Search results for Citrulline

1172 hits were found for Citrulline

#	Family	MCID	Name	MIFTS	Score
1	P	RHM011	Rheumatoid Arthritis	82	38.610

2	P	ART022	Arthritis	71	30.841

3		CTR172	Citrullinemia, Classic	65	20.640

4		CTR030	Citrulline Transport Defect	9	18.733

5		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	16.340

6		ORN008	Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to	62	13.011

7		URC002	Urea Cycle Disorder	51	12.785

8		ATM095	Autoimmune Disease	61	12.301

9	P	PRD008	Periodontitis	64	10.855

10	P	SHR001	Short Bowel Syndrome	53	9.677

11		PLC002	Plica Syndrome	35	9.550

12		SYN007	Synovitis	55	9.550

13		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	8.808

14	P	PLM037	Pulmonary Hypertension	72	8.759

15		LNG099	Lung Disease	62	8.286

16		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	7.883

17		PSR001	Psoriatic Arthritis	62	7.750

18	c	JVN010	Juvenile Rheumatoid Arthritis	66	7.736

19		ENT004	Enthesopathy	51	7.701

20		INT066	Interstitial Lung Disease	60	6.623

21		CNN005	Connective Tissue Disease	67	6.204

22		CRH001	Crohn's Disease	80	6.083

23		SPN051	Spondylitis	51	6.053

24		INF009	Inflammatory Spondylopathy	30	6.053

25	c	SPN225	Spondyloarthropathy 1	70	5.982

26		PPL052	Papillomatosis, Confluent and Reticulated	34	5.973

27	P	LPS004	Lupus Erythematosus	61	5.680

28	P	VSC007	Vascular Disease	63	5.649

29	c	SYS001	Systemic Lupus Erythematosus	87	5.589

30	P	SCK005	Sickle Cell Disease	56	5.469

31		PLM129	Pulmonary Disease, Chronic Obstructive	74	5.469

32		MTC023	Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes	44	5.466

33		ENT011	Enterocolitis	55	5.379

34		48X005	48,xyyy	39	5.363

35	P	CTR177	Citrullinemia, Type Ii, Adult-Onset	55	5.332

36		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	62	5.281

37		LYS003	Lysinuric Protein Intolerance	57	5.238

38	P	ART023	Arthropathy	61	5.237

39		MCS002	Mucositis	56	5.196

40		PRN019	Perinatal Necrotizing Enterocolitis	60	5.152

41		TXC005	Toxic Shock Syndrome	62	5.081

42	c	SCL052	Scleroderma, Familial Progressive	61	5.034

43		ISC004	Ischemia	61	4.962

44	P	CTR077	Citrullinemia, Type Ii, Neonatal-Onset	41	4.933

45		HYP266	Hypoxia	57	4.932

46	P	INT068	Intestinal Disease	53	4.922

47	P	MLT020	Multiple Sclerosis	79	4.835

48	c	PRC016	Pre-Eclampsia	65	4.771

49	P	MSC005	Muscular Dystrophy	67	4.745

50	P	CLC063	Celiac Disease 1	66	4.662

51	P	HRT032	Heart Disease	81	4.647

52		SYS071	Systemic Autoimmune Disease	35	4.502

53		IMP005	Impotence	52	4.471

54	P	LCT001	Lactic Acidosis	51	4.436

55	P	VSC011	Vasculitis	61	4.429

56		47X002	47,xyy	48	4.405

57		CYT002	Cytokine Deficiency	43	4.377

58		HYP774	Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome	54	4.352

59	P	ADL010	Adult Respiratory Distress Syndrome	71	4.340

60	P	LVR013	Liver Disease	69	4.304

61	P	PRN023	Prion Disease	60	4.257

62	P	MTC069	Mitochondrial Disorders	57	4.237

63		FTT001	Fatty Liver Disease	62	4.204

64		ULC004	Ulcerative Colitis	74	4.199

65		BRN056	Bronchopulmonary Dysplasia	56	4.175

66	c	PRD040	Periodontitis, Chronic	52	4.165

67		ARG002	Argininosuccinic Aciduria	61	4.118

68		NNL005	Non-Alcoholic Fatty Liver Disease	63	4.075

69	P	INF037	Inflammatory Bowel Disease	53	4.070

70		ATH013	Atherosclerosis Susceptibility	63	4.043

71	P	SPN052	Spondyloarthropathy	55	4.002

72		ALL014	Allergic Encephalomyelitis	34	3.908

73	P	PLY041	Polymyositis	59	3.858

74		MTC004	Mitochondrial Encephalomyopathy	42	3.842

75		CHL068	Cholestasis	61	3.836

76		ART140	Arteries, Anomalies of	53	3.829

77	P	PLM036	Pulmonary Fibrosis	66	3.827

78		SCK003	Sickle Cell Anemia	74	3.822

79	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	3.807

80		DFC004	Deficiency Anemia	74	3.745

81		AGN016	Aging	54	3.728

82	c	TYP009	Type 2 Diabetes Mellitus	92	3.657

83	P	SJG008	Sjogren Syndrome	61	3.655

84		MSC157	Muscular Dystrophy, Duchenne Type	79	3.650

85	c	CHR684	Chronic Kidney Disease	69	3.634

86	c	HYP595	Hypertension, Essential	85	3.598

87	P	DRR001	Diarrhea	55	3.570

88	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	3.564

89		ANT039	Antisynthetase Syndrome	55	3.530

90	P	CRN300	Coronary Heart Disease 1	73	3.523

91		SCR011	Scrapie	39	3.505

92		OCL069	Ocular Motor Apraxia	57	3.503

93	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	3.451

94	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	3.451

95	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	3.451

96	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	3.451

97	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	3.451

98	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	3.451

99	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	3.451

100	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	3.451

101	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	3.451

102	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	3.451

103	P	ALZ034	Alzheimer Disease	87	3.450

104	P	ENC018	Encephalopathy	62	3.450

105		ACT228	Acute Radiation Syndrome	30	3.439

106		MTC005	Mitochondrial Metabolism Disease	45	3.394

107	P	SYS005	Systemic Scleroderma	74	3.376

108		PLN005	Palindromic Rheumatism	43	3.372

109		PRP027	Peripheral Vascular Disease	71	3.361

110	P	MYP004	Myopathy	67	3.343

111	P	DBT009	Diabetes Mellitus	67	3.339

112	c	HPT001	Hepatitis C	62	3.252

113		CRT072	Creutzfeldt-Jakob Disease	68	3.200

114		RCT015	Reactive Arthritis	61	3.183

115		CRH005	Crohn's Colitis	53	3.173

116	c	ACT027	Acute Pancreatitis	60	3.166

117		DMY004	Demyelinating Disease	50	3.166

118	P	GRF003	Graft-Versus-Host Disease	71	3.149

119		ATS010	Autosomal Recessive Disease	42	3.132

120	P	PSR002	Psoriasis	63	3.091

121		PST011	Pustulosis of Palm and Sole	52	3.091

122		LPP008	Lipoprotein Quantitative Trait Locus	65	3.088

123	c	ATM011	Autoimmune Hepatitis	63	3.080

124		PLM134	Pulmonary Fibrosis, Idiopathic	76	3.071

125		BNR002	Bone Resorption Disease	47	3.071

126	P	BRN022	Bronchiectasis	60	3.071

127		HTT002	Hutterite Cerebroosteonephrodysplasia Syndrome	25	3.036

128	P	MSC003	Muscular Atrophy	52	3.010

129	c	PLM164	Pulmonary Hypertension, Primary, 1	76	2.989

130	P	NTR004	Neutropenia	63	2.986

131	P	PNC044	Pancreatitis	61	2.986

132		TTN003	Tetanus	65	2.973

133	P	TMP003	Temporal Arteritis	69	2.934

134		MSC152	Muscular Dystrophy, Becker Type	69	2.927

135	P	AST005	Asthma	76	2.924

136		PRP080	Peripheral Artery Disease	54	2.900

137	P	MYS005	Myositis	56	2.898

138	P	ECL001	Eclampsia	52	2.892

139		CLT003	Colitis	63	2.861

140		TNS014	Tenosynovitis	46	2.860

141	c	HYP836	Hypercholesterolemia, Familial, 1	73	2.851

142		FLT011	Felty Syndrome	52	2.843

143		BRC012	Brucellosis	66	2.823

144	P	DRM010	Dermatomyositis	61	2.819

145		HPT004	Hepatic Coma	43	2.761

146		RYS001	Reye Syndrome	49	2.753

147		LVR012	Liver Cirrhosis	63	2.735

148	c	ACT135	Acute Graft Versus Host Disease	51	2.708

149		CRB186	Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to	50	2.698

150		NCT003	N-Acetylglutamate Synthase Deficiency	43	2.661

151		ARG007	Argininemia	58	2.660

152		URM002	Uremia	47	2.658

153		RPD005	Rapidly Involuting Congenital Hemangioma	46	2.651

154		BCT022	Bacterial Infectious Disease	56	2.621

155		PRT038	Protein-Energy Malnutrition	53	2.616

156		HYP066	Hyperglycemia	61	2.585

157		HPT019	Hepatic Encephalopathy	59	2.566

158	c	HPT073	Hepatitis C Virus	71	2.563

159	P	KLZ004	Kala-Azar 1	41	2.559

160		LSH001	Leishmaniasis	64	2.559

161		END086	End Stage Renal Disease	52	2.541

162	P	RSP003	Respiratory Failure	74	2.522

163	c	TYP008	Type 1 Diabetes Mellitus	70	2.512

164		OST012	Osteoarthritis	77	2.512

165		ORN004	Ornithinemia	13	2.497

166		SPN119	Spondylarthropathy	38	2.494

167		ESN011	Eisenmenger Syndrome	47	2.480

168	P	PLY187	Polyarticular Juvenile Idiopathic Arthritis	39	2.471

169	P	GLM007	Glomerulonephritis	60	2.471

170		ORT008	Orotic Aciduria	57	2.462

171		LPD008	Lipid Metabolism Disorder	62	2.462

172	P	FML018	Familial Mediterranean Fever	73	2.437

173	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	2.431

174	c	MGR028	Migraine with or Without Aura 1	64	2.431

175	P	LTR001	Lateral Sclerosis	58	2.431

176		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	2.425

177		CRB039	Cerebrovascular Disease	66	2.391

178	c	CHR464	Chronic Intestinal Failure	24	2.368

179		PRT251	Proteinuria, Chronic Benign	57	2.353

180	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	2.351

181		PPL022	Papilloma	53	2.349

182		SQM002	Squamous Cell Papilloma	46	2.349

183	P	MYC008	Myocarditis	59	2.349

184		PLM031	Poliomyelitis	63	2.326

185		PRT013	Portal Hypertension	59	2.315

186		GT001	Gout	64	2.307

187		MTB004	Metabolic Acidosis	48	2.276

188		MLR004	Malaria	80	2.276

189		SKN016	Skin Disease	63	2.274

190		MXD005	Mixed Connective Tissue Disease	57	2.274

191	P	TRN020	Turner Syndrome	67	2.269

192		TBL029	Tubulin, Beta	28	2.263

193	P	KDN018	Kidney Disease	72	2.263

194	P	ADN016	Adenocarcinoma	63	2.263

195		VSC003	Visceral Leishmaniasis	55	2.246

196	P	PRP019	Peripheral Nervous System Disease	58	2.246

197		PRM236	Primary Biliary Cholangitis	60	2.224

198	c	HPT016	Hepatitis B	62	2.219

199		BRN002	Bronchiolitis	57	2.173

200		ANX004	Anoxia	40	2.172

201		TRM010	Traumatic Brain Injury	51	2.172

202		HYP060	Hyperinsulinism	54	2.172

203		SPL018	Splenomegaly	49	2.172

204		ANC002	Anca-Associated Vasculitis	44	2.172

205		PYR037	Pyruvate Carboxylase Deficiency	45	2.171

206	P	CLR023	Colorectal Cancer	100	2.154

207	P	TRM003	Tremor	48	2.154

208		CNG034	Congestive Heart Failure	69	2.154

209		ADL002	Adult Syndrome	70	2.143

210		THR024	Thrombosis	56	2.128

211		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	2.124

212	c	MCR130	Microvascular Complications of Diabetes 6	41	2.124

213	c	MCR120	Microvascular Complications of Diabetes 7	47	2.124

214		CLR109	Colorectal Adenocarcinoma	50	2.124

215	c	MCR113	Microvascular Complications of Diabetes 3	52	2.124

216	c	MCR133	Microvascular Complications of Diabetes 4	41	2.124

217		SCH014	Schistosomiasis	56	2.124

218		BRN004	Brain Edema	54	2.111

219	c	DLT002	Dilated Cardiomyopathy	78	2.111

220	c	INH020	Inherited Metabolic Disorder	48	2.094

221		RCK004	Rickets	68	2.075

222	P	MNN013	Meningitis	65	2.075

223	P	HPT021	Hepatitis	69	2.072

224		OST159	Osteogenic Sarcoma	66	2.068

225		RNL114	Renal Cell Carcinoma, Nonpapillary	80	2.068

226	P	ANT006	Antiphospholipid Syndrome	55	2.068

227		DPR016	Depression	65	2.068

228		CVD001	Covid-19	57	2.066

229		LGH007	Leigh Syndrome	70	2.046

230		SPR126	Superior Semicircular Canal Dehiscence	41	2.026

231	c	HMG029	Hemoglobin Se Disease	40	2.026

232	c	ACT071	Acute Kidney Failure	60	2.023

233	c	RNG008	Ring Chromosome 13	30	2.023

234	c	LKM061	Leukemia, Acute Myeloid	83	2.023

235		PRT037	Pertussis	65	2.023

236		SVR004	Severe Combined Immunodeficiency	72	2.023

237		BRN071	Brain Injury	50	2.023

238	P	ATR001	Atrioventricular Septal Defect	55	1.979

239	P	VNT002	Ventricular Septal Defect	58	1.979

240		HRT011	Heart Septal Defect	49	1.979

241		END057	Endometrial Cancer	72	1.976

242		RHM033	Rheumatoid Factor-Positive Polyarticular Juvenile Idiopathic Arthritis	19	1.976

243		GLM045	Glioma	63	1.976

244		HLX001	Helix Syndrome	48	1.970

245		GNG013	Gingivitis	59	1.970

246	P	NRP001	Neuropathy	60	1.945

247	P	LPR021	Leprosy 3	71	1.939

248		HNS001	Hansen's Disease	32	1.939

249		ALL006	Allergic Asthma	56	1.929

250		GLL048	Glial Tumor	52	1.929

251	P	CRD119	Cardiac Arrest	67	1.929

252		HSH003	Hashimoto Thyroiditis	60	1.915

253	P	PNC035	Pancreatic Cancer	86	1.879

254	P	MLN008	Melanoma	76	1.879

255		CLN019	Colonic Disease	47	1.879

256		SPN035	Spindle Cell Sarcoma	54	1.857

257		TNS005	Tonsillitis	57	1.857

258		SRC014	Sarcoma	65	1.857

259	P	CRD246	Cardiovascular System Disease	56	1.854

260	c	ACT134	Acute Liver Failure	59	1.828

261	P	OST002	Osteoporosis	76	1.828

262	P	EXN002	Exanthem	58	1.828

263	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	1.828

264	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	1.828

265		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	66	1.828

266	P	OPN001	Open-Angle Glaucoma	55	1.828

267	P	HDC001	Headache	57	1.828

268		DWN001	Down Syndrome	70	1.815

269	c	CHL116	Cholestasis, Intrahepatic, of Pregnancy, 1	52	1.804

270	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	1.796

271		DHY010	Dihydrolipoamide Dehydrogenase Deficiency	47	1.796

272		PLM001	Pulmonary Tuberculosis	69	1.796

273		BNN003	Bone Inflammation Disease	48	1.796

274		ANK001	Ankylosis	51	1.796

275		MCR088	Microscopic Polyangiitis	51	1.796

276	P	LNG032	Lung Cancer	98	1.775

277		CLF027	Cleft Palate, Isolated	64	1.775

278	c	SML038	Small Cell Cancer of the Lung	69	1.775

279	c	GLC092	Glaucoma, Primary Open Angle	62	1.775

280		CLF001	Cleft Lip	53	1.775

281		FBR047	Fibromyalgia	58	1.775

282		CMB007	Combined Immunodeficiency	57	1.775

283		PRP030	Purpura	54	1.775

284		ACT017	Acute Chest Syndrome	50	1.765

285		INT002	Intermittent Claudication	61	1.759

286		ACR041	Acromelic Frontonasal Dysostosis	53	1.755

287		NWB001	Newborn Respiratory Distress Syndrome	56	1.755

288		CYS013	Cystinuria	66	1.750

289	P	AGG001	Aggressive Periodontitis	55	1.738

290	P	CTR002	Cataract	60	1.731

291	c	THR092	Thrombophilia Due to Thrombin Defect	74	1.719

292	P	ORF002	Orofacial Cleft	43	1.719

293	P	PRS040	Prostate Cancer	95	1.719

294	P	HPT023	Hepatocellular Carcinoma	96	1.719

295	P	MYC007	Myocardial Infarction	70	1.719

296		CLF056	Cleft Lip with or Without Cleft Palate	42	1.719

297	P	INT070	Intestinal Obstruction	57	1.719

298	P	DMN002	Dementia	66	1.719

299	P	UVT001	Uveitis	57	1.719

300		RYN005	Raynaud Phenomenon	45	1.719

301	P	PNM007	Pneumonia	67	1.686

302		SVR001	Severe Acute Respiratory Syndrome	67	1.665

303		IMM166	Immunodeficiency 27a	60	1.662

304		ISL109	Isolated Cleft Lip	33	1.661

305	P	LYM118	Lymphoma	67	1.661

306	P	SRC025	Sarcoidosis 1	71	1.661

307		ESP021	Esophageal Cancer	83	1.661

308		URT010	Ureteral Obstruction	45	1.661

309		ORF053	Orofacial Clefting Syndrome	31	1.661

310		INS001	Insulinoma	59	1.661

311		ADN018	Adenoma	59	1.661

312		ALL029	Allergic Disease	59	1.661

313		HGH043	High Grade Glioma	45	1.661

314		NNS002	Nonspecific Interstitial Pneumonia	42	1.661

315		GST045	Gastroenteritis	58	1.661

316	P	HYP265	Hypotonia	42	1.661

317	c	RNG015	Ring Chromosome 2	22	1.661

318	c	JVN061	Juvenile Arthritis	56	1.658

319		LYM133	Lymphoma, Hodgkin, Classic	74	1.600

320		SPN186	Spinal Cord Injury	61	1.600

321	c	SCN036	Secondary Progressive Multiple Sclerosis	55	1.600

322		INT323	Intraocular Pressure Quantitative Trait Locus	64	1.600

323		MYL069	Myeloma, Multiple	77	1.600

324	P	THY032	Thyroiditis	57	1.600

325	P	MTR014	Motor Neuron Disease	65	1.600

326	P	BNG032	Benign Mesothelioma	53	1.600

327		VSC002	Vascular Dementia	60	1.600

328		END072	Endotheliitis	36	1.590

329		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	1.590

330		NNL006	Non-Alcoholic Steatohepatitis	54	1.588

331		IMM167	Immune Deficiency Disease	78	1.588

332		CHC001	Chickenpox	57	1.588

333	c	VRL010	Viral Hepatitis	53	1.588

334		CRT015	Carotid Artery Occlusion	45	1.588

335	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	1.569

336		LYM017	Lyme Disease	62	1.569

337		STR067	Stroke, Ischemic	80	1.551

338		PRT036	Peritonitis	65	1.551

339		STT001	Status Epilepticus	59	1.551

340		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	1.536

341		ANR007	Anorexia Nervosa	60	1.536

342	P	MYC084	Mycobacterium Tuberculosis 1	68	1.536

343		PLY150	Polykaryocytosis Inducer	29	1.536

344		DSS032	Disease by Infectious Agent	55	1.536

345		LNG091	Lung Mucoepidermoid Carcinoma	32	1.536

346		OBS082	Obstructive Nephropathy	41	1.536

347		MCP006	Mucoepidermoid Carcinoma	48	1.536

348		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	1.536

349		CHG001	Chagas Disease	66	1.536

350	P	HYD006	Hydrocephalus	61	1.536

351		HML018	Homologous Wasting Disease	21	1.536

352	P	HNT016	Huntington Disease	73	1.505

353	P	HYP086	Hypothyroidism	69	1.505

354		GST033	Gestational Diabetes	61	1.505

355	c	PRM038	Primary Agammaglobulinemia	47	1.488

356	c	SPS158	Spastic Paraplegia 9a, Autosomal Dominant	44	1.485

357	P	BLD134	Bladder Cancer	79	1.467

358		SMT004	Smith-Lemli-Opitz Syndrome	70	1.467

359	c	ATR087	Atrial Standstill 1	74	1.467

360	c	CLC042	Celiac Disease 9	14	1.467

361	P	MPL001	Maple Syrup Urine Disease	70	1.467

362		PHN003	Phenylketonuria	76	1.467

363	P	BCL017	B-Cell Lymphoma	59	1.467

364	P	ACN011	Acne	57	1.467

365		TLN003	Telangiectasis	51	1.467

366		SYS003	Systolic Heart Failure	49	1.467

367	P	MYC033	Myoclonus	47	1.467

368		HMP009	Haemophilus Influenzae	41	1.467

369	c	MCR115	Microvascular Complications of Diabetes 5	65	1.457

370		AND005	Androgen Insensitivity Syndrome, Mild	21	1.433

371	P	DYS154	Dystonia	64	1.419

372	c	MTC200	Mitochondrial Dna Depletion Syndrome 17	20	1.413

373		CRB004	Cerebral Artery Occlusion	45	1.407

374		RFR013	Refractory Celiac Disease	33	1.393

375	P	HYP111	Hyperprolinemia	45	1.393

376		SXL003	Sexual Disorder	49	1.393

377		HLC007	Helicobacter Pylori Infection	67	1.393

378		LYM143	Lymphoma, Non-Hodgkin, Familial	75	1.393

379	P	ASP006	Aspergillosis	72	1.393

380		GYR004	Gyrate Atrophy of Choroid and Retina	58	1.393

381	c	FML116	Familial Cold Autoinflammatory Syndrome 1	55	1.393

382		GLC003	Glucose Intolerance	54	1.393

383		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	1.393

384	P	MYG005	Myoglobinuria	40	1.393

385	P	TRT010	Teratoma	51	1.393

386		MRP001	Morphine Dependence	42	1.393

387		CRY004	Cryoglobulinemia	48	1.393

388		GST023	Gastric Ulcer	52	1.393

389		TLR001	Tularemia	56	1.393

390		RHM014	Rheumatoid Vasculitis	37	1.393

391	P	CLS010	Cluster Headache	42	1.393

392	c	MYT029	Myotonia Congenita, Autosomal Recessive	40	1.391

393		END021	Endomyocardial Fibrosis	56	1.391

394	c	BDY021	Body Mass Index Quantitative Trait Locus 20	49	1.376

395	P	SZR006	Seizure Disorder	70	1.356

396		INS024	Insulin-Like Growth Factor I	78	1.356

397		CYS001	Cystic Fibrosis	78	1.356

398		ART016	Aortic Aneurysm	68	1.356

399		PMP006	Pemphigus Vulgaris, Familial	58	1.319

400	P	PMP001	Pemphigus	55	1.319

401	P	RBL001	Rubella	58	1.319

402	P	EYD002	Eye Disease	57	1.319

403		GST009	Gastroschisis	53	1.313

404		SMT017	Somatomammotropinoma	17	1.313

405		PTT048	Pituitary Adenoma, Prolactin-Secreting	64	1.313

406	P	LKM071	Leukemia, Chronic Lymphocytic	75	1.313

407	P	PRK057	Parkinson Disease, Late-Onset	80	1.313

408		HYP780	Hypoadrenocorticism, Familial	61	1.313

409		PLG003	Polg-Related Disorders	20	1.313

410		DST006	Diastolic Heart Failure	45	1.313

411	P	ENC004	Encephalitis	61	1.313

412		ABD010	Abdominal Wall Defect	39	1.313

413		BNS003	Binswanger's Disease	41	1.313

414		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	1.303

415	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	1.303

416	P	HYP750	Hypertriglyceridemia, Familial	62	1.303

417		CHR100	Chronic Ulcer of Skin	57	1.248

418		HYP056	Hypoglycemia	65	1.248

419		NTR005	Nutritional Deficiency Disease	61	1.235

420		INT276	Interatrial Communication	51	1.227

421		TRG019	Trigonocephaly with Short Stature and Developmental Delay	38	1.227

422	P	ATR010	Atrial Heart Septal Defect	58	1.227

423		KPS004	Kaposi Sarcoma	77	1.224

424		ARG004	Argyria	26	1.224

425	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	1.224

426		XLN228	X-Linked Recessive Disease	24	1.224

427	P	CHL066	Cholangitis	52	1.224

428	c	HMG001	Hemoglobin C Disease	41	1.224

429		UND007	Undifferentiated Connective Tissue Disease	28	1.224

430	P	CHR345	Chronic Pain	50	1.224

431		RMT001	Remitting Seronegative Symmetrical Synovitis with Pitting Edema	17	1.224

432		MTC112	Mitochondrial Dna-Associated Leigh Syndrome	32	1.205

433		SPS057	Spasticity	42	1.190

434		HMC014	Homocysteinemia	52	1.190

435	P	END033	Endocarditis	58	1.190

436		PLM033	Pulmonary Embolism	58	1.190

437	P	DRM053	Dermatitis, Atopic	65	1.128

438	P	MJR001	Major Depressive Disorder	68	1.128

439		CHL067	Cholecystitis	60	1.128

440		MNT002	Mental Depression	57	1.128

441		ILS001	Ileus	50	1.128

442		DYS064	Dystonia 3, Torsion, X-Linked	45	1.123

443	c	MST023	Mesothelioma, Malignant	56	1.123

444	c	SYS045	Systemic Lupus Erythematosus 14	13	1.123

445		KRT019	Keratitis, Hereditary	66	1.123

446	c	CTS029	Cutis Laxa, Autosomal Recessive, Type Iiia	53	1.123

447		MLT157	Multiple System Atrophy 1	69	1.123

448	P	CRY007	Cryoglobulinemia, Familial Mixed	49	1.123

449	P	PRK039	Parkinsonism	55	1.123

450		SCN068	Secondary Interstitial Lung Disease in Childhood and Adulthood Associated with a Connective Tissue Disease	19	1.123

451	P	HYP098	Hypereosinophilic Syndrome	66	1.123

452	P	CYS018	Cystitis	59	1.123

453	P	RTN016	Retinal Degeneration	52	1.123

454		BRN012	Bronchiolitis Obliterans	56	1.123

455		HYP068	Hyperostosis	47	1.123

456		MNN009	Meningoencephalitis	48	1.123

457		SPT004	Septic Arthritis	58	1.123

458		MLT016	Multicentric Reticulohistiocytosis	39	1.123

459	c	SVR005	Severe Pre-Eclampsia	50	1.123

460		HRP004	Herpes Zoster	61	1.123

461		KDN013	Kidney Hypertrophy	34	1.123

462	P	OVR042	Ovarian Cancer	88	1.064

463	P	BRS047	Breast Cancer	98	1.064

464	P	ANP001	Anaplastic Large Cell Lymphoma	61	1.064

465	P	URN019	Urinary Tract Infection	49	1.064

466	P	LKM062	Leukemia, Acute Lymphoblastic	69	1.064

467		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	1.064

468	c	ATS307	Autosomal Recessive Cerebellar Ataxia	39	1.064

469	P	AMY004	Amyloidosis	70	1.064

470		LRN003	Learning Disability	49	1.064

471		RHM036	Rheumatoid Arthritis Interstitial Lung Disease	31	1.064

472	P	PLM006	Pulmonary Alveolar Proteinosis	53	1.064

473		BLR001	Biliary Atresia	55	1.064

474		PST106	Post-Cardiac Arrest Syndrome	31	1.064

475	P	KDN017	Kidney Cancer	61	1.064

476		SBC016	Subacute Delirium	43	1.064

477	c	SCN046	Secondary Short Bowel Syndrome	14	1.036

478		PHS029	Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic	26	1.036

479		GST050	Gastrointestinal System Disease	55	1.028

480		DSR072	Disorder of Energy Metabolism	10	1.013

481	P	PRC031	Preeclampsia/eclampsia 1	43	1.013

482	c	HYP724	Hyperlipoproteinemia, Type Iii	67	1.013

483		AGG012	Aggressive Nk-Cell Leukemia	46	1.013

484		PST020	Postpoliomyelitis Syndrome	43	1.013

485		HRT015	Heritable Pulmonary Arterial Hypertension	46	1.013

486	P	MYS003	Myasthenia Gravis	68	1.004

487		OTT002	Otitis Media	71	1.004

488		CHR005	Chorioamnionitis	50	1.004

489	P	FML011	Familial Adenomatous Polyposis	71	1.004

490		CHK001	Chikungunya	60	1.004

491		PMP004	Pemphigus Foliaceus	43	1.004

492		TQP001	Taqi Polymorphism	29	1.004

493		CVT001	Cavitary Optic Disc Anomalies	37	1.004

494		HYD003	Hydrarthrosis	30	1.004

495	P	RHB003	Rhabdomyosarcoma	66	1.004

496		INT182	Intermittent Hydrarthrosis	17	1.004

497		IGG001	Iga Glomerulonephritis	50	1.004

498		BRD005	Borderline Leprosy	28	1.004

499		RFL002	Reflex Epilepsy	41	1.004

500		SPP004	Suppurative Cholangitis	23	1.004

501		IDP011	Idiopathic Interstitial Pneumonia	59	1.004

502		LPR001	Lepromatous Leprosy	49	1.004

503		TBR006	Tuberculoid Leprosy	43	1.004

504	P	OBS001	Obstructive Jaundice	48	1.004

505	P	SCL015	Scleritis	48	1.004

506		PST046	Post-Transplant Lymphoproliferative Disease	53	1.004

507	P	PHC003	Pheochromocytoma	69	0.995

508		ADR040	Adrenal Gland Pheochromocytoma	46	0.995

509		GLB002	Glioblastoma	67	0.995

510		PRP016	Paraplegia	52	0.995

511	P	LKM002	Leukemia	67	0.995

512	c	ACT068	Acute Cystitis	61	0.995

513	P	MCR010	Microcephaly	60	0.995

514	P	CTS001	Cutis Laxa	65	0.995

515	P	ACT105	Acute Mountain Sickness	52	0.995

516	P	OVR082	Overgrowth Syndrome	49	0.921

517		INF034	Infective Endocarditis	54	0.921

518		MLD018	Mild Cognitive Impairment	48	0.921

519		VRC005	Varicose Veins	60	0.921

520	P	NRB001	Neuroblastoma	66	0.921

521	P	HRP006	Herpes Simplex	65	0.921

522	P	HML002	Hemolytic Anemia	62	0.921

523	P	ALP008	Alopecia	54	0.921

524	P	THR014	Thrombocytopenia	66	0.921

525		BLR008	Bilirubin Metabolic Disorder	57	0.921

526		CHL014	Cholera	62	0.921

527		ESP002	Esophageal Varix	51	0.921

528		DSS009	Disseminated Intravascular Coagulation	57	0.921

529	c	FML021	Familial Hypercholesterolemia	72	0.921

530	P	PLY019	Polyneuropathy	52	0.921

531		ADL030	Adult-Onset Still's Disease	59	0.921

532		IRN002	Iron Metabolism Disease	57	0.921

533		CRB037	Cerebral Palsy	67	0.921

534		AMN006	Aminoaciduria	37	0.921

535	c	HMC039	Hemochromatosis, Type 1	73	0.848

536		RST023	Resting Heart Rate, Variation in	40	0.848

537		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.848

538	c	RTN047	Retinitis Pigmentosa 18	46	0.848

539		DFF005	Diffuse Large B-Cell Lymphoma	54	0.848

540		CRS005	Crest Syndrome	36	0.848

541	c	SPN226	Spondyloarthropathy 2	15	0.848

542	c	SYS046	Systemic Lupus Erythematosus 3	18	0.848

543		ALV005	Alveolar Soft Part Sarcoma	61	0.848

544	c	PSR033	Psoriasis 12	26	0.848

545		ORB013	Orbital Disease	42	0.848

546	P	BCL004	B-Cell Non-Hodgkin Lymphoma	42	0.848

547	P	EPL164	Epilepsy	68	0.848

548		MNC006	Monoclonal Gammopathy of Uncertain Significance	47	0.848

549		EXT034	Extrinsic Allergic Alveolitis	57	0.848

550	c	ACT004	Acute Diarrhea	40	0.848

551		CRY001	Cryptogenic Organizing Pneumonia	54	0.848

552		FRZ001	Frozen Shoulder	55	0.848

553		EXS001	Exostosis	49	0.848

554		BRS064	Bursitis	51	0.848

555		SCL011	Sclerosing Keratitis	24	0.848

556		CLC006	Calcinosis	47	0.848

557	P	MRC003	Mercury Poisoning	49	0.848

558		RTB001	Rat Bite Fever	26	0.848

559		CHR178	Chromosomal Triplication	34	0.848

560	P	RTN008	Retinitis Pigmentosa	80	0.841

561		NRP045	Neuropathy, Ataxia, and Retinitis Pigmentosa	47	0.841

562		RTN017	Retinal Detachment	60	0.841

563		MRF001	Marfan Syndrome	76	0.841

564	P	MCR129	Microvascular Complications of Diabetes 1	68	0.841

565	P	GST053	Gastric Cancer	83	0.841

566	P	GLC113	Galactosemia I	66	0.841

567	P	GLM040	Glioma Susceptibility 1	71	0.841

568		HRW001	Hair Whorl	35	0.841

569		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	60	0.841

570		ORG002	Organic Acidemia	44	0.841

571		NRR001	Neuroretinitis	42	0.841

572	c	ACT075	Acute Myocardial Infarction	56	0.841

573		RTN023	Retinitis	46	0.841

574	P	HMC002	Homocystinuria	53	0.841

575	P	MYL006	Myeloid Leukemia	61	0.841

576	P	MTH008	Methylmalonic Acidemia	52	0.841

577	P	BRS044	Breast Adenocarcinoma	58	0.841

578		APP008	Appendicitis	62	0.841

579		MLG079	Malignant Pleural Mesothelioma	42	0.841

580	c	MCR112	Microvascular Complications of Diabetes 2	42	0.841

581	P	HMP002	Hemophagocytic Lymphohistiocytosis	61	0.841

582	P	GRV001	Graves' Disease	55	0.841

583		DNT012	Dental Caries	53	0.841

584		PYL006	Pyloric Stenosis	48	0.841

585		MLG169	Malignant Astrocytoma	57	0.841

586		HNC001	Henoch-Schoenlein Purpura	54	0.841

587	P	RHN004	Rhinitis	57	0.841

588		THY030	Thyroid Gland Disease	50	0.841

589	P	INF032	Infertility	57	0.841

590	P	HYP076	Hyperthyroidism	53	0.841

591	P	ART021	Arteriosclerosis	54	0.841

592		PLG002	Plague	58	0.841

593		PLM010	Pulmonary Edema	55	0.841

594		KRT001	Keratoconjunctivitis Sicca	50	0.841

595	c	MTC014	Mitochondrial Dna Deletion Syndromes	16	0.841

596		THR123	Thrombotic Microangiopathy	40	0.752

597	c	SPR086	Spermatogenic Failure 3	46	0.752

598		HYP003	Hypermethioninemia	51	0.752

599		MSC007	Muscle Hypertrophy	64	0.752

600		CHL152	Childhood Acute Lymphocytic Leukemia	50	0.752

601	P	CRP001	Carpal Tunnel Syndrome	66	0.752

602	c	CTR129	Cataract 31, Multiple Types	36	0.752

603	c	SPS159	Spastic Paraplegia 9b, Autosomal Recessive	40	0.752

604	P	TYR004	Tyrosinemia	50	0.752

605		PRP007	Priapism	47	0.752

606		PRC013	Pericarditis	53	0.752

607	P	GST044	Gastritis	55	0.752

608		ACT049	Acute Disseminated Encephalomyelitis	48	0.752

609		PRP009	Peripartum Cardiomyopathy	55	0.752

610		CRN017	Coronary Thrombosis	46	0.752

611		ASP003	Aseptic Meningitis	50	0.752

612		DYS015	Dysentery	50	0.752

613		PNC001	Pancytopenia	53	0.752

614		ALC006	Alcoholic Hepatitis	61	0.752

615		CNS004	Constipation	56	0.752

616	P	HMN010	Hemangioma	62	0.752

617	P	NPH012	Nephrotic Syndrome	60	0.752

618	c	HRD010	Hereditary Spastic Paraplegia	66	0.752

619		CLN015	Colon Adenocarcinoma	65	0.752

620		HMP001	Hemopericardium	47	0.752

621		CRD001	Cardiac Tamponade	43	0.752

622	P	PRC012	Pericardial Effusion	50	0.752

623		ALC005	Alcoholic Pancreatitis	38	0.752

624		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.752

625		SFT003	Soft Tissue Sarcoma	57	0.752

626		BCK006	Back Pain	47	0.752

627		ANR040	Aneurysm	61	0.752

628	c	DVL105	Developmental and Epileptic Encephalopathy 82	23	0.733

629	c	BLD140	Blood Group, I System	46	0.702

630		CHY002	Chylomicron Retention Disease	64	0.702

631	c	INF071	Inflammatory Bowel Disease 1	65	0.702

632	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	63	0.702

633	P	ATS364	Autism	69	0.652

634		DFF031	Diffuse Alveolar Hemorrhage	31	0.652

635	c	SPS042	Spastic Paraplegia 9	21	0.652

636		STN013	Stenotrophomonas Maltophilia Infection	26	0.652

637		SQM013	Squamous Cell Carcinoma, Head and Neck	73	0.652

638		PRS127	Pearson Marrow-Pancreas Syndrome	52	0.652

639	P	SCH015	Schizophrenia	74	0.652

640	c	EXD008	Exudative Vitreoretinopathy 1	71	0.652

641		ALC007	Alcohol Dependence	66	0.652

642		3HY001	3-Hydroxyisobutyric Aciduria	26	0.652

643	P	HYP769	Hyperlysinemia, Type I	42	0.652

644		HMN044	Human Immunodeficiency Virus Type 1	78	0.652

645		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	57	0.652

646		ANG054	Angina Pectoris	66	0.652

647	P	ADL017	Adult T-Cell Leukemia	56	0.652

648		WST001	West Syndrome	59	0.652

649	c	CHR711	Chronic Asthma	41	0.652

650	P	FTL001	Fetal Alcohol Syndrome	55	0.652

651		KRN002	Kearns-Sayre Syndrome	63	0.652

652	c	BRN108	Branchiootic Syndrome 1	62	0.652

653	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.652

654	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	63	0.652

655	c	CTS041	Cutis Laxa, Autosomal Dominant 3	45	0.652

656		PRT082	Preterm Premature Rupture of the Membranes	57	0.652

657		THY029	Thyroid Carcinoma	51	0.652

658		CWP001	Cowpox	45	0.652

659		CMP010	Complex Regional Pain Syndrome	60	0.652

660	P	PLY017	Polyarteritis Nodosa	60	0.652

661	P	RNV001	Renovascular Hypertension	49	0.652

662	P	CHR012	Chronic Granulomatous Disease	69	0.652

663		VCC001	Vaccinia	47	0.652

664	P	CND004	Candidiasis	58	0.652

665	P	AGN002	Agnosia	54	0.652

666		PPT005	Peptic Ulcer Disease	58	0.652

667		LYM027	Lymphopenia	56	0.652

668		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.652

669		XRP001	Xerophthalmia	41	0.652

670		PLR008	Pleurisy	50	0.652

671		HMS001	Hemosiderosis	48	0.652

672	P	MLN007	Male Infertility	56	0.652

673		ACR007	Acromegaly	70	0.652

674		RTN020	Retinal Vascular Disease	46	0.652

675		NNT012	Neonatal Jaundice	53	0.652

676		URT001	Urethritis	53	0.652

677		IRN001	Iron Deficiency Anemia	58	0.652

678		MST005	Mastitis	53	0.652

679	P	FNC004	Fanconi Syndrome	60	0.652

680		BRN024	Bronchitis	67	0.652

681		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	46	0.652

682	P	CRV039	Cervicitis	52	0.652

683		PLS007	Plasmodium Falciparum Malaria	52	0.652

684		PNN001	Panniculitis	52	0.652

685	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	60	0.652

686	P	HYP009	Hypertrophic Pyloric Stenosis	41	0.652

687		HDR002	Hidradenitis Suppurativa	54	0.652

688		HDR003	Hidradenitis	50	0.652

689		SQM006	Squamous Cell Carcinoma	60	0.652

690		ISL099	Isolated Methylmalonic Acidemia	36	0.652

691		NRF007	Neurofibroma	64	0.652

692		IRR002	Irritable Bowel Syndrome	65	0.652

693	c	LKM005	Leukemia, T-Cell, Chronic	34	0.652

694	P	FML187	Familial Hypertension	34	0.652

695		SNG003	Single Ventricular Heart	30	0.532

696		GRW007	Growth Hormone Deficiency	46	0.532

697		ADR022	Adrenomyeloneuropathy	39	0.532

698	P	AVS003	Avascular Necrosis	41	0.532

699		SPS019	Spastic Paraparesis	38	0.532

700		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	45	0.532

701		FRN006	Frontotemporal Dementia	68	0.532

702		ADR007	Adrenoleukodystrophy	73	0.532

703	c	THY107	Thymoma, Familial	42	0.532

704		CRD132	Cardiac Conduction Defect	60	0.532

705		ACR056	Acrodermatitis Enteropathica, Zinc-Deficiency Type	56	0.532

706		ALL003	Allergic Rhinitis	67	0.532

707		MTC029	Mitochondrial Complex V Deficiency, Nuclear Type 1	40	0.532

708	c	PSR029	Psoriasis 9	24	0.532

709		ANX010	Anxiety	70	0.532

710	c	PNC108	Pancreatitis, Hereditary	69	0.532

711		BRK010	Burkitt Lymphoma	66	0.532

712	P	ATX030	Ataxia-Telangiectasia	80	0.532

713		NRD100	Neurodevelopmental, Jaw, Eye, and Digital Syndrome	49	0.532

714		FDB001	Foodborne Botulism	55	0.532

715	P	MLT008	Multinodular Goiter	42	0.532

716		ALC001	Alcohol-Related Birth Defect	36	0.532

717	c	MJR022	Major Affective Disorder 8	38	0.532

718		PYR012	Pyruvate Dehydrogenase E1-Beta Deficiency	41	0.532

719		LMB062	Limb Ischemia	55	0.532

720		TND005	Tendinitis	54	0.532

721		PYR010	Peyronie's Disease	50	0.532

722	P	ERY036	Erythema Nodosum	49	0.532

723	c	ATS007	Autism Spectrum Disorder	72	0.532

724	P	PLY014	Polycystic Kidney Disease	69	0.532

725	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	0.532

726		APH002	Aphasia	56	0.532

727		ILT001	Ileitis	48	0.532

728		HPT046	Hepatic Veno-Occlusive Disease	62	0.532

729	c	ATM022	Autoimmune Myocarditis	36	0.532

730	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	0.532

731		NRL016	Neural Tube Defects	81	0.532

732	c	DPH024	Diaphragmatic Hernia, Congenital	64	0.532

733		PRP001	Propionic Acidemia	65	0.532

734		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.532

735	c	MJR024	Major Affective Disorder 9	41	0.532

736	c	CHL119	Cholangitis, Primary Sclerosing	58	0.532

737		PRL045	Proline-Negative Auxotroph of Hamster, Complementation of	16	0.532

738	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	0.532

739	P	SPP010	Suppressor of Tumorigenicity 3	51	0.532

740	c	PYL018	Pyloric Stenosis, Infantile Hypertrophic, 1	35	0.532

741	P	STR020	Strabismus	56	0.532

742	P	UNC017	Uncombable Hair Syndrome 1	32	0.532

743	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	0.532

744	P	CRC039	Coarctation of Aorta	46	0.532

745		DNB001	Danubian Endemic Familial Nephropathy	41	0.532

746		MYL057	Myelopathy, Htlv-1-Associated	38	0.532

747		HND015	Hand Skill, Relative	30	0.532

748	P	HRS035	Hirschsprung Disease 1	66	0.532

749		AMY087	Amyloidosis, Hereditary, Transthyretin-Related	65	0.532

750		PLM124	Pulmonary Hypertension, Neonatal	20	0.532

751		OST017	Osteomyelitis	63	0.532

752	P	PLY188	Polyendocrinopathy	31	0.532

753		PMP014	Pemphigoid	51	0.532

754	P	MYP006	Myopia	56	0.532

755	P	LCH002	Lichen Planus	54	0.532

756		INT075	Intracranial Hypertension	53	0.532

757		ACH005	Achalasia	55	0.532

758		MCH006	Mechanical Strabismus	40	0.532

759		KRT006	Keratoconjunctivitis	53	0.532

760	P	MTC133	Mitochondrial Myopathy	50	0.532

761		DBT010	Diabetic Neuropathy	54	0.532

762	P	RRH023	Rare Hereditary Hemochromatosis	54	0.532

763	P	ALC033	Alcohol Use Disorder	61	0.532

764	P	PTT006	Pituitary Adenoma	55	0.532

765	P	BPL003	Bipolar Disorder	56	0.532

766	P	FBR017	Fibrosarcoma	56	0.532

767	P	MST009	Mastocytosis	64	0.532

768		PNM008	Pneumothorax	54	0.532

769		CRV038	Cervical Squamous Cell Carcinoma	58	0.532

770	P	SYP003	Syphilis	59	0.532

771		HRT012	Heart Valve Disease	53	0.532

772	P	NLD001	Nail Disease	51	0.532

773	c	VRL007	Viral Encephalitis	50	0.532

774	P	INF038	Influenza	68	0.532

775		BLL006	Bullous Pemphigoid	61	0.532

776	P	MMB011	Membranous Nephropathy	50	0.532

777	P	CRN024	Corneal Disease	44	0.532

778		NSP002	Nasopharyngitis	45	0.532

779	c	ATM104	Autoimmune Vasculitis	37	0.532

780		INT060	Intestinal Atresia	41	0.532

781	P	HYP061	Hypertrophic Cardiomyopathy	69	0.532

782		GTR002	Goiter	53	0.532

783		TRN015	Transient Cerebral Ischemia	63	0.532

784	P	PST095	Post-Thrombotic Syndrome	51	0.532

785		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.532

786	P	SCL009	Sclerosing Cholangitis	48	0.532

787		NRT004	Neuritis	53	0.532

788		HYP072	Hypersensitivity Reaction Type Iii Disease	39	0.532

789		KRT009	Keratosis	53	0.532

790		GLS001	Gliosarcoma	64	0.532

791		PPL018	Papillary Adenocarcinoma	44	0.532

792	P	INT143	Interstitial Cystitis	60	0.532

793		PRS036	Parasitic Protozoa Infectious Disease	44	0.532

794		HPT014	Hepatorenal Syndrome	49	0.532

795	P	THR005	Thrombotic Thrombocytopenic Purpura	64	0.532

796	P	BND020	Bone Disease	59	0.532

797		PLP001	Pulpitis	48	0.532

798		CHL123	Chlamydia	58	0.532

799	P	CHN059	Chondrocalcinosis	52	0.532

800	c	VRL005	Viral Pneumonia	53	0.532

801		HMN014	Human Immunodeficiency Virus Infectious Disease	54	0.532

802		OST016	Osteochondrosis	52	0.532

803		BRS099	Breast Ductal Carcinoma	61	0.532

804		CYS009	Cystadenoma	43	0.532

805		ACR005	Acrodermatitis	38	0.532

806	P	THY023	Thymoma	64	0.532

807	c	CNT035	Central Nervous System Disease	54	0.532

808		MDD011	Mood Disorder	62	0.532

809		DRM006	Dermatitis	62	0.532

810		TRP002	Tropical Spastic Paraparesis	49	0.532

811		TYP007	Typhoid Fever	64	0.532

812	P	GND004	Gonadal Dysgenesis	47	0.532

813		EXC002	Exocrine Pancreatic Insufficiency	42	0.532

814		FML035	Familial Hyperlipidemia	55	0.532

815		MGC001	Megacolon	48	0.532

816		AMN003	Amnestic Disorder	54	0.532

817		QDR001	Quadriplegia	50	0.532

818		HYP014	Hyperuricemia	51	0.532

819		HYP080	Hypogonadism	50	0.532

820		HST011	Histoplasmosis	55	0.532

821		PST028	Post-Traumatic Stress Disorder	59	0.532

822		NCR007	Necrotizing Fasciitis	49	0.532

823		HYP141	Hyperphenylalaninemia	42	0.532

824	P	INS002	in Situ Carcinoma	53	0.532

825		FSC004	Fasciitis	49	0.532

826	P	TXP001	Toxoplasmosis	60	0.532

827		STM007	Stomatitis	54	0.532

828		HTL001	Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis	38	0.532

829		MST020	Mast Cell Activation Syndrome	28	0.532

830		TRC096	Trichothiodystrophy	55	0.532

831		HDN002	Head Injury	44	0.532

832		MCR225	Macrophage Activation Syndrome	45	0.532

833	c	ATM075	Autoimmune Encephalitis	40	0.532

834		ENT007	Enteropathica	25	0.532

835	P	NRV007	Nervous System Disease	67	0.532

836	c	HMN021	Human T-Cell Leukemia Virus Type 1	47	0.532

837		MTT004	Metatarsus Adductus	17	0.532

838		ATN011	Autoinflammation with Infantile Enterocolitis	45	0.496

839		RSP019	Respiratory Distress Syndrome in Premature Infants	52	0.496

840	P	ANR048	Aniridia 1	64	0.496

841		CHR661	Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction	49	0.496

842	c	DRR009	Diarrhea 6	45	0.496

843		TRP004	Tropical Sprue	39	0.496

844		ENT001	Enterocele	42	0.496

845	P	CMP008	Compartment Syndrome	50	0.496

846	P	CLL015	Collagen Disease	48	0.496

847		RSP007	Respiratory Distress Syndrome, Infant	40	0.496

848		DDN006	Duodenitis	50	0.496

849	c	ATS392	Autosomal Recessive Cutis Laxa Type Iii	48	0.472

850		GRN020	Granulomatous Hypophysitis	14	0.472

851		DMN042	Diaminopentanuria	14	0.376

852		RNL024	Renal Glucosuria	60	0.376

853		CLF004	Cleft Lip/palate	57	0.376

854		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	42	0.376

855		PCH007	Pouchitis	42	0.376

856	P	NNT042	Neonatal Lupus Erythematosus	37	0.376

857		ERY014	Erythrokeratoderma	26	0.376

858		MTR087	Maternal Uniparental Disomy	28	0.376

859	P	HRD217	Hereditary Optic Neuropathy	36	0.376

860		GRN033	Granulomatous Mastitis	32	0.376

861	c	INH030	Inherited Retinal Disorder	28	0.376

862		SMT007	Smith-Fineman-Myers Syndrome	32	0.376

863		THP001	Thiopurine S Methyltranferase Deficiency	20	0.376

864	P	THL005	Thalassemia	56	0.376

865		SDD008	Sudden Sensorineural Hearing Loss	41	0.376

866		CNG491	Congenital Portosystemic Shunt	17	0.376

867		PFF001	Pfeiffer Syndrome	77	0.376

868	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.376

869	P	NSP012	Nasopharyngeal Carcinoma	61	0.376

870	c	CRD186	Ceroid Lipofuscinosis, Neuronal, 3	63	0.376

871		FMR004	Fumarase Deficiency	50	0.376

872	c	DRM040	Dermatitis Herpetiformis, Familial	35	0.376

873		BRT054	Brittle Bone Disorder	74	0.376

874		LPM012	Lipomatosis, Multiple	60	0.376

875	P	MCR364	Macrodactyly	40	0.376

876		PRL019	Prolidase Deficiency	50	0.376

877		CRD002	Cri-Du-Chat Syndrome	49	0.376

878		EPD002	Epidermolytic Hyperkeratosis	56	0.376

879		GST092	Gastroesophageal Reflux	61	0.376

880		VLV047	Volvulus of Midgut	52	0.376

881	P	PTY003	Pityriasis Rubra Pilaris	57	0.376

882		PRG071	Progressive Pseudorheumatoid Dysplasia	45	0.376

883	c	FNC027	Fanconi Anemia, Complementation Group a	81	0.376

884		ISV001	Isovaleric Acidemia	54	0.376

885		HYP001	Hypochromic Microcytic Anemia	37	0.376

886		FTL006	Fetal Alcohol Spectrum Disorder	43	0.376

887		MNT001	Mantle Cell Lymphoma	67	0.376

888		MYL009	Myelodysplastic Syndrome	67	0.376

889		BTN004	Biotin Deficiency	45	0.376

890		HYP346	Hypotrichosis and Recurrent Skin Vesicles	29	0.376

891		NRN005	Neuronal Ceroid-Lipofuscinoses	61	0.376

892		KSH004	Kashin-Beck Disease	38	0.376

893		IGG007	Igg4-Related Disease	48	0.376

894		ART074	Aortic Dissection	53	0.376

895		C1N001	C1 Inhibitor Deficiency	43	0.376

896		APR001	Apraxia	52	0.376

897	P	ATR011	Atrial Fibrillation	66	0.376

898		RSP021	Respiratory Allergy	41	0.376

899	P	LYM033	Lymphoproliferative Syndrome	59	0.376

900		INT072	Intestinal Pseudo-Obstruction	62	0.376

901		HYP025	Hyperphosphatemia	48	0.376

902	P	BRC006	Brachydactyly	51	0.376

903		LMB024	Limbic Encephalitis	43	0.376

904	c	RTN041	Retinitis Pigmentosa 11	42	0.376

905	P	FNC044	Fanconi Anemia, Complementation Group C	56	0.376

906	c	FNC042	Fanconi Anemia, Complementation Group D2	54	0.376

907		GLT014	Glutathionuria	37	0.376

908		GDP001	Goodpasture Syndrome	55	0.376

909		TRD006	Tardive Dyskinesia	53	0.376

910	c	GRV008	Graves Disease 1	54	0.376

911		CHR288	Chronic Recurrent Multifocal Osteomyelitis	60	0.376

912	c	CHR627	Charcot-Marie-Tooth Disease, Demyelinating, Type 1a	56	0.376

913	c	CHR320	Chiari Malformation Type I	46	0.376

914		ICH001	Ichthyosis Vulgaris	53	0.376

915		SPN019	Spondylolisthesis	52	0.376

916	P	PRD006	Prader-Willi Syndrome	61	0.376

917	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.376

918		LGH019	Light Fixation Seizure Syndrome	27	0.376

919		LNG108	Langerhans Cell Histiocytosis	58	0.376

920		BLD063	Bile Duct Cysts	42	0.376

921		CNG510	Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi	63	0.376

922		AKL001	Au-Kline Syndrome	39	0.376

923		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	44	0.376

924		EWN003	Ewing Sarcoma	70	0.376

925		TMP012	Temple Syndrome	38	0.376

926		ACT119	Acute Promyelocytic Leukemia	62	0.376

927		MTC068	Mitochondrial Complex V Deficiency, Nuclear Type 2	31	0.376

928	c	SYS040	Systemic Lupus Erythematosus 10	22	0.376

929		SCC002	Saccharopinuria	26	0.376

930	c	ANM035	Anemia, Hypochromic Microcytic, with Iron Overload 1	36	0.376

931		LBR038	Leber Hereditary Optic Neuropathy, Modifier of	62	0.376

932	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	0.376

933	P	HRT035	Heart Block, Congenital	43	0.376

934	c	PLM167	Pulmonary Venoocclusive Disease 2, Autosomal Recessive	38	0.376

935	P	HYP058	Hypervitaminosis a	47	0.376

936		INT303	Intracranial Hypertension, Idiopathic	56	0.376

937		LRN002	Laron Syndrome	63	0.376

938		THR100	Thrombocytopenic Purpura, Autoimmune	61	0.376

939	P	PLM085	Pulmonary Hemosiderosis	44	0.376

940	P	MJR007	Major Affective Disorder 1	42	0.376

941		INC002	Inclusion Body Myositis	57	0.376

942		CMP040	Complement Component 4, Partial Deficiency of	34	0.376

943		OPT066	Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy	55	0.376

944		DMN031	Dementia, Lewy Body	65	0.376

945		DYS053	Dystelephalangy	14	0.376

946	P	PYR039	Peyronie Disease	39	0.376

947	P	MYP105	Myopathy, Myosin Storage, Autosomal Dominant	40	0.376

948	c	SYS069	Systemic Lupus Erythematosus 6	21	0.376

949