Search results for Carbon dioxide

1160 hits were found for Carbon dioxide

#	Family	MCID	Name	MIFTS	Score
1		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.319

2	P	RSP003	Respiratory Failure	74	0.316

3		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.315

4	P	CRD119	Cardiac Arrest	67	0.301

5		HYP266	Hypoxia	57	0.257

6		LNG099	Lung Disease	60	0.240

7		MTB004	Metabolic Acidosis	50	0.231

8	P	PNC025	Panic Disorder	53	0.229

9		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.220

10	P	KDN018	Kidney Disease	72	0.213

11		HRW001	Hair Whorl	36	0.209

12	c	NRF023	Neurofibromatosis, Type Ii	80	0.203

13		MTH071	Methane Production	26	0.198

14		OCL069	Ocular Motor Apraxia	51	0.198

15	c	DWL002	Dowling-Degos Disease 1	58	0.197

16		LVR012	Liver Cirrhosis	62	0.193

17	P	ENC018	Encephalopathy	61	0.181

18	c	CHR684	Chronic Kidney Disease	70	0.180

19		TXC005	Toxic Shock Syndrome	62	0.179

20		ANX004	Anoxia	40	0.174

21	P	LVR013	Liver Disease	68	0.163

22		ISC004	Ischemia	58	0.162

23	P	SLP006	Sleep Apnea	69	0.160

24	P	PLM037	Pulmonary Hypertension	67	0.157

25		ANX010	Anxiety	73	0.156

26		48X005	48,xyyy	39	0.156

27		ALL026	Allergic Hypersensitivity Disease	62	0.152

28		BRN024	Bronchitis	68	0.151

29	P	RHN004	Rhinitis	57	0.150

30	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.149

31		PLM010	Pulmonary Edema	54	0.146

32	P	VSC007	Vascular Disease	63	0.145

33		47X002	47,xyy	49	0.144

34		CNG034	Congestive Heart Failure	69	0.142

35	P	CLR023	Colorectal Cancer	99	0.142

36	P	PLM036	Pulmonary Fibrosis	65	0.141

37		PPL052	Papillomatosis, Confluent and Reticulated	33	0.140

38		ADN018	Adenoma	59	0.139

39		PNM008	Pneumothorax	56	0.138

40		CRB039	Cerebrovascular Disease	67	0.137

41		ALL003	Allergic Rhinitis	67	0.137

42		BNR002	Bone Resorption Disease	48	0.137

43		HLX001	Helix Syndrome	47	0.135

44	P	HPT023	Hepatocellular Carcinoma	100	0.134

45	c	CRV002	Cervix Uteri Carcinoma in Situ	46	0.132

46		CRV045	Cervical Intraepithelial Neoplasia	39	0.132

47	P	HDC001	Headache	57	0.129

48		PLM033	Pulmonary Embolism	59	0.129

49	P	HMN010	Hemangioma	61	0.124

50	P	LNG032	Lung Cancer	98	0.124

51	P	RNL007	Renal Tubular Acidosis	51	0.123

52	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.121

53	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.121

54	P	ADL010	Adult Respiratory Distress Syndrome	65	0.121

55		PRT036	Peritonitis	64	0.121

56		INT075	Intracranial Hypertension	53	0.119

57	P	PNC035	Pancreatic Cancer	84	0.118

58		PPL022	Papilloma	54	0.118

59	P	ADN016	Adenocarcinoma	64	0.118

60	P	SZR006	Seizure Disorder	56	0.118

61		SQM006	Squamous Cell Carcinoma	60	0.117

62		BRN071	Brain Injury	49	0.117

63		FTT001	Fatty Liver Disease	61	0.116

64		END086	End Stage Renal Disease	51	0.116

65		VSL002	Visual Epilepsy	59	0.115

66		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.115

67		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.114

68	P	PLM034	Pulmonary Emphysema	55	0.114

69		CYT002	Cytokine Deficiency	42	0.113

70		ART016	Aortic Aneurysm	69	0.113

71	P	NRB001	Neuroblastoma	72	0.112

72	P	END044	Endometriosis	63	0.111

73		LMB062	Limb Ischemia	55	0.111

74		PNG002	Pain Agnosia	51	0.111

75		AST005	Asthma	76	0.110

76		HYP457	Hypertrophic Scars	42	0.110

77	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.110

78		DPR016	Depression	63	0.109

79	P	PNM007	Pneumonia	68	0.108

80		LKP003	Leukoplakia	39	0.107

81	P	BPL003	Bipolar Disorder	56	0.107

82	P	INS002	in Situ Carcinoma	53	0.106

83		SLC006	Silicosis	56	0.105

84	c	ACT071	Acute Kidney Failure	60	0.105

85	c	MGR028	Migraine with or Without Aura 1	67	0.104

86	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.104

87	c	MJR024	Major Affective Disorder 9	41	0.104

88	c	MJR022	Major Affective Disorder 8	38	0.104

89		ANR040	Aneurysm	59	0.104

90	P	HRT032	Heart Disease	75	0.103

91		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.102

92		STR067	Stroke, Ischemic	81	0.102

93		DNT012	Dental Caries	53	0.100

94	P	DRR001	Diarrhea	55	0.100

95	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.100

96	P	GLM045	Glioma	63	0.100

97		GLL048	Glial Tumor	45	0.098

98		APN008	Apnea, Obstructive Sleep	64	0.098

99	P	HYP076	Hyperthyroidism	55	0.098

100		KLD004	Keloid Disorder	40	0.098

101	P	PRS040	Prostate Cancer	97	0.098

102	P	NTR004	Neutropenia	63	0.098

103	P	BNG032	Benign Mesothelioma	46	0.097

104		NRL016	Neural Tube Defects	82	0.097

105		ADL002	Adult Syndrome	70	0.097

106	P	CRN300	Coronary Heart Disease 1	63	0.097

107		DYS073	Dysphagia	50	0.096

108		SDD001	Sudden Infant Death Syndrome	61	0.096

109		ART140	Arteries, Anomalies of	52	0.095

110		MNT002	Mental Depression	58	0.095

111		OST159	Osteogenic Sarcoma	66	0.095

112		TRM010	Traumatic Brain Injury	51	0.094

113		SQM002	Squamous Cell Papilloma	46	0.094

114		LPP008	Lipoprotein Quantitative Trait Locus	62	0.093

115	c	PLM127	Pulmonary Hypertension, Primary, 3	34	0.093

116		NWB001	Newborn Respiratory Distress Syndrome	58	0.093

117		HDR002	Hidradenitis Suppurativa	55	0.092

118		LYM022	Lymphangioma	54	0.092

119		HDR003	Hidradenitis	49	0.092

120	P	RRL003	Rare Lymphatic Malformation	31	0.092

121		BCT022	Bacterial Infectious Disease	56	0.092

122	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.092

123		CNS004	Constipation	58	0.091

124		DRM006	Dermatitis	61	0.091

125	c	BSL007	Basal Cell Carcinoma	68	0.090

126		CYS001	Cystic Fibrosis	81	0.090

127	P	TRM003	Tremor	54	0.090

128		IRN002	Iron Metabolism Disease	57	0.090

129		THY029	Thyroid Carcinoma	59	0.090

130		RSP019	Respiratory Distress Syndrome in Premature Infants	58	0.089

131		BRN002	Bronchiolitis	59	0.089

132		AGN016	Aging	56	0.088

133		AMN003	Amnestic Disorder	54	0.088

134	P	MLN008	Melanoma	69	0.087

135		DFC004	Deficiency Anemia	70	0.087

136		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.087

137	P	MYC007	Myocardial Infarction	70	0.087

138	P	TRN020	Turner Syndrome	67	0.087

139		HYP056	Hypoglycemia	66	0.087

140	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.087

141	P	LTR001	Lateral Sclerosis	54	0.087

142	P	PRD008	Periodontitis	64	0.086

143	P	BLD134	Bladder Cancer	79	0.086

144		PLM031	Poliomyelitis	64	0.086

145	P	KDN017	Kidney Cancer	60	0.086

146		ATH013	Atherosclerosis Susceptibility	65	0.085

147		PRP027	Peripheral Vascular Disease	71	0.085

148		HMN044	Human Immunodeficiency Virus Type 1	71	0.085

149		CNT097	Central Hypoventilation Syndrome, Congenital	71	0.085

150		KRT009	Keratosis	51	0.085

151		HRT011	Heart Septal Defect	50	0.085

152	c	ATM006	Autoimmune Lymphoproliferative Syndrome	74	0.085

153		OST012	Osteoarthritis	78	0.085

154	P	HYP086	Hypothyroidism	69	0.084

155	P	NRP001	Neuropathy	56	0.084

156		SPN186	Spinal Cord Injury	60	0.084

157	c	RHB024	Rhabdomyosarcoma 2	67	0.084

158		LSH001	Leishmaniasis	63	0.084

159	P	KLZ004	Kala-Azar 1	41	0.084

160	c	BNG091	Benign Chronic Pemphigus	58	0.084

161	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.084

162		STM007	Stomatitis	50	0.083

163		ANT018	Anthracosis	48	0.083

164	P	HYP098	Hypereosinophilic Syndrome	67	0.083

165	P	SKN015	Skin Carcinoma	66	0.083

166		TLN003	Telangiectasis	52	0.083

167	P	INF032	Infertility	57	0.083

168		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.082

169		HMP009	Haemophilus Influenzae	43	0.082

170	P	PNM006	Pneumoconiosis	56	0.082

171		RCK004	Rickets	68	0.082

172		RSC001	Rosacea	54	0.082

173		CHL056	Cheilitis	48	0.082

174		ACT093	Actinic Cheilitis	40	0.082

175	P	GST053	Gastric Cancer	83	0.082

176	P	RCT021	Rectum Cancer	52	0.082

177	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.081

178		HDN002	Head Injury	46	0.081

179	c	SCL052	Scleroderma, Familial Progressive	61	0.081

180	P	LCT001	Lactic Acidosis	51	0.081

181		ATX019	Ataxia with Vitamin E Deficiency	42	0.081

182	P	OPN001	Open-Angle Glaucoma	49	0.080

183		AGR002	Agoraphobia	45	0.080

184		ORL012	Oral Leukoplakia	39	0.080

185		CLT003	Colitis	62	0.080

186		ORL015	Oral Squamous Cell Carcinoma	43	0.080

187		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.080

188	c	SML038	Small Cell Cancer of the Lung	65	0.079

189		CVD001	Covid-19	44	0.079

190		SKN016	Skin Disease	63	0.079

191		GST023	Gastric Ulcer	53	0.079

192		ESP021	Esophageal Cancer	90	0.079

193	c	PRC016	Pre-Eclampsia	63	0.079

194	c	GLL024	Gallbladder Disease 1	53	0.079

195	P	CRD246	Cardiovascular System Disease	57	0.078

196		PST092	Posttransplant Acute Limbic Encephalitis	29	0.078

197	c	HYP595	Hypertension, Essential	84	0.078

198		HYP066	Hyperglycemia	61	0.078

199		ORL011	Oral Cancer	60	0.077

200		MCS002	Mucositis	56	0.077

201		SYN036	Syncope	45	0.077

202		ALL006	Allergic Asthma	56	0.077

203		GST045	Gastroenteritis	59	0.077

204		CRB086	Cerebral Aneurysms	40	0.076

205		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.076

206		ALC007	Alcohol Dependence	66	0.076

207	P	INF037	Inflammatory Bowel Disease	54	0.076

208	P	VNT002	Ventricular Septal Defect	60	0.076

209		ADN011	Adenoid Cystic Carcinoma	70	0.076

210	P	OVR042	Ovarian Cancer	88	0.075

211	P	ALP008	Alopecia	54	0.075

212	P	SYR003	Syringoma	37	0.075

213	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.075

214		MDD011	Mood Disorder	62	0.074

215	P	ALZ034	Alzheimer Disease	88	0.074

216		ILS001	Ileus	51	0.074

217	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.073

218		END040	Endogenous Depression	55	0.073

219	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.073

220		RTN020	Retinal Vascular Disease	46	0.073

221		DWN001	Down Syndrome	70	0.073

222	P	HYD006	Hydrocephalus	66	0.073

223	P	TBR001	Tuberous Sclerosis	70	0.073

224		OBS037	Obesity-Hypoventilation Syndrome	46	0.073

225		ANP008	Anaplastic Oligoastrocytoma	30	0.073

226		TNP004	Tn Polyagglutination Syndrome	39	0.073

227		HYP005	Hypokalemia	55	0.073

228	P	LNG064	Lung Cancer Susceptibility 3	78	0.072

229	P	ACT105	Acute Mountain Sickness	52	0.072

230	P	SYS005	Systemic Scleroderma	68	0.072

231	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.072

232		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.072

233	c	PCH010	Pachyonychia Congenita 3	44	0.072

234		PRT013	Portal Hypertension	59	0.071

235		URL001	Urolithiasis	45	0.071

236	c	EXD008	Exudative Vitreoretinopathy 1	71	0.071

237	P	PMP001	Pemphigus	54	0.071

238	P	CND004	Candidiasis	58	0.071

239		RSP007	Respiratory Distress Syndrome, Infant	30	0.071

240		CHL014	Cholera	59	0.071

241		ANG054	Angina Pectoris	66	0.071

242		BRN028	Brain Cancer	74	0.071

243		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.070

244		BRN012	Bronchiolitis Obliterans	55	0.070

245	P	DST107	Distal Renal Tubular Acidosis	42	0.070

246	c	ACT075	Acute Myocardial Infarction	57	0.070

247	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.070

248		CHR661	Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction	48	0.070

249	c	CHR682	Chronic Bilirubin Encephalopathy	39	0.070

250		NRT001	Neurotic Disorder	53	0.069

251		BRN056	Bronchopulmonary Dysplasia	57	0.069

252		ING001	Inguinal Hernia	60	0.069

253		CRD137	Cardiogenic Shock	47	0.069

254	P	PHC003	Pheochromocytoma	71	0.069

255		ADR040	Adrenal Gland Pheochromocytoma	46	0.069

256		ATM095	Autoimmune Disease	62	0.069

257		LNT004	Lentigines	50	0.069

258	c	CNT015	Central Sleep Apnea	45	0.069

259		TRC005	Tracheal Stenosis	38	0.069

260	P	PSR002	Psoriasis	62	0.069

261		PST011	Pustulosis of Palm and Sole	52	0.069

262	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.069

263		CRB090	Cerebral Hypoxia	44	0.068

264		URT049	Urate Oxidase, Pseudogene	25	0.068

265	P	ART021	Arteriosclerosis	54	0.068

266	P	SCK005	Sickle Cell Disease	50	0.068

267		CTN007	Cutaneous Leishmaniasis	62	0.068

268		PPL001	Papillary Adenoma	44	0.068

269		INT002	Intermittent Claudication	61	0.068

270	c	PNS012	Paine Syndrome	61	0.068

271	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.067

272	P	HML002	Hemolytic Anemia	63	0.067

273	P	CTR002	Cataract	60	0.067

274	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.067

275	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.067

276	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.067

277	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.067

278	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.067

279	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.067

280	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.067

281	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.067

282	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.067

283	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.067

284	P	RTN008	Retinitis Pigmentosa	79	0.067

285		ANG005	Anogenital Venereal Wart	55	0.067

286		STT002	Status Asthmaticus	50	0.067

287		VRR004	Verrucous Carcinoma	49	0.067

288		LCH016	Lichen Sclerosus Et Atrophicus	41	0.067

289		ERY023	Erythroplakia	24	0.067

290		CHL079	Children's Interstitial Lung Disease	26	0.067

291		GTR002	Goiter	53	0.067

292	c	ART068	Aortic Aneurysm, Familial Thoracic 2	34	0.067

293	P	MCR115	Microvascular Complications of Diabetes 5	66	0.067

294	P	FBR017	Fibrosarcoma	56	0.067

295		RTN023	Retinitis	46	0.066

296		NRR001	Neuroretinitis	42	0.066

297		TRN018	Transitional Cell Carcinoma	56	0.066

298		DMP001	Dumping Syndrome	44	0.066

299		VRC005	Varicose Veins	60	0.066

300	P	PNC044	Pancreatitis	61	0.066

301		SRC014	Sarcoma	65	0.066

302		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.066

303	P	BRS044	Breast Adenocarcinoma	59	0.066

304	P	OVR082	Overgrowth Syndrome	50	0.066

305	c	ACT134	Acute Liver Failure	56	0.066

306	P	PLY019	Polyneuropathy	56	0.066

307		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.065

308		INT066	Interstitial Lung Disease	60	0.065

309	P	SCH015	Schizophrenia	74	0.065

310		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.065

311		CLN015	Colon Adenocarcinoma	65	0.065

312		MYL020	Myelomeningocele	51	0.065

313		CYN002	Cyanosis, Transient Neonatal	45	0.065

314	c	GLC092	Glaucoma, Primary Open Angle	62	0.065

315		CHR100	Chronic Ulcer of Skin	55	0.065

316	P	MLG056	Malignant Hyperthermia	67	0.065

317	c	ACT068	Acute Cystitis	63	0.065

318	c	SVR001	Severe Acute Respiratory Syndrome	62	0.065

319		MST005	Mastitis	53	0.064

320	P	PRP019	Peripheral Nervous System Disease	58	0.064

321		CNT047	Contact Dermatitis	58	0.064

322		BRN004	Brain Edema	56	0.064

323		MLR004	Malaria	81	0.063

324		ANT024	Anthrax Disease	58	0.063

325		SPN035	Spindle Cell Sarcoma	53	0.063

326		SKN019	Skin Melanoma	68	0.063

327	P	ENC004	Encephalitis	61	0.063

328		RTN017	Retinal Detachment	61	0.063

329	P	FBR031	Febrile Seizures	53	0.063

330		NPH009	Nephrolithiasis	55	0.063

331		MDS022	Mediastinitis	46	0.063

332		BWN006	Bowen's Disease	32	0.063

333	P	MYP004	Myopathy	70	0.062

334		NRM005	Neuromuscular Disease	64	0.062

335	c	ACT027	Acute Pancreatitis	60	0.062

336	P	CNR004	Cone-Rod Dystrophy 2	73	0.062

337	P	AST007	Astrocytoma	51	0.062

338	P	CHN012	Chondrosarcoma	56	0.062

339		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.062

340		NRF007	Neurofibroma	64	0.062

341		CHL004	Cholelithiasis	49	0.062

342	P	INF038	Influenza	68	0.062

343	P	ART022	Arthritis	69	0.061

344	P	MYS003	Myasthenia Gravis	68	0.061

345	c	BRN108	Branchiootic Syndrome 1	62	0.061

346		ULC004	Ulcerative Colitis	73	0.061

347	P	DBT005	Diabetes Insipidus	55	0.061

348	P	BCL017	B-Cell Lymphoma	58	0.061

349	P	GST044	Gastritis	56	0.061

350	P	SPP010	Suppressor of Tumorigenicity 3	51	0.061

351	P	MLT020	Multiple Sclerosis	72	0.060

352		PLM001	Pulmonary Tuberculosis	69	0.060

353	P	BRN022	Bronchiectasis	59	0.060

354		CHL067	Cholecystitis	57	0.060

355	P	PYL005	Pyelonephritis	56	0.060

356	P	PRM006	Primary Biliary Cirrhosis	62	0.060

357		URM002	Uremia	49	0.060

358	c	ECT041	Ectodermal Dysplasia-Syndactyly Syndrome 2	35	0.060

359	P	LKM002	Leukemia	68	0.060

360		OST003	Osteonecrosis	61	0.060

361		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.060

362		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.060

363		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.060

364		CLC006	Calcinosis	48	0.060

365	c	GRV008	Graves Disease 1	56	0.059

366		HPT004	Hepatic Coma	45	0.059

367	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.059

368		CHG001	Chagas Disease	66	0.059

369	P	SJG008	Sjogren Syndrome	61	0.059

370	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.059

371	P	ATR010	Atrial Heart Septal Defect	60	0.059

372	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.059

373		TTN003	Tetanus	65	0.059

374		SYN007	Synovitis	54	0.059

375		PLC002	Plica Syndrome	36	0.059

376		PST028	Post-Traumatic Stress Disorder	58	0.058

377	P	MTR003	Mitral Valve Stenosis	50	0.058

378		ACT084	Acute Stress Disorder	47	0.058

379	P	PRK001	Porokeratosis	55	0.058

380	P	ECT005	Ectropion	42	0.058

381		SNG003	Single Ventricular Heart	30	0.058

382		ERY069	Erythrokeratoderma ''en Cocardes''	30	0.058

383		NTR005	Nutritional Deficiency Disease	62	0.058

384		PPT005	Peptic Ulcer Disease	59	0.058

385	P	SNS001	Sensorineural Hearing Loss	60	0.057

386		SBC016	Subacute Delirium	44	0.057

387	c	ATR087	Atrial Standstill 1	75	0.057

388		CHL068	Cholestasis	61	0.057

389	P	PRC012	Pericardial Effusion	51	0.057

390		HMP001	Hemopericardium	48	0.057

391		VRS002	Virus-Associated Trichodysplasia Spinulosa	32	0.057

392		SCK003	Sickle Cell Anemia	74	0.057

393	c	MNN043	Meningioma, Familial	74	0.057

394		MNN042	Meningioma, Radiation-Induced	62	0.057

395		TRG002	Trigeminal Neuralgia	60	0.057

396		SPN021	Spinal Meningioma	50	0.057

397		SCR001	Secretory Meningioma	41	0.057

398		LYM002	Lymphoplasmacyte-Rich Meningioma	36	0.057

399	P	DMN002	Dementia	66	0.056

400		OTT002	Otitis Media	72	0.056

401	P	SLP005	Sleep Disorder	59	0.056

402	P	AMY004	Amyloidosis	70	0.055

403	P	HPT021	Hepatitis	67	0.055

404	P	DRM053	Dermatitis, Atopic	66	0.055

405		BRR014	Barrett Esophagus	65	0.055

406	P	EXN002	Exanthem	57	0.055

407		HYP815	Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome	53	0.055

408		PRP080	Peripheral Artery Disease	53	0.055

409		RDN001	Reading Disorder	40	0.055

410	P	NSP012	Nasopharyngeal Carcinoma	66	0.055

411	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.055

412		IMP005	Impotence	52	0.055

413	c	HPT073	Hepatitis C Virus	72	0.055

414		GNG013	Gingivitis	59	0.055

415		PLR007	Pleural Empyema	50	0.055

416		KRT013	Keratolytic Winter Erythema	46	0.055

417		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.055

418	P	HRP006	Herpes Simplex	65	0.054

419		LYM133	Lymphoma, Hodgkin, Classic	69	0.054

420	P	MSC005	Muscular Dystrophy	66	0.054

421		HPT019	Hepatic Encephalopathy	60	0.054

422		CHL065	Cholangiocarcinoma	68	0.053

423		INT079	Intrahepatic Cholangiocarcinoma	51	0.053

424		RYN005	Raynaud Phenomenon	47	0.053

425		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	0.053

426		NVS017	Nevus, Epidermal	68	0.053

427	P	ALP009	Alopecia Areata	60	0.053

428		AVN001	Avian Influenza	59	0.053

429		CRT013	Carotid Stenosis	50	0.053

430		ECT026	Ectopic Pregnancy	50	0.053

431		BLN010	Balanitis	37	0.053

432		IMM167	Immune Deficiency Disease	78	0.053

433	c	ATS007	Autism Spectrum Disorder	67	0.053

434	P	SCL018	Scoliosis	60	0.053

435		ARG004	Argyria	27	0.053

436	P	SRC025	Sarcoidosis 1	70	0.053

437	P	MJR001	Major Depressive Disorder	68	0.053

438		LPD008	Lipid Metabolism Disorder	62	0.053

439		NPH091	Nephrolithiasis, Calcium Oxalate	60	0.053

440		CRD223	Cardiac Arrhythmia	60	0.053

441	c	MCR113	Microvascular Complications of Diabetes 3	52	0.052

442	c	MCR120	Microvascular Complications of Diabetes 7	47	0.052

443	c	MLG068	Malignant Glioma	46	0.052

444	c	MCR130	Microvascular Complications of Diabetes 6	41	0.052

445	c	MCR133	Microvascular Complications of Diabetes 4	41	0.052

446		PRP030	Purpura	54	0.052

447		CRP002	Croup	44	0.051

448		SCK001	Sick Building Syndrome	34	0.051

449		LPT014	Leptin Deficiency or Dysfunction	74	0.051

450	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.051

451		DPH001	Diphtheria	60	0.051

452		DYS015	Dysentery	52	0.051

453	P	CLS010	Cluster Headache	42	0.051

454		MSC007	Muscle Hypertrophy	64	0.051

455	P	OBS001	Obstructive Jaundice	50	0.051

456		DNT008	Denture Stomatitis	35	0.051

457	P	URT039	Urticaria	58	0.051

458	c	LKM061	Leukemia, Acute Myeloid	84	0.050

459		END057	Endometrial Cancer	74	0.050

460		CRH001	Crohn's Disease	74	0.050

461	P	ATS364	Autism	70	0.050

462		OST017	Osteomyelitis	64	0.050

463		ENT004	Enthesopathy	49	0.050

464	c	HPT001	Hepatitis C	62	0.050

465		YLL002	Yellow Fever	61	0.050

466		VRL011	Viral Infectious Disease	61	0.050

467		PNM010	Pneumothorax, Primary Spontaneous	60	0.050

468	P	NRF002	Neurofibromatosis	56	0.050

469	c	PRD040	Periodontitis, Chronic	53	0.050

470		STT041	Stuttering	52	0.050

471		NTR046	Neutrophil Migration	50	0.050

472		RTR001	Retrograde Amnesia	44	0.050

473	P	RHM011	Rheumatoid Arthritis	80	0.050

474	P	MNN013	Meningitis	66	0.050

475	P	MYC008	Myocarditis	59	0.050

476		CHP002	Chops Syndrome	44	0.050

477		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.049

478	P	APL001	Aplastic Anemia	74	0.049

479		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.049

480	P	THR014	Thrombocytopenia	67	0.049

481		THY030	Thyroid Gland Disease	52	0.049

482		PTH003	Pathologic Nystagmus	52	0.049

483		OBS002	Obsessive-Compulsive Disorder	68	0.048

484		PLG002	Plague	63	0.048

485	P	OPT006	Optic Nerve Disease	60	0.048

486	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.048

487		CLF001	Cleft Lip	53	0.048

488		LNG031	Lung Benign Neoplasm	51	0.048

489		CRN030	Coronary Stenosis	50	0.048

490		DSS012	Disseminated Infection with Mycobacterium Avium Complex	20	0.048

491	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.048

492	P	DYS154	Dystonia	65	0.048

493	P	ECL001	Eclampsia	50	0.048

494	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.048

495	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.048

496	P	CYS018	Cystitis	59	0.048

497		BCK006	Back Pain	42	0.048

498		BTN004	Biotin Deficiency	38	0.048

499		IRR002	Irritable Bowel Syndrome	65	0.047

500		GNR004	Generalized Anxiety Disorder	56	0.047

501		MMM001	Mammary Paget's Disease	53	0.047

502	P	ACT008	Actinic Keratosis	53	0.047

503		LGN006	Legionnaire Disease	52	0.047

504		HYP781	Hypoascorbemia	51	0.047

505	P	OTS001	Otosclerosis	49	0.047

506		CVR006	Cavernous Hemangioma	49	0.047

507	P	RCR004	Recurrent Respiratory Papillomatosis	49	0.047

508		NWC001	Newcastle Disease	45	0.047

509		VLV044	Vulvar Intraepithelial Neoplasia	44	0.047

510		PYG006	Pyogenic Granuloma	41	0.047

511		SPR012	Separation Anxiety Disorder	38	0.047

512	c	PST106	Post-Cardiac Arrest Syndrome	35	0.047

513		INF057	Inflammatory Linear Verrucous Epidermal Nevus	34	0.047

514		SBG002	Subglottic Angioma	13	0.047

515	P	BRB001	Beriberi	46	0.047

516	c	MCR129	Microvascular Complications of Diabetes 1	66	0.047

517		STT001	Status Epilepticus	60	0.047

518		HLC007	Helicobacter Pylori Infection	59	0.047

519		HMS001	Hemosiderosis	54	0.047

520		PLY150	Polykaryocytosis Inducer	31	0.047

521		BNG077	Benign Idiopathic Neonatal Seizures	26	0.047

522	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.046

523	P	ART005	Arteriovenous Malformation	65	0.046

524		KRT019	Keratitis, Hereditary	65	0.046

525	P	THY023	Thymoma	65	0.046

526		PSR001	Psoriatic Arthritis	61	0.046

527		ACN002	Acanthosis Nigricans	60	0.046

528	P	LCH002	Lichen Planus	53	0.046

529	c	THY107	Thymoma, Familial	52	0.046

530		CHR466	Chronic Thromboembolic Pulmonary Hypertension	45	0.046

531		PLM101	Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis	37	0.046

532		IGR001	Ige Responsiveness, Atopic	59	0.045

533	P	GLM040	Glioma Susceptibility 1	81	0.045

534		PNC129	Pancreatic Adenocarcinoma	68	0.045

535		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.045

536		THR024	Thrombosis	57	0.045

537		GST050	Gastrointestinal System Disease	56	0.045

538		HYP060	Hyperinsulinism	54	0.045

539		NNL006	Non-Alcoholic Steatohepatitis	54	0.045

540		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	37	0.045

541		HRN029	Hearing Loss, Noise-Induced	37	0.045

542	P	PLY011	Polycystic Ovary Syndrome	56	0.045

543		CLR109	Colorectal Adenocarcinoma	51	0.045

544		GNG003	Gingival Recession	44	0.045

545		MCR011	Microinvasive Gastric Cancer	43	0.045

546		MDD018	Middle East Respiratory Syndrome	43	0.045

547		FNT004	Fainting	30	0.045

548		ENM002	Enamel Erosion	26	0.045

549		GT001	Gout	64	0.044

550		CLR108	Colorectal Adenoma	64	0.044

551	P	RHB003	Rhabdomyosarcoma	63	0.044

552		TYP007	Typhoid Fever	63	0.044

553	P	ALC033	Alcohol Use Disorder	58	0.044

554	P	TCD001	Tic Disorder	53	0.044

555		SPL018	Splenomegaly	48	0.044

556	c	MCR112	Microvascular Complications of Diabetes 2	41	0.044

557	c	RNG015	Ring Chromosome 2	26	0.044

558		TRN015	Transient Cerebral Ischemia	63	0.044

559		HYD002	Hydronephrosis	60	0.044

560		LYM027	Lymphopenia	58	0.044

561		CHK001	Chikungunya	57	0.044

562		VSC002	Vascular Dementia	57	0.044

563		MCN007	Meconium Aspiration Syndrome	55	0.044

564	P	INT068	Intestinal Disease	53	0.044

565		CRT015	Carotid Artery Occlusion	45	0.044

566		ENT001	Enterocele	39	0.044

567	c	PLM022	Pulmonary Valve Insufficiency	39	0.044

568	c	HPT003	Hepatitis a	62	0.043

569	P	VSC011	Vasculitis	62	0.043

570	P	MYP006	Myopia	55	0.043

571		NVS001	Neovascular Glaucoma	53	0.043

572		LMY002	Leiomyoma	52	0.043

573	c	DRR009	Diarrhea 6	46	0.043

574		JNT004	Joint Laxity, Short Stature, and Myopia	45	0.043

575		OVR094	Ovarian Epithelial Cancer	38	0.043

576	P	ATX030	Ataxia-Telangiectasia	82	0.042

577	c	SPN225	Spondyloarthropathy 1	73	0.042

578	P	EPL164	Epilepsy	71	0.042

579		APH002	Aphasia	57	0.042

580		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.042

581	P	CHR345	Chronic Pain	44	0.042

582		ANG020	Angiosarcoma	64	0.042

583		CLL003	Cellulitis	54	0.042

584		SVR097	Severe Cutaneous Adverse Reaction	69	0.041

585		ETN001	Eating Disorder	60	0.041

586		ERY003	Erythema Multiforme	58	0.041

587	c	BCT007	Bacterial Meningitis	55	0.041

588		TNG007	Tongue Carcinoma	51	0.041

589		ASP007	Aspiration Pneumonia	48	0.041

590		RNL077	Renal Fibrosis	47	0.041

591		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	47	0.041

592		IDP070	Idiopathic Scoliosis	42	0.041

593		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	32	0.041

594		ERY066	Erythema Multiforme Major	30	0.041

595	P	HYP055	Hypoplastic Left Heart Syndrome	63	0.041

596	c	LCL006	Localized Scleroderma	62	0.041

597	P	PRP029	Porphyria	62	0.041

598		DCB001	Decubitus Ulcer	61	0.041

599		NRL005	Neurilemmoma	60	0.041

600	c	LPM012	Lipomatosis, Multiple	60	0.041

601	P	PTN014	Patent Ductus Arteriosus 1	60	0.041

602		FDB001	Foodborne Botulism	55	0.041

603		WST005	West Nile Virus	54	0.041

604		MYM001	Myoma	54	0.041

605		ECH003	Echinococcosis	53	0.041

606		CRT016	Carotid Artery Disease	52	0.041

607		PYD002	Pyoderma	50	0.041

608		ALV007	Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins	48	0.041

609	P	OVR046	Ovarian Cyst	47	0.041

610		STT007	Steatocystoma Multiplex	46	0.041

611		SPR005	Superficial Basal Cell Carcinoma	46	0.041

612		TRT001	Teratocarcinoma	45	0.041

613	c	PRM038	Primary Agammaglobulinemia	44	0.041

614		LRY017	Laryngeal Disease	42	0.041

615		PLM005	Pleomorphic Lipoma	40	0.041

616	P	EPL003	Epulis	30	0.041

617		BLN002	Balanitis Xerotica Obliterans	29	0.041

618		MCC003	Mucocele of Salivary Gland	28	0.041

619		LKP001	Leukoplakia of Penis	25	0.041

620	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.041

621	P	LPS004	Lupus Erythematosus	61	0.041

622	P	DNG005	Dengue Virus	59	0.041

623		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.041

624		ERY051	Erythroleukemia, Familial	56	0.041

625		AMY027	Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1	54	0.041

626	P	HYP733	Hypercalciuria, Absorptive, 2	45	0.041

627	P	FBR003	Fibrous Histiocytoma	44	0.041

628		SPR126	Superior Semicircular Canal Dehiscence	40	0.041

629	c	HMG029	Hemoglobin Se Disease	39	0.041

630	c	LKM063	Leukemia, Chronic Myeloid	72	0.039

631		CNN005	Connective Tissue Disease	68	0.039

632	P	ART023	Arthropathy	62	0.039

633	P	PLY041	Polymyositis	57	0.039

634		SCH014	Schistosomiasis	57	0.039

635		ALL010	Allergic Contact Dermatitis	56	0.039

636		NPH003	Nephrocalcinosis	51	0.039

637		CRB004	Cerebral Artery Occlusion	45	0.039

638		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.039

639		ADG002	Audiogenic Seizures	25	0.039

640		APP008	Appendicitis	61	0.039

641		CHL123	Chlamydia	59	0.039

642		AYM001	Ayme-Gripp Syndrome	57	0.039

643	P	LRY044	Larynx Cancer	55	0.039

644		PRS045	Prostatic Hypertrophy	53	0.039

645	P	MNC007	Monocytic Leukemia	53	0.039

646	c	BCT013	Bacterial Pneumonia	48	0.039

647		VSM001	Vasomotor Rhinitis	38	0.039

648		CHR178	Chromosomal Triplication	35	0.039

649	P	RNL115	Renal Tubular Acidosis, Proximal	31	0.039

650		EXT062	Extracranial Carotid Artery Aneurysm	21	0.039

651	c	SVR005	Severe Pre-Eclampsia	50	0.038

652		PLP001	Pulpitis	49	0.038

653	c	ACT042	Acute Pyelonephritis	46	0.038

654		MLN073	Melanosis, Neurocutaneous	45	0.038

655	c	AST034	Asthma-Related Traits 4	28	0.038

656	P	HYP061	Hypertrophic Cardiomyopathy	70	0.037

657		MYC006	Mycosis Fungoides	66	0.037

658	P	MTR014	Motor Neuron Disease	65	0.037

659	c	JVN010	Juvenile Rheumatoid Arthritis	64	0.037

660	c	MLG084	Malignant Fibrous Histiocytoma	63	0.037

661	P	UVT001	Uveitis	57	0.037

662		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.037

663	P	RTN016	Retinal Degeneration	53	0.037

664	c	PRM092	Primary Lateral Sclerosis, Adult, 1	53	0.037

665	P	MSC003	Muscular Atrophy	52	0.037

666		BHR001	Behr Syndrome	51	0.037

667		PLC008	Placenta Disease	50	0.037

668	P	MYT002	Myotonic Dystrophy	49	0.037

669		VCC001	Vaccinia	49	0.037

670		SXL003	Sexual Disorder	47	0.037

671		MXD026	Mixed Glioma	45	0.037

672		ACT003	Acute Kidney Tubular Necrosis	45	0.037

673	P	PRC031	Preeclampsia/eclampsia 1	38	0.037

674	c	RNG019	Ring Chromosome 3	22	0.037

675	P	MYC084	Mycobacterium Tuberculosis 1	68	0.037

676	c	DPH024	Diaphragmatic Hernia, Congenital	63	0.037

677		GST033	Gestational Diabetes	61	0.037

678	P	SYP003	Syphilis	58	0.037

679		GLS018	Glass Syndrome	57	0.037

680	c	VSC019	Vesicoureteral Reflux 1	57	0.037

681	c	BSL024	Basal Cell Carcinoma 1	56	0.037

682	P	MLN007	Male Infertility	55	0.037

683	P	VNS003	Venous Insufficiency	55	0.037

684		PRC013	Pericarditis	54	0.037

685		MTN003	Motion Sickness	53	0.037

686	P	PTS002	Ptosis	53	0.037

687		PRS021	Prostatic Adenoma	51	0.037

688		ACH005	Achalasia	51	0.037

689		RSP006	Respiratory System Disease	50	0.037

690		SYS003	Systolic Heart Failure	49	0.037

691		PRS129	Prostatic Hyperplasia, Benign	49	0.037

692		SCL003	Social Phobia	48	0.037

693		PYL006	Pyloric Stenosis	48	0.037

694		RSP021	Respiratory Allergy	45	0.037

695		URT010	Ureteral Obstruction	45	0.037

696		CRS005	Crest Syndrome	43	0.037

697	P	HYP009	Hypertrophic Pyloric Stenosis	41	0.037

698	c	ACT004	Acute Diarrhea	39	0.037

699		CHN011	Chondromalacia	38	0.037

700		MYC014	Mycobacterium Chelonae	31	0.037

701	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.035

702		INS024	Insulin-Like Growth Factor I	79	0.035

703		MYL005	Myelofibrosis	70	0.035

704	P	OCL013	Oculodentodigital Dysplasia	69	0.035

705	P	SPN046	Spinal Muscular Atrophy	62	0.035

706	P	END033	Endocarditis	57	0.035

707		INT303	Intracranial Hypertension, Idiopathic	57	0.035

708		HMP005	Hemiplegia	55	0.035

709		OST016	Osteochondrosis	53	0.035

710	P	HMR003	Hemorrhagic Disease	53	0.035

711	P	RTN018	Retinal Disease	53	0.035

712		PRP016	Paraplegia	52	0.035

713	P	TRT010	Teratoma	52	0.035

714		CND002	Conduct Disorder	51	0.035

715		PRT029	Parathyroid Adenoma	50	0.035

716		PPL021	Papilledema	49	0.035

717		CLN045	Colonic Benign Neoplasm	46	0.035

718		PLR022	Pleural Disease	45	0.035

719		MYX004	Myxedema	43	0.035

720	c	ADN012	Adenocarcinoma in Situ	42	0.035

721		PRS063	Paresthesia	41	0.035

722		PRM020	Premenstrual Tension	40	0.035

723	P	LRY019	Laryngitis	52	0.034

724		HMN016	Hemangioendothelioma	34	0.034

725		BSL036	Basal Cell Nevus Syndrome	73	0.034

726	P	MST009	Mastocytosis	64	0.034

727		PTN001	Patent Foramen Ovale	60	0.034

728	P	GLL020	Gallbladder Disease	57	0.034

729		CMM005	Common Cold	57	0.034

730		MTH009	Mouth Disease	56	0.034

731		ORL005	Oral Candidiasis	56	0.034

732		PLV003	Pelvic Inflammatory Disease	55	0.034

733	P	DXT004	Dextro-Looped Transposition of the Great Arteries	54	0.034

734	P	NLD001	Nail Disease	54	0.034

735	c	PSR017	Psoriasis 2	53	0.034

736	c	PSR023	Psoriasis 1	52	0.034

737		FML037	Female Breast Cancer	52	0.034

738		PRV004	Periventricular Leukomalacia	52	0.034

739		FDL002	Food Allergy	51	0.034

740	c	PYR010	Peyronie's Disease	50	0.034

741		BLS002	Blastomycosis	50	0.034

742		VGN020	Vaginal Disease	49	0.034

743	P	MTC133	Mitochondrial Myopathy	49	0.034

744		PRN014	Paronychia	49	0.034

745	c	PSR032	Psoriasis 11	47	0.034

746		VGN019	Vaginal Discharge	46	0.034

747		CRB008	Cerebral Atherosclerosis	44	0.034

748		ANL017	Anal Squamous Cell Carcinoma	44	0.034

749		FBR054	Fibroma	44	0.034

750		MGS001	Megaesophagus	43	0.034

751	c	PSR028	Psoriasis 7	42	0.034

752	c	PRK082	Porokeratosis 1, Multiple Types	41	0.034

753	c	PSR018	Psoriasis 13	41	0.034

754		HYP344	Hyperthyroidism, Familial Gestational	39	0.034

755		DSS010	Dissociative Disorder	39	0.034

756		ANG016	Angiokeratoma	38	0.034

757		ACN010	Acanthoma	38	0.034

758		KLD003	Keloid Formation	38	0.034

759		LCR004	La Crosse Encephalitis	37	0.034

760		EPD070	Epidermoid Cysts	37	0.034

761		CHL013	Cholecystolithiasis	37	0.034

762		BWN003	Bowenoid Papulosis	34	0.034

763	P	CLR001	Clear Cell Acanthoma	34	0.034

764		ANG007	Angiokeratoma Circumscriptum	34	0.034

765		DRM003	Dermatosis Papulosa Nigra	33	0.034

766		CMM003	Common Wart	32	0.034

767		HDR001	Hidrocystoma	31	0.034

768		ELS002	Elastosis Perforans Serpiginosa	30	0.034

769		LRY027	Laryngeal Papillomatosis	23	0.034

770	P	SPN237	Spina Bifida Aperta	20	0.034

771		APN007	Apnea, Central Sleep	18	0.034

772		RSP020	Respiratory Underresponsiveness to Hypoxia and Hypercapnia	9	0.034

773		KPS004	Kaposi Sarcoma	75	0.033

774		MYL009	Myelodysplastic Syndrome	70	0.033

775		MLT157	Multiple System Atrophy 1	70	0.033

776	P	CHR012	Chronic Granulomatous Disease	67	0.033

777	c	DBT099	Diabetes Mellitus, Type I	65	0.033

778	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.033

779	P	ORT004	Orthostatic Intolerance	62	0.033

780	P	DRM010	Dermatomyositis	61	0.033

781	c	HPT016	Hepatitis B	59	0.033

782	c	HYD046	Hydatidiform Mole, Recurrent, 1	59	0.033

783	P	GLM007	Glomerulonephritis	57	0.033

784		DSS009	Disseminated Intravascular Coagulation	57	0.033

785	P	MYS005	Myositis	56	0.033

786		INT007	Intermediate Coronary Syndrome	55	0.033

787		VGN023	Vaginitis	54	0.033

788		INT051	Intussusception	53	0.033

789		DRM011	Dermatophytosis	52	0.033

790		DYS009	Dysthymic Disorder	49	0.033

791		QDR001	Quadriplegia	48	0.033

792		NRN001	Neuroendocrine Carcinoma	47	0.033

793		KRT002	Keratomalacia	47	0.033

794		EXS001	Exostosis	46	0.033

795		GST010	Gestational Trophoblastic Neoplasm	46	0.033

796	P	MYC033	Myoclonus	46	0.033

797	P	CRB088	Cerebral Atrophy	37	0.033

798		GRM010	Germ Cells Tumors	34	0.033

799		INF118	Inflammatory Myopathy with Abundant Macrophages	28	0.033

800		MST020	Mast Cell Activation Syndrome	26	0.033

801		LTH043	Lithium Transport	18	0.033

802	P	RTT002	Rett Syndrome	80	0.031

803		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.031

804	P	FML011	Familial Adenomatous Polyposis	72	0.031

805	c	HMP029	Hemophilia a	67	0.031

806	P	CNJ013	Conjunctivitis	65	0.031

807	c	ART101	Aortic Valve Disease 2	65	0.031

808		DSM004	Desmoid Tumor	64	0.031

809	c	PLY162	Polyposis Syndrome, Hereditary Mixed, 1	63	0.031

810		BDD001	Budd-Chiari Syndrome	63	0.031

811		BLD131	Bladder Urothelial Carcinoma	62	0.031

812		BLM002	Bulimia Nervosa	57	0.031

813	P	LKD017	Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism	57	0.031

814	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	55	0.031

815		TRC109	Tracheoesophageal Fistula with or Without Esophageal Atresia	55	0.031

816		URN010	Urinary Tract Obstruction	55	0.031

817		CLF004	Cleft Lip/palate	54	0.031

818		GNT003	Genital Herpes	54	0.031

819		THR013	Thoracic Outlet Syndrome	54	0.031

820		AMN001	Amenorrhea	54	0.031

821		RHM028	Rheumatic Heart Disease	53	0.031

822		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.031

823	P	HMP007	Hemophilia	51	0.031

824		ESP002	Esophageal Varix	51	0.031

825		NRM004	Neuroma	51	0.031

826	P	FNC004	Fanconi Syndrome	50	0.031

827		BRX001	Bruxism	50	0.031

828		HPT014	Hepatorenal Syndrome	50	0.031

829		CHL122	Cholesteatoma of Middle Ear	50	0.031

830		HMG002	Hemoglobinuria	50	0.031

831		CHL061	Childhood Leukemia	48	0.031

832		INT017	Intestinal Schistosomiasis	48	0.031

833		TBR011	Tuberculous Meningitis	48	0.031

834		KRT008	Keratopathy	47	0.031

835		CNT033	Central Nervous System Cancer	47	0.031

836	P	PRD037	Periodontal Ehlers-Danlos Syndrome	45	0.031

837		ISC015	Ischemic Colitis	44	0.031

838		TNG009	Tongue Squamous Cell Carcinoma	44	0.031

839	P	CRN024	Corneal Disease	44	0.031

840	P	MYG005	Myoglobinuria	44	0.031

841		OST115	Osteonecrosis of the Jaw	40	0.031

842	P	FNC034	Fanconi Renotubular Syndrome 2	40	0.031

843		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.031

844	P	DNT007	Dentin Sensitivity	36	0.031

845		ABD010	Abdominal Wall Defect	36	0.031

846		TBL029	Tubulin, Beta	28	0.031

847	P	HRM021	Hair Morphology 2	22	0.031

848	c	INF071	Inflammatory Bowel Disease 1	67	0.030

849	P	BLD062	Bile Duct Cancer	67	0.030

850		APH001	Aphthous Stomatitis	57	0.030

851		PHR003	Pharyngitis	57	0.030

852		LST001	Listeriosis	56	0.030

853	P	OVR049	Ovarian Disease	52	0.030

854	c	HRD202	Hereditary Lymphedema I	50	0.030

855	c	HYD064	Hydrocephalus, Congenital, 1	48	0.030

856		TSY002	Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations	45	0.030

857		SCR011	Scrapie	39	0.030

858	c	NRF024	Neurofibromatosis, Type I	77	0.028

859		ADR007	Adrenoleukodystrophy	75	0.028

860	P	TTR001	Tetralogy of Fallot	70	0.028

861		ACR008	Acrocallosal Syndrome	69	0.028

862	P	MPL001	Maple Syrup Urine Disease	69	0.028

863		FCT007	Factor Vii Deficiency	67	0.028

864	P	PRP003	Porphyria Cutanea Tarda	67	0.028

865		LNG039	Lung Squamous Cell Carcinoma	66	0.028

866	P	HRS035	Hirschsprung Disease 1	65	0.028

867	P	PSD087	Pseudoxanthoma Elasticum	65	0.028

868		ART002	Arts Syndrome	64	0.028

869		BLL006	Bullous Pemphigoid	62	0.028

870	P	ART067	Aortic Aneurysm, Familial Thoracic 1	61	0.028

871		CHC001	Chickenpox	60	0.028

872		DRR014	Darier-White Disease	60	0.028

873	P	PRD006	Prader-Willi Syndrome	59	0.028

874	P	GLL022	Guillain-Barre Syndrome	59	0.028

875		KRT071	Keratosis, Seborrheic	58	0.028

876	P	INT070	Intestinal Obstruction	58	0.028

877		RBS001	Rabies	58	0.028

878	P	MTR012	Mitral Valve Disease	58	0.028

879		EXT034	Extrinsic Allergic Alveolitis	58	0.028

880	P	PNL012	Penile Cancer	56	0.028

881		PRS047	Prostatitis	56	0.028

882		HPT022	Hepatoblastoma	56	0.028

883		VSC003	Visceral Leishmaniasis	55	0.028

884	P	SLM003	Salmonellosis	55	0.028

885		GLS001	Gliosarcoma	54	0.028

886		HMN009	Hemangioblastoma	54	0.028

887		BRN014	Bronchopneumonia	54	0.028

888		GST009	Gastroschisis	53	0.028

889	P	END047	Endophthalmitis	53	0.028

890		HYP063	Hypersplenism	53	0.028

891	c	CRD147	Cardiomyopathy, Familial Hypertrophic, 20	53	0.028

892		TRC003	Trichomoniasis	53	0.028

893	P	NRC002	Narcolepsy	52	0.028

894		SKN013	Skin Benign Neoplasm	51	0.028

895		AZS001	Azoospermia	50	0.028

896		RBF001	Riboflavin Deficiency	49	0.028

897		KRT001	Keratoconjunctivitis Sicca	49	0.028

898		DFF035	Diffuse Cutaneous Systemic Sclerosis	49	0.028

899		HST010	Histiocytosis	48	0.028

900		RYN001	Raynaud Disease	48	0.028

901		HPR003	Heparin-Induced Thrombocytopenia	48	0.028

902		ADN009	Adenosquamous Carcinoma	47	0.028

903		CHR031	Chromoblastomycosis	47	0.028

904		NDL007	Nodular Goiter	47	0.028

905	c	CNG216	Congenital Hydrocephalus	47	0.028

906		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.028

907		HYP082	Hypopharynx Cancer	47	0.028

908		CMP002	Campylobacteriosis	46	0.028

909		ANL022	Anal Fistula	46	0.028

910		ANG018	Angiomyolipoma	46	0.028

911		EXS017	Exstrophy of Bladder	45	0.028

912		ASP026	Asplenia, Isolated Congenital	44	0.028

913		DBT008	Diabetic Angiopathy	44	0.028

914		ANK020	Ankyloglossia with or Without Tooth Anomalies	44	0.028

915		SPN032	Spindle Cell Carcinoma	44	0.028

916		DVR002	Diverticulitis	43	0.028

917		ENC005	Encephalomalacia	43	0.028

918		RTC009	Reticulum Cell Sarcoma	43	0.028

919	c	PRG001	Progressive Muscular Atrophy	42	0.028

920		CRB025	Carbohydrate Metabolic Disorder	41	0.028

921	P	CYS017	Cystic Teratoma	41	0.028

922		ELP001	Elephantiasis	41	0.028

923		LCR013	Lacrimal Duct Defect	41	0.028

924	P	ECT045	Ectodermal Dysplasia-Syndactyly Syndrome 1	39	0.028

925	P	DYS021	Dysautonomia	39	0.028

926		RTN002	Retinal Perforation	38	0.028

927		MLN011	Malonyl-Coa Decarboxylase Deficiency	38	0.028

928		GLB021	Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies	38	0.028

929	c	CHR098	Chronic Pyelonephritis	38	0.028

930		SHW001	Shwartzman Phenomenon	37	0.028

931		CRD016	Cardiac Rupture	37	0.028

932		HMM004	Hamamy Syndrome	37	0.028

933		CNT057	Central Centrifugal Cicatricial Alopecia	36	0.028

934		SLL001	Sialolithiasis	35	0.028

935	c	LKM005	Leukemia, T-Cell, Chronic	34	0.028

936		PTL009	Patella, Chondromalacia of	33	0.028

937	P	VSC018	Visceral Steatosis	33	0.028

938		INV005	Inverted Follicular Keratosis	32	0.028

939		BLP006	Blepharoconjunctivitis	31	0.028

940		PLR005	Pleuropneumonia	31	0.028

941		CRT069	Cortical Malformations, Occipital	30	0.028

942		LMN005	Lmna-Related Cardiocutaneous Progeria Syndrome	30	0.028

943		MLG163	Malignant Tumor of Penis	29	0.028

944		MYC088	Mycobacterium Avium Complex Infections	29	0.028

945		CYT018	Cytochrome P450 2d6 Variant	27	0.028

946		CHR603	Chronic Enteropathy Associated with Slco2a1 Gene	25	0.028

947		EPL050	Epilepsy, Partial, with Pericentral Spikes	25	0.028

948		CMB039	Combined Pulmonary Fibrosis-Emphysema Syndrome	20	0.028

949	c	ART115	Aortic Valve Disease 1	75	0.024

950		ACR007	Acromegaly	71	0.024

951		PTZ001	Peutz-Jeghers Syndrome	70	0.024

952	P	CRN037	Craniosynostosis	68	0.024

953	P	CWD010	Cowden Syndrome	67	0.024

954		STH001	Saethre-Chotzen Syndrome	67	0.024

955	c	NRP054	Neuropathy, Hereditary Sensory and Autonomic, Type Iii	67	0.024

956	P	FML364	Familial Thoracic Aortic Aneurysm and Aortic Dissection	66	0.024

957		BRK001	Brooke-Spiegler Syndrome	64	0.024

958	P	FRD001	Friedreich Ataxia	64	0.024

959		TKY002	Takayasu Arteritis	62	0.024

960	c	ANM038	Anemia, Autoimmune Hemolytic	62	0.024

961		SCH078	Schimmelpenning-Feuerstein-Mims Syndrome	62	0.024

962	P	INT143	Interstitial Cystitis	61	0.024

963		CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	60	0.024

964		KLP010	Klippel-Trenaunay-Weber Syndrome	59	0.024

965	P	HMN036	Hemangiopericytoma, Malignant	59	0.024

966		PLM026	Pilomatrixoma	58	0.024

967		PMP006	Pemphigus Vulgaris, Familial	57	0.024

968	P	PLV020	Pelvic Organ Prolapse	57	0.024

969	P	MYM013	Moyamoya Disease 1	57	0.024

970		TNS005	Tonsillitis	57	0.024

971		CYT008	Cytomegalovirus Infection	57	0.024

972		PLM102	Palmoplantar Keratoderma, Epidermolytic	56	0.024

973		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.024

974		ACS001	Acoustic Neuroma	56	0.024

975		PTS001	Patau Syndrome	55	0.024

976		NRG002	Neurogenic Bladder	55	0.024

977		CRC006	Carcinoid Syndrome	55	0.024

978		MYP159	Myopathy, Proximal, with Ophthalmoplegia	55	0.024

979		PYD001	Pyoderma Gangrenosum	54	0.024

980		DBT010	Diabetic Neuropathy	54	0.024

981		SLP001	Sleeping Sickness	54	0.024

982		FRZ001	Frozen Shoulder	53	0.024

983		PLM136	Palmoplantar Keratoderma, Nonepidermolytic	53	0.024

984		KRT006	Keratoconjunctivitis	53	0.024

985		ERD001	Erdheim-Chester Disease	53	0.024

986		ALC009	Alcoholic Liver Cirrhosis	53	0.024

987		TRC008	Trachoma	53	0.024

988		OVR059	Ovary Adenocarcinoma	53	0.024

989		ANG046	Angioimmunoblastic T-Cell Lymphoma	52	0.024

990		ART074	Aortic Dissection	52	0.024

991	P	MGR003	Migraine with Aura	52	0.024

992	P	CPL006	Capillary Hemangioma	51	0.024

993	P	HRD012	Hereditary Elliptocytosis	51	0.024

994		CHR005	Chorioamnionitis	51	0.024

995		LPD016	Lipoid Proteinosis of Urbach and Wiethe	50	0.024

996	P	OMP004	Omphalocele	50	0.024

997		BLL004	Bullous Keratopathy	49	0.024

998		VLV011	Vulvovaginal Candidiasis	49	0.024

999		PCT003	Pectus Excavatum	49	0.024

1000		ART017	Aortic Disease	49	0.024

1001		GST049	Gastrointestinal System Cancer	49	0.024

1002		CHN065	Choanal Atresia, Posterior	49	0.024

1003	P	ALP061	Alopecia, Androgenetic, 1	49	0.024

1004		NRL018	Neural Tube Defects, Folate-Sensitive	48	0.024

1005		BRS064	Bursitis	48	0.024

1006		MNC006	Monoclonal Gammopathy of Uncertain Significance	48	0.024

1007	P	GND004	Gonadal Dysgenesis	48	0.024

1008	P	UTR058	Uterine Anomalies	47	0.024

1009		LRY029	Laryngomalacia	47	0.024

1010		CLN019	Colonic Disease	47	0.024

1011	P	CRN028	Corneal Ulcer	47	0.024

1012		CRD001	Cardiac Tamponade	47	0.024

1013	P	RNL015	Renal Hypertension	47	0.024

1014		CRN027	Corneal Neovascularization	47	0.024

1015		LYM012	Lymphoplasmacytic Lymphoma	47	0.024

1016		GST071	Gastrointestinal Carcinoma	47	0.024

1017		ASP004	Asphyxia Neonatorum	46	0.024

1018	c	ACT076	Acute Myocarditis	46	0.024

1019		FCL012	Facial Paralysis	46	0.024

1020		PLL012	Pollen Allergy	46	0.024

1021		AND014	Androgenic Alopecia	46	0.024

1022		MGC001	Megacolon	46	0.024

1023		VLV036	Vulvar Disease	46	0.024

1024		RTR008	Root Resorption	45	0.024

1025	c	NLD009	Nail Disorder, Nonsyndromic Congenital, 1	45	0.024

1026		PPL018	Papillary Adenocarcinoma	45	0.024

1027		DST006	Diastolic Heart Failure	45	0.024

1028	P	CMM008	Communicating Hydrocephalus	45	0.024

1029		KDN015	Kidney Angiomyolipoma	45	0.024

1030		MCR037	Macroglossia	45	0.024

1031	P	DCR003	Dacryoadenitis	45	0.024

1032		TWN001	Twin-to-Twin Transfusion Syndrome	45	0.024

1033		BLC012	Bile Acid Malabsorption, Primary	45	0.024

1034		INF058	Inflammatory Myofibroblastic Tumor	45	0.024

1035	c	JVN003	Juvenile Xanthogranuloma	44	0.024

1036		HPT082	Hepatic Adenomas, Familial	44	0.024

1037		MTR010	Mature Teratoma	44	0.024

1038	P	PRM001	Primary Cutaneous Amyloidosis	44	0.024

1039		CLN044	Colon Adenoma	44	0.024

1040	P	PLM085	Pulmonary Hemosiderosis	44	0.024

1041		CRD178	Cardiac Conduction Disease with or Without Dilated Cardiomyopathy	43	0.024

1042	c	HYP575	Hypotrichosis 7	43	0.024

1043		NDL009	Nodular Basal Cell Carcinoma	43	0.024

1044		ANG011	Angiodysplasia	43	0.024

1045	P	HRD018	Hair Disease	43	0.024

1046		MCR103	Microtia	43	0.024

1047		DSC009	Discoid Lupus Erythematosus	42	0.024

1048	P	GRN010	Granular Cell Tumor	42	0.024

1049		RNL097	Renal Artery Disease	42	0.024

1050	P	DWL001	Dowling-Degos Disease	42	0.024

1051	P	HYP087	Hypotrichosis	42	0.024

1052		ARC002	Arachnoiditis	42	0.024

1053		FBR019	Fibromatosis	41	0.024

1054		GST020	Gastric Antral Vascular Ectasia	41	0.024

1055	P	CHR342	Chiari Malformation	41	0.024

1056		LYM010	Lymph Node Tuberculosis	41	0.024

1057		DFF003	Diffuse Scleroderma	41	0.024

1058		PHB003	Phobia, Specific	41	0.024

1059		VST004	Vestibular Disease	41	0.024

1060	c	FBR072	Febrile Seizures, Familial, 11	41	0.024

1061	c	AMY060	Amyloidosis, Primary Localized Cutaneous, 1	41	0.024

1062		CNS002	Constrictive Pericarditis	40	0.024

1063		CLD014	Cole Disease	40	0.024

1064	c	PLM150	Pulmonary Alveolar Proteinosis, Acquired	40	0.024

1065		HYP540	Hypertension, Diastolic	40	0.024

1066		ART008	Arteriosclerosis Obliterans	40	0.024

1067		WST002	Western Equine Encephalitis	40	0.024

1068		SCR015	Scarlet Fever	39	0.024

1069		NVS015	Nevus Comedonicus	39	0.024

1070		CTN004	Cutaneous Fibrous Histiocytoma	39	0.024

1071		END011	Endometriosis of Ovary	39	0.024

1072		MLT016	Multicentric Reticulohistiocytosis	39	0.024

1073		CHL070	Cholesterol Embolism	39	0.024

1074		ADP007	Adie Pupil	39	0.024

1075		NM001	Noma	38	0.024

1076		OCH001	Ochronosis	38	0.024

1077		URT004	Urethral Syndrome	38	0.024

1078		TRC026	Tracheal Disease	38	0.024

1079		NCR002	Necrobiosis Lipoidica	38	0.024

1080	c	ELL005	Elliptocytosis 2	38	0.024

1081		BLR004	Biliary Dyskinesia	38	0.024

1082	P	SLP003	Salpingitis	38	0.024

1083		STL001	St. Louis Encephalitis	37	0.024

1084