease 59 0.089
49
NWB001 Newborn Respiratory Distress Syndrome 46 0.089
50
SYN007 Synovitis 41 0.089
51
RSP007 Respiratory Distress Syndrome, Infant 25 0.089
52
P CRN178 Coronary Heart Disease 6 22 0.089
53
c ADL080 Adult Acute Respiratory Distress Syndrome 22 0.089
54
c CRN174 Coronary Heart Disease 2 21 0.089
55
P CRN211 Coronary Artery Disease 73 0.080
56
TBR010 Tuberculosis 69 0.080
57
PRP027 Peripheral Vascular Disease 65 0.080
58
ATH003 Atherosclerosis 65 0.080
59
HYP266 Hypoxia 55 0.080
60
GST050 Gastrointestinal System Disease 53 0.080
61
ISC006 Ischemic Heart Disease 53 0.080
62
P PRD008 Periodontitis 46 0.080
63
PRP080 Peripheral Artery Disease 36 0.080
64
c SYS001 Systemic Lupus Erythematosus 86 0.069
65
P AST005 Asthma 81 0.069
66
P LPS004 Lupus Erythematosus 63 0.069
67
PSR001 Psoriatic Arthritis 63 0.069
68
c HPT001 Hepatitis C 62 0.069
69
BRC012 Brucellosis 61 0.069
70
P VNT002 Ventricular Septal Defect 58 0.069
71
WLL006 Wells Syndrome 58 0.069
72
GST045 Gastroenteritis 57 0.069
73
RHM027 Rheumatic Disease 57 0.069
74
c PRC016 Pre-Eclampsia 56 0.069
75
INT002 Intermittent Claudication 55 0.069
76
P PRC031 Preeclampsia/eclampsia 1 55 0.069
77
LYS003 Lysinuric Protein Intolerance 53 0.069
78
CSY001 C Syndrome 53 0.069
79
P ATR001 Atrioventricular Septal Defect 52 0.069
80
P ECL001 Eclampsia 51 0.069
81
DRG003 Drug Dependence 48 0.069
82
c SVR005 Severe Pre-Eclampsia 48 0.069
83
ATN002 Autonomic Nervous System Disease 48 0.069
84
ESN011 Eisenmenger Syndrome 46 0.069
85
GDS001 Good Syndrome 46 0.069
86
P ATR010 Atrial Heart Septal Defect 42 0.069
87
END072 Endotheliitis 41 0.069
88
HRT011 Heart Septal Defect 40 0.069
89
BLD054 Blood Protein Disease 39 0.069
90
SCR011 Scrapie 36 0.069
91
BNS002 Bone Structure Disease 36 0.069
92
PLC008 Placenta Disease 32 0.069
93
P ATR066 Atrial Septal Defect 2 31 0.069
94
c VNT028 Ventricular Septal Defect 1 29 0.069
95
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 27 0.069
96
c ATR062 Atrial Septal Defect 1 25 0.069
97
c ATR047 Atrioventricular Septal Defect 2 24 0.069
98
SNG003 Single Ventricular Heart 23 0.069
99
c VNT026 Ventricular Septal Defect 2 22 0.069
100
c ATR056 Atrial Septal Defect 9 21 0.069
101
c CRN175 Coronary Heart Disease 4 20 0.069
102
c PRC032 Preeclampsia/eclampsia 2 18 0.069
103
c PRC033 Preeclampsia/eclampsia 3 18 0.069
104
P MYC007 Myocardial Infarction 77 0.056
105
CRH001 Crohn's Disease 73 0.056
106
c HPT073 Hepatitis C Virus 70 0.056
107
P CLC005 Celiac Disease 69 0.056
108
WRN001 Werner Syndrome 68 0.056
109
RCT015 Reactive Arthritis 63 0.056
110
P INF037 Inflammatory Bowel Disease 62 0.056
111
P PNC044 Pancreatitis 60 0.056
112
INT066 Interstitial Lung Disease 57 0.056
113
P ORL007 Oral Cavity Cancer 57 0.056
114
ORL011 Oral Cancer 56 0.056
115
JNT002 Joint Disorders 55 0.056
116
P MTC069 Mitochondrial Disorders 55 0.056
117
PLM031 Poliomyelitis 55 0.056
118
IMM136 Immune System Disease 53 0.056
119
VSC006 Vascular Cancer 52 0.056
120
CRB152 Carbamoylphosphate Synthetase I Deficiency 51 0.056
121
BNM001 Bone Marrow Cancer 51 0.056
122
SPN051 Spondylitis 51 0.056
123
HPT046 Hepatic Veno-Occlusive Disease 50 0.056
124
P CLL015 Collagen Disease 50 0.056
125
P SJG001 Sjogren's Syndrome 49 0.056
126
MSS002 Mass Syndrome 49 0.056
127
PRT038 Protein-Energy Malnutrition 48 0.056
128
BRN056 Bronchopulmonary Dysplasia 48 0.056
129
MYL001 Myelitis 48 0.056
130
STM006 Stomach Disease 47 0.056
131
NTR005 Nutritional Deficiency Disease 47 0.056
132
SPN041 Spinal Cord Disease 46 0.056
133
ACT017 Acute Chest Syndrome 45 0.056
134
P PLM025 Pulmonary Venoocclusive Disease 44 0.056
135
GLC008 Glucose Metabolism Disease 44 0.056
136
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.056
137
ANX004 Anoxia 44 0.056
138
PRD007 Periodontal Disease 42 0.056
139
BNC003 Bone Cancer 42 0.056
140
CHR413 Chronic Myocardial Ischemia 41 0.056
141
BRN080 Brain Ischemia 40 0.056
142
c CHR096 Chronic Pulmonary Heart Disease 40 0.056
143
NRN002 Neuronitis 39 0.056
144
BND014 Bone Development Disease 39 0.056
145
ADJ001 Adjustment Disorder 38 0.056
146
P FML187 Familial Hypertension 37 0.056
147
ATM012 Autoimmune Disease of Blood 37 0.056
148
ORL003 Oral Tuberculosis 36 0.056
149
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 34 0.056
150
P ACT080 Acute Pulmonary Heart Disease 31 0.056
151
PST020 Postpoliomyelitis Syndrome 31 0.056
152
c PLM132 Pulmonary Venoocclusive Disease 2 30 0.056
153
c PLM128 Pulmonary Hypertension, Primary, 2 30 0.056
154
c PLM127 Pulmonary Hypertension, Primary, 3 29 0.056
155
c CNT068 Central Pain Syndrome 29 0.056
156
c MYC058 Myocardial Infarction 2 28 0.056
157
HST007 Histidine Metabolism Disease 28 0.056
158
PRM243 Primary Bone Cancer 25 0.056
159
c CRN172 Coronary Heart Disease 3 20 0.056
160
CRD217 Cardiac Tuberculosis 19 0.056
161
c CRN176 Coronary Heart Disease 9 18 0.056
162
ATM055 Autoimmune Disease 4 18 0.056
163
IDP075 Idiopathic and/or Familial Pulmonary Arterial Hypertension 13 0.056
164
SPN015 Spinal Polio 11 0.056
165
P BRS047 Breast Cancer 100 0.040
166
P LNG032 Lung Cancer 94 0.040
167
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.040
168
HV1006 Hiv-1 80 0.040
169
P OST012 Osteoarthritis 79 0.040
170
P LVR013 Liver Disease 72 0.040
171
PHN003 Phenylketonuria 72 0.040
172
ULC004 Ulcerative Colitis 72 0.040
173
P NRV007 Nervous System Disease 70 0.040
174
MLT021 Multiple System Atrophy 70 0.040
175
P LGH007 Leigh Syndrome 69 0.040
176
P RSP003 Respiratory Failure 68 0.040
177
P HYD006 Hydrocephalus 66 0.040
178
P EPL164 Epilepsy 65 0.040
179
P PSR002 Psoriasis 64 0.040
180
P OST002 Osteoporosis 63 0.040
181
c HPT016 Hepatitis B 62 0.040
182
VSC011 Vasculitis 62 0.040
183
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.040
184
CRT072 Creutzfeldt-Jakob Disease 62 0.040
185
MXD005 Mixed Connective Tissue Disease 61 0.040
186
ACQ007 Acquired Immunodeficiency Syndrome 60 0.040
187
P DRM010 Dermatomyositis 59 0.040
188
c MLG068 Malignant Glioma 59 0.040
189
P GLM045 Glioma 59 0.040
190
P DRR001 Diarrhea 59 0.040
191
FTT001 Fatty Liver Disease 59 0.040
192
ARG002 Argininosuccinic Aciduria 58 0.040
193
CLT003 Colitis 58 0.040
194
CTS003 Coats Disease 58 0.040
195
P CTR002 Cataract 57 0.040
196
ART017 Aortic Disease 57 0.040
197
P MYS005 Myositis 56 0.040
198
GST033 Gestational Diabetes 55 0.040
199
P INT070 Intestinal Obstruction 55 0.040
200
MCS002 Mucositis 54 0.040
201
PPL022 Papilloma 54 0.040
202
GST023 Gastric Ulcer 54 0.040
203
BRN038 Bronchial Disease 53 0.040
204
BRN106 Burns 52 0.040
205
MVM001 Movement Disease 52 0.040
206
MCR088 Microscopic Polyangiitis 51 0.040
207
RYS001 Reye Syndrome 50 0.040
208
P MSC003 Muscular Atrophy 49 0.040
209
P PLN008 Peeling Skin Syndrome 49 0.040
210
VND001 Vein Disease 49 0.040
211
P RNL015 Renal Hypertension 47 0.040
212
MLT016 Multicentric Reticulohistiocytosis 46 0.040
213
PRN023 Prion Disease 46 0.040
214
PRN019 Perinatal Necrotizing Enterocolitis 45 0.040
215
CRY004 Cryoglobulinemia 45 0.040
216
P CMP008 Compartment Syndrome 44 0.040
217
SYS003 Systolic Heart Failure 43 0.040
218
P HYP729 Hypersensitivity Reaction Disease 43 0.040
219
ANT039 Antisynthetase Syndrome 42 0.040
220
RHM014 Rheumatoid Vasculitis 41 0.040
221
CNV002 Conversion Disorder 40 0.040
222
MDY003 Mody, Type Ii 40 0.040
223
PYR037 Pyruvate Carboxylase Deficiency 39 0.040
224
GST078 Gastrointestinal Allergy 39 0.040
225
HPT004 Hepatic Coma 39 0.040
226
FNC002 Functional Diarrhea 39 0.040
227
HYP391 Hyperammonemia 38 0.040
228
c PLN017 Peeling Skin Syndrome 1 38 0.040
229
MTC005 Mitochondrial Metabolism Disease 38 0.040
230
GST007 Gastric Dilatation 37 0.040
231
NCT003 N-Acetylglutamate Synthase Deficiency 36 0.040
232
FNC006 Functional Gastric Disease 35 0.040
233
TRP004 Tropical Sprue 35 0.040
234
DDN007 Duodenal Disease 34 0.040
235
HGH001 High Pressure Neurological Syndrome 33 0.040
236
c AST037 Asthma 1 33 0.040
237
c DRR009 Diarrhea 6 33 0.040
238
c CTR142 Citrullinemia, Adult-Onset Type Ii 30 0.040
239
IMM076 Immunodeficiency 24 29 0.040
240
c SPS158 Spastic Paraplegia 9a, Autosomal Dominant 28 0.040
241
RFL002 Reflex Epilepsy 26 0.040
242
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.040
243
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 23 0.040
244
PHS020 Phosphoenolpyruvate Carboxykinase-1, Cytosolic, Deficiency 23 0.040
245
ACT228 Acute Radiation Syndrome 20 0.040
246
c INF083 Inflammatory Bowel Disease 24 20 0.040
247
c CLC038 Celiac Disease 10 18 0.040
248
PRP050 Peripheral Arterial Occlusive Disease 1 16 0.040
249
HML018 Homologous Wasting Disease 16 0.040
250
INB001 Inborn Amino Acid Metabolism Disorder 14 0.040
251
MTC024 Mitochondrial Genetic Disorders 14 0.040
252
GRN020 Granulomatous Hypophysitis 13 0.040
253
MNT045 Montefiore Syndrome 12 0.040
254
c SCN046 Secondary Short Bowel Syndrome 12 0.040
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