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