Search results for Nicotinamide

838 hits were found for Nicotinamide

#	Family	MCID	Name	MIFTS	Score
1		HYP066	Hyperglycemia	61	0.180

2	P	SKN015	Skin Carcinoma	66	0.144

3	c	NRF023	Neurofibromatosis, Type Ii	80	0.127

4		FTT001	Fatty Liver Disease	61	0.118

5		CRB004	Cerebral Artery Occlusion	45	0.118

6	c	DBT099	Diabetes Mellitus, Type I	65	0.116

7		AGN016	Aging	56	0.116

8	P	DBT009	Diabetes Mellitus	64	0.111

9		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.108

10		DPH001	Diphtheria	60	0.108

11		GLC003	Glucose Intolerance	54	0.108

12	P	KDN018	Kidney Disease	72	0.106

13	P	LVR013	Liver Disease	68	0.106

14	c	MCR113	Microvascular Complications of Diabetes 3	52	0.106

15	c	MCR120	Microvascular Complications of Diabetes 7	47	0.106

16	P	PLL002	Pellagra	46	0.106

17	c	MCR130	Microvascular Complications of Diabetes 6	41	0.106

18	c	MCR133	Microvascular Complications of Diabetes 4	41	0.106

19		BRN071	Brain Injury	49	0.103

20	P	BLD134	Bladder Cancer	79	0.100

21	c	CHR684	Chronic Kidney Disease	70	0.100

22	P	NRP001	Neuropathy	56	0.100

23		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.100

24		ISC004	Ischemia	58	0.097

25		HYP025	Hyperphosphatemia	48	0.097

26	P	ALZ034	Alzheimer Disease	88	0.094

27	P	NRB001	Neuroblastoma	72	0.091

28	P	MLN008	Melanoma	69	0.091

29		HYP056	Hypoglycemia	66	0.091

30		BLL006	Bullous Pemphigoid	62	0.091

31		48X005	48,xyyy	39	0.091

32	P	CHR012	Chronic Granulomatous Disease	67	0.088

33		LPD008	Lipid Metabolism Disorder	62	0.088

34	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.085

35		GLB015	Glioblastoma Multiforme	75	0.085

36	c	PRC016	Pre-Eclampsia	63	0.085

37	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.085

38		HYP266	Hypoxia	57	0.085

39	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.085

40		TRM010	Traumatic Brain Injury	51	0.085

41		WLL004	Wallerian Degeneration	39	0.085

42	P	PRP019	Peripheral Nervous System Disease	58	0.082

43		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.082

44	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.078

45	P	PRK057	Parkinson Disease, Late-Onset	78	0.078

46	c	ATR087	Atrial Standstill 1	75	0.078

47	P	MYP004	Myopathy	70	0.078

48	P	DRM053	Dermatitis, Atopic	66	0.078

49		SKN016	Skin Disease	63	0.078

50		SQM006	Squamous Cell Carcinoma	60	0.078

51		ADN018	Adenoma	59	0.078

52	P	CRD246	Cardiovascular System Disease	57	0.078

53	P	LNG032	Lung Cancer	98	0.075

54	P	HNT016	Huntington Disease	72	0.075

55	P	VSC007	Vascular Disease	63	0.075

56	P	PSR002	Psoriasis	62	0.075

57	P	PMP001	Pemphigus	54	0.075

58		PST011	Pustulosis of Palm and Sole	52	0.075

59		END086	End Stage Renal Disease	51	0.075

60		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.075

61		HMP009	Haemophilus Influenzae	43	0.075

62	P	CLR023	Colorectal Cancer	99	0.071

63	c	HYP595	Hypertension, Essential	84	0.071

64	P	HRT032	Heart Disease	75	0.071

65		ATH013	Atherosclerosis Susceptibility	65	0.071

66	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.071

67		ATM095	Autoimmune Disease	62	0.071

68	P	OVR042	Ovarian Cancer	88	0.067

69		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.067

70	P	SCH015	Schizophrenia	74	0.067

71		CNG034	Congestive Heart Failure	69	0.067

72	c	SML038	Small Cell Cancer of the Lung	65	0.067

73	P	ADN016	Adenocarcinoma	64	0.067

74	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.067

75		DRM006	Dermatitis	61	0.067

76	P	ENC018	Encephalopathy	61	0.067

77		THY029	Thyroid Carcinoma	59	0.067

78		VSL002	Visual Epilepsy	59	0.067

79		FML063	Familial Glucocorticoid Deficiency	58	0.067

80	P	MTC069	Mitochondrial Disorders	56	0.067

81	P	SZR006	Seizure Disorder	56	0.067

82		HYP060	Hyperinsulinism	54	0.067

83		DBT010	Diabetic Neuropathy	54	0.067

84		NNL006	Non-Alcoholic Steatohepatitis	54	0.067

85		CYT002	Cytokine Deficiency	42	0.067

86		ANX004	Anoxia	40	0.067

87	P	HPT023	Hepatocellular Carcinoma	100	0.062

88		STR067	Stroke, Ischemic	81	0.062

89	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.062

90	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.062

91	P	MYC084	Mycobacterium Tuberculosis 1	68	0.062

92	P	DMN002	Dementia	66	0.062

93		KHL003	Kohlschutter-Tonz Syndrome	65	0.062

94	c	SVR001	Severe Acute Respiratory Syndrome	62	0.062

95		ALL026	Allergic Hypersensitivity Disease	62	0.062

96		CHL014	Cholera	59	0.062

97		RSC001	Rosacea	54	0.062

98	P	LCT001	Lactic Acidosis	51	0.062

99	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	46	0.062

100		ORL015	Oral Squamous Cell Carcinoma	43	0.062

101	c	DLT002	Dilated Cardiomyopathy	79	0.058

102	P	MYC007	Myocardial Infarction	70	0.058

103	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.058

104		ART016	Aortic Aneurysm	69	0.058

105	c	BSL007	Basal Cell Carcinoma	68	0.058

106		SKN019	Skin Melanoma	68	0.058

107		RCK004	Rickets	68	0.058

108	P	THR014	Thrombocytopenia	67	0.058

109	P	NRV007	Nervous System Disease	66	0.058

110	P	FRD001	Friedreich Ataxia	64	0.058

111		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.058

112		INS001	Insulinoma	60	0.058

113	P	MYC008	Myocarditis	59	0.058

114		ART140	Arteries, Anomalies of	52	0.058

115	P	ECL001	Eclampsia	50	0.058

116	P	SCK005	Sickle Cell Disease	50	0.058

117	P	PRC031	Preeclampsia/eclampsia 1	38	0.058

118	P	BRS047	Breast Cancer	97	0.053

119	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.053

120	c	SYS001	Systemic Lupus Erythematosus	86	0.053

121	P	PNC035	Pancreatic Cancer	84	0.053

122	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.053

123	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.053

124		DFC004	Deficiency Anemia	70	0.053

125	P	PLM037	Pulmonary Hypertension	67	0.053

126		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.053

127		PRT037	Pertussis	65	0.053

128	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.053

129		LPP008	Lipoprotein Quantitative Trait Locus	62	0.053

130		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	61	0.053

131	P	LPS004	Lupus Erythematosus	61	0.053

132	P	BCL017	B-Cell Lymphoma	58	0.053

133	c	DWL002	Dowling-Degos Disease 1	58	0.053

134	P	FBR017	Fibrosarcoma	56	0.053

135	P	DRR001	Diarrhea	55	0.053

136	P	GRV001	Graves' Disease	55	0.053

137	P	INF037	Inflammatory Bowel Disease	54	0.053

138	c	PSR017	Psoriasis 2	53	0.053

139	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.053

140	c	PSR023	Psoriasis 1	52	0.053

141	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.053

142	P	MTC133	Mitochondrial Myopathy	49	0.053

143		MTC005	Mitochondrial Metabolism Disease	49	0.053

144	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.053

145	c	PSR032	Psoriasis 11	47	0.053

146	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.053

147	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.053

148	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.053

149	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.053

150	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.053

151	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.053

152	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.053

153	c	PSR028	Psoriasis 7	42	0.053

154	c	PSR018	Psoriasis 13	41	0.053

155		PRP075	Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss	37	0.053

156		MTC023	Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes	34	0.053

157	P	PRS040	Prostate Cancer	97	0.047

158	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.047

159	P	GST053	Gastric Cancer	83	0.047

160		CRV035	Cervical Cancer	76	0.047

161	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.047

162		ULC004	Ulcerative Colitis	73	0.047

163		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.047

164	c	LKM063	Leukemia, Chronic Myeloid	72	0.047

165	P	SLP006	Sleep Apnea	69	0.047

166	P	LYM118	Lymphoma	68	0.047

167		CRB039	Cerebrovascular Disease	67	0.047

168		ACR006	Aceruloplasminemia	65	0.047

169		MSC007	Muscle Hypertrophy	64	0.047

170	P	HYP069	Hyperparathyroidism	63	0.047

171		NTR005	Nutritional Deficiency Disease	62	0.047

172		CHR066	Chronic Fatigue Syndrome	61	0.047

173		GST033	Gestational Diabetes	61	0.047

174	P	MYL006	Myeloid Leukemia	60	0.047

175		SPN186	Spinal Cord Injury	60	0.047

176	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.047

177		ORL011	Oral Cancer	60	0.047

178	c	ACT071	Acute Kidney Failure	60	0.047

179		ANR040	Aneurysm	59	0.047

180		ERY029	Erythermalgia, Primary	58	0.047

181		CNS004	Constipation	58	0.047

182	P	INF032	Infertility	57	0.047

183	P	EXN002	Exanthem	57	0.047

184	P	HDC001	Headache	57	0.047

185	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.047

186		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	56	0.047

187	P	HYP076	Hyperthyroidism	55	0.047

188	P	LRY044	Larynx Cancer	55	0.047

189		SNS003	Sensory Peripheral Neuropathy	54	0.047

190	P	CTN003	Cutaneous Lupus Erythematosus	53	0.047

191		GTR002	Goiter	53	0.047

192		HMC014	Homocysteinemia	53	0.047

193	P	ACT008	Actinic Keratosis	53	0.047

194		IMP005	Impotence	52	0.047

195		KRT009	Keratosis	51	0.047

196		CCT002	Cicatricial Pemphigoid	51	0.047

197		HYP017	Hypophosphatemia	50	0.047

198		47X002	47,xyy	49	0.047

199		HLX001	Helix Syndrome	47	0.047

200	P	ATX024	Ataxia-Oculomotor Apraxia 3	44	0.047

201		DBT002	Diabetic Autonomic Neuropathy	41	0.047

202		ALL014	Allergic Encephalomyelitis	38	0.047

203		GLC105	Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency	35	0.047

204	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.047

205		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.047

206	c	LKM061	Leukemia, Acute Myeloid	84	0.041

207		OST012	Osteoarthritis	78	0.041

208	P	LNG064	Lung Cancer Susceptibility 3	78	0.041

209		AST005	Asthma	76	0.041

210	P	RSP003	Respiratory Failure	74	0.041

211		SCK003	Sickle Cell Anemia	74	0.041

212		SVR004	Severe Combined Immunodeficiency	73	0.041

213	P	MLT020	Multiple Sclerosis	72	0.041

214		PRP027	Peripheral Vascular Disease	71	0.041

215		DWN001	Down Syndrome	70	0.041

216	P	LPR021	Leprosy 3	69	0.041

217	P	HYP802	Hypocalcemia, Autosomal Dominant 1	69	0.041

218	P	TRN020	Turner Syndrome	67	0.041

219		FLL027	Fallopian Tube Carcinoma	67	0.041

220		OST159	Osteogenic Sarcoma	66	0.041

221	P	MCR115	Microvascular Complications of Diabetes 5	66	0.041

222	P	PLM036	Pulmonary Fibrosis	65	0.041

223		SRC014	Sarcoma	65	0.041

224	c	JVN010	Juvenile Rheumatoid Arthritis	64	0.041

225	P	PRD008	Periodontitis	64	0.041

226		KRN002	Kearns-Sayre Syndrome	63	0.041

227		LSH001	Leishmaniasis	63	0.041

228		CLT003	Colitis	62	0.041

229	P	PLY014	Polycystic Kidney Disease	62	0.041

230		LVR012	Liver Cirrhosis	62	0.041

231		NPH091	Nephrolithiasis, Calcium Oxalate	60	0.041

232	P	KDN017	Kidney Cancer	60	0.041

233	c	JVN061	Juvenile Arthritis	60	0.041

234		LNG099	Lung Disease	60	0.041

235	P	CTR002	Cataract	60	0.041

236	P	BRS044	Breast Adenocarcinoma	59	0.041

237	c	CHL140	Chilblain Lupus 1	58	0.041

238		PMP006	Pemphigus Vulgaris, Familial	57	0.041

239	P	BPL003	Bipolar Disorder	56	0.041

240	c	BSL024	Basal Cell Carcinoma 1	56	0.041

241	P	PLY011	Polycystic Ovary Syndrome	56	0.041

242	c	ACT134	Acute Liver Failure	56	0.041

243		BCT022	Bacterial Infectious Disease	56	0.041

244		MCS002	Mucositis	56	0.041

245		BRN004	Brain Edema	56	0.041

246	P	PLY019	Polyneuropathy	56	0.041

247	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.041

248	P	MLN007	Male Infertility	55	0.041

249		NPH009	Nephrolithiasis	55	0.041

250	P	ART021	Arteriosclerosis	54	0.041

251	P	LTR001	Lateral Sclerosis	54	0.041

252		CLR030	Clear Cell Renal Cell Carcinoma	53	0.041

253	P	INS002	in Situ Carcinoma	53	0.041

254	P	RTN016	Retinal Degeneration	53	0.041

255		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	53	0.041

256		SPN035	Spindle Cell Sarcoma	53	0.041

257		PRP080	Peripheral Artery Disease	53	0.041

258		LNG031	Lung Benign Neoplasm	51	0.041

259	c	SCN007	Secondary Hyperparathyroidism	51	0.041

260		SKN013	Skin Benign Neoplasm	51	0.041

261		HYP781	Hypoascorbemia	51	0.041

262		HYP081	Hypolipoproteinemia	51	0.041

263	P	OVR082	Overgrowth Syndrome	50	0.041

264		HRT031	Hartnup Disorder	50	0.041

265		SYS003	Systolic Heart Failure	49	0.041

266	P	OPN001	Open-Angle Glaucoma	49	0.041

267		HYP043	Hyperandrogenism	48	0.041

268	c	HRD026	Hereditary Ataxia	48	0.041

269		ATS010	Autosomal Recessive Disease	48	0.041

270		SPL018	Splenomegaly	48	0.041

271		PRD004	Prediabetes Syndrome	47	0.041

272		RNL077	Renal Fibrosis	47	0.041

273	c	CHR095	Chronic Progressive External Ophthalmoplegia	46	0.041

274	c	PCH010	Pachyonychia Congenita 3	44	0.041

275	P	MTC004	Mitochondrial Encephalomyopathy	44	0.041

276	c	HYP272	Hypercholesterolemia, Familial, 3	44	0.041

277		CVD001	Covid-19	44	0.041

278		TRP009	Triple X Syndrome	42	0.041

279	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.041

280	P	KLZ004	Kala-Azar 1	41	0.041

281		RST023	Resting Heart Rate, Variation in	41	0.041

282	c	MJR024	Major Affective Disorder 9	41	0.041

283	P	HRD086	Hereditary Hypophosphatemic Rickets	40	0.041

284		SPR126	Superior Semicircular Canal Dehiscence	40	0.041

285	c	HMG029	Hemoglobin Se Disease	39	0.041

286	c	OVR114	Ovarian Cancer 1	38	0.041

287	c	SYS043	Systemic Lupus Erythematosus 1	38	0.041

288	c	MJR022	Major Affective Disorder 8	38	0.041

289		HNS001	Hansen's Disease	34	0.041

290		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.041

291		TMR016	Tumor Suppressor Gene on Chromosome 11	28	0.041

292		MYL069	Myeloma, Multiple	85	0.033

293		NRL016	Neural Tube Defects	82	0.033

294	P	ATX030	Ataxia-Telangiectasia	82	0.033

295		IMM167	Immune Deficiency Disease	78	0.033

296	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.033

297	P	CNR004	Cone-Rod Dystrophy 2	73	0.033

298		ANX010	Anxiety	73	0.033

299	P	LFR001	Li-Fraumeni Syndrome	72	0.033

300		HMN044	Human Immunodeficiency Virus Type 1	71	0.033

301	P	EPL164	Epilepsy	71	0.033

302	P	ATS364	Autism	70	0.033

303		MYL005	Myelofibrosis	70	0.033

304		PLM001	Pulmonary Tuberculosis	69	0.033

305	P	ART022	Arthritis	69	0.033

306		LYM133	Lymphoma, Hodgkin, Classic	69	0.033

307	P	HYP086	Hypothyroidism	69	0.033

308	P	LKM002	Leukemia	68	0.033

309		BRN024	Bronchitis	68	0.033

310	c	ATS007	Autism Spectrum Disorder	67	0.033

311	c	MGR028	Migraine with or Without Aura 1	67	0.033

312	c	RHB024	Rhabdomyosarcoma 2	67	0.033

313		ANG054	Angina Pectoris	66	0.033

314	P	NSP012	Nasopharyngeal Carcinoma	66	0.033

315	c	MCR129	Microvascular Complications of Diabetes 1	66	0.033

316		CHG001	Chagas Disease	66	0.033

317	P	CCK001	Cockayne Syndrome	66	0.033

318	c	MCL013	Mucolipidosis Iv	66	0.033

319	P	MTR014	Motor Neuron Disease	65	0.033

320	P	RHB003	Rhabdomyosarcoma	63	0.033

321	P	GLM045	Glioma	63	0.033

322	P	ANR048	Aniridia 1	63	0.033

323	P	CRN300	Coronary Heart Disease 1	63	0.033

324	P	MVM001	Movement Disease	63	0.033

325	c	ACT068	Acute Cystitis	63	0.033

326		TRN015	Transient Cerebral Ischemia	63	0.033

327		DPR016	Depression	63	0.033

328	c	GLC092	Glaucoma, Primary Open Angle	62	0.033

329	P	HYP750	Hypertriglyceridemia, Familial	62	0.033

330		LSC001	Lesch-Nyhan Syndrome	62	0.033

331		CRC021	Carcinosarcoma	62	0.033

332		BLD131	Bladder Urothelial Carcinoma	62	0.033

333		ACQ007	Acquired Immunodeficiency Syndrome	60	0.033

334		MTC146	Mitochondrial Complex I Deficiency, Nuclear Type 1	60	0.033

335	P	OPT006	Optic Nerve Disease	60	0.033

336	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.033

337	P	BND020	Bone Disease	59	0.033

338	c	HPT016	Hepatitis B	59	0.033

339	P	SLP005	Sleep Disorder	59	0.033

340	P	CYS018	Cystitis	59	0.033

341		FBR047	Fibromyalgia	58	0.033

342	P	URT039	Urticaria	58	0.033

343		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.033

344		GLS018	Glass Syndrome	57	0.033

345		BRN056	Bronchopulmonary Dysplasia	57	0.033

346	P	RHN004	Rhinitis	57	0.033

347		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.033

348	c	FML035	Familial Hyperlipidemia	55	0.033

349		HYP005	Hypokalemia	55	0.033

350	P	SCK002	Sick Sinus Syndrome	55	0.033

351		MCL006	Macular Retinal Edema	55	0.033

352	P	DRM007	Dermatitis Herpetiformis	55	0.033

353		AMN003	Amnestic Disorder	54	0.033

354		PRT038	Protein-Energy Malnutrition	54	0.033

355		PLM010	Pulmonary Edema	54	0.033

356		AMN001	Amenorrhea	54	0.033

357	P	LCH002	Lichen Planus	53	0.033

358		GLC042	Glucocorticoid Deficiency 1	53	0.033

359		GST023	Gastric Ulcer	53	0.033

360	c	GLL024	Gallbladder Disease 1	53	0.033

361		PRP016	Paraplegia	52	0.033

362		ACR041	Acromelic Frontonasal Dysostosis	52	0.033

363		NRT004	Neuritis	52	0.033

364		DYS015	Dysentery	52	0.033

365		TLN003	Telangiectasis	52	0.033

366		LMY002	Leiomyoma	52	0.033

367	c	SCN036	Secondary Progressive Multiple Sclerosis	51	0.033

368	c	PRM108	Primary Progressive Multiple Sclerosis	51	0.033

369		ADR042	Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency	50	0.033

370		RTN003	Retinal Ischemia	50	0.033

371		VTR016	Vater/vacterl Association	50	0.033

372		PLC008	Placenta Disease	50	0.033

373	P	OBS001	Obstructive Jaundice	50	0.033

374		DBT004	Diabetic Polyneuropathy	49	0.033

375		ENT004	Enthesopathy	49	0.033

376	P	END046	Endometritis	49	0.033

377		CHL004	Cholelithiasis	49	0.033

378	P	CTN015	Cutaneous T Cell Lymphoma	49	0.033

379		BLD044	Bladder Disease	48	0.033

380		DGN001	Degenerative Disc Disease	48	0.033

381		SXL003	Sexual Disorder	47	0.033

382		KRT002	Keratomalacia	47	0.033

383		CHR074	Choriocarcinoma	47	0.033

384	P	OVR046	Ovarian Cyst	47	0.033

385	P	MTH007	Methemoglobinemia	46	0.033

386		GLL048	Glial Tumor	45	0.033

387	c	LFR007	Li-Fraumeni Syndrome 2	45	0.033

388		ATN004	Autonomic Neuropathy	45	0.033

389		GRD001	Giardiasis	45	0.033

390		MYF001	Myofibroma	45	0.033

391		LRY018	Laryngeal Squamous Cell Carcinoma	44	0.033

392		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	43	0.033

393	P	HYP265	Hypotonia	43	0.033

394		PMP004	Pemphigus Foliaceus	43	0.033

395		VCT001	Vacterl Association	42	0.033

396		URM005	Uremic Pruritus	42	0.033

397		LRY017	Laryngeal Disease	42	0.033

398		ACT088	Acute Insulin Response	41	0.033

399		PMP002	Pemphigoid Gestationis	39	0.033

400	c	PLY105	Polycystic Ovary Syndrome 1	38	0.033

401		VCT005	Vacterl Association, X-Linked, with or Without Hydrocephalus	38	0.033

402		HRN029	Hearing Loss, Noise-Induced	37	0.033

403	c	DRM040	Dermatitis Herpetiformis, Familial	35	0.033

404		CND006	Candida Glabrata	32	0.033

405		PLR005	Pleuropneumonia	31	0.033

406		PMP008	Pemphigus Vegetans	27	0.033

407		STN013	Stenotrophomonas Maltophilia Infection	25	0.033

408		MTC015	Mitochondrial Dna-Associated Leigh Syndrome and Narp	24	0.033

409		PMP013	Pemphigus Gestationis	19	0.033

410	c	CHR688	Chronic Acquired Demyelinating Polyneuropathy	19	0.033

411	c	PLL014	Pellagra-Like Syndrome	18	0.033

412		MLR004	Malaria	81	0.024

413		CYS001	Cystic Fibrosis	81	0.024

414		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.024

415	P	RTN008	Retinitis Pigmentosa	79	0.024

416		GST019	Gastrointestinal Stromal Tumor	78	0.024

417	c	TBR025	Tuberous Sclerosis 1	77	0.024

418		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.024

419		PHN003	Phenylketonuria	75	0.024

420	c	ART115	Aortic Valve Disease 1	75	0.024

421		END057	Endometrial Cancer	74	0.024

422		LPT014	Leptin Deficiency or Dysfunction	74	0.024

423	P	OST002	Osteoporosis	74	0.024

424		XRD010	Xeroderma Pigmentosum, Variant Type	73	0.024

425		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.024

426	P	GRF003	Graft-Versus-Host Disease	72	0.024

427	P	PHC003	Pheochromocytoma	71	0.024

428		ACR007	Acromegaly	71	0.024

429	P	SRC025	Sarcoidosis 1	70	0.024

430		LGH007	Leigh Syndrome	70	0.024

431	c	EPL184	Epileptic Encephalopathy, Early Infantile, 6	70	0.024

432		ADN011	Adenoid Cystic Carcinoma	70	0.024

433	P	TTR001	Tetralogy of Fallot	70	0.024

434		ADL002	Adult Syndrome	70	0.024

435	P	TBR001	Tuberous Sclerosis	70	0.024

436	P	ASP006	Aspergillosis	69	0.024

437		PLY001	Polycythemia Vera	69	0.024

438		CRB037	Cerebral Palsy	69	0.024

439		EWN003	Ewing Sarcoma	69	0.024

440	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.024

441		MNT001	Mantle Cell Lymphoma	69	0.024

442	c	MYT021	Myotonic Dystrophy 1	69	0.024

443	P	SPR120	Supranuclear Palsy, Progressive, 1	68	0.024

444	P	PNM007	Pneumonia	68	0.024

445		OBS002	Obsessive-Compulsive Disorder	68	0.024

446	P	ESS003	Essential Thrombocythemia	68	0.024

447	P	MJR001	Major Depressive Disorder	68	0.024

448		PNC129	Pancreatic Adenocarcinoma	68	0.024

449	P	HPT021	Hepatitis	67	0.024

450	c	PRD013	Periodic Fever, Familial, Autosomal Dominant	67	0.024

451	c	INF071	Inflammatory Bowel Disease 1	67	0.024

452	P	FLL037	Follicular Lymphoma	67	0.024

453		ALL003	Allergic Rhinitis	67	0.024

454		PSY004	Psychotic Disorder	67	0.024

455	P	HYP098	Hypereosinophilic Syndrome	67	0.024

456	c	PLY168	Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease	66	0.024

457		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.024

458	c	FML021	Familial Hypercholesterolemia	66	0.024

459	P	MSC005	Muscular Dystrophy	66	0.024

460		ADR054	Adrenocortical Carcinoma, Hereditary	66	0.024

461	P	ATR011	Atrial Fibrillation	66	0.024

462	P	MNN013	Meningitis	66	0.024

463		MYL031	Myeloproliferative Neoplasm	66	0.024

464	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.024

465	P	DYS154	Dystonia	65	0.024

466		PPL049	Papillon-Lefevre Syndrome	65	0.024

467		TNG002	Tangier Disease	65	0.024

468		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.024

469		PND002	Pendred Syndrome	65	0.024

470	c	ART101	Aortic Valve Disease 2	65	0.024

471		IRR002	Irritable Bowel Syndrome	65	0.024

472		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	0.024

473	P	PRS038	Personality Disorder	65	0.024

474		CRN296	Carnitine Palmitoyltransferase Ii Deficiency, Infantile	65	0.024

475	P	CHR071	Charcot-Marie-Tooth Disease	65	0.024

476	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	65	0.024

477		APN008	Apnea, Obstructive Sleep	64	0.024

478		GT001	Gout	64	0.024

479		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.024

480		BRC012	Brucellosis	64	0.024

481		ART002	Arts Syndrome	64	0.024

482	P	FTL069	Fetal Akinesia Deformation Sequence 1	64	0.024

483		OST017	Osteomyelitis	64	0.024

484	P	HML002	Hemolytic Anemia	63	0.024

485	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.024

486	P	THR117	Three M Syndrome 1	63	0.024

487		CHN016	Cohen Syndrome	63	0.024

488	P	LMY004	Leiomyosarcoma	63	0.024

489	c	OPT053	Optic Atrophy 1	63	0.024

490	c	ALP101	Alpha-Thalassemia	62	0.024

491	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.024

492		HMT002	Hematologic Cancer	62	0.024

493		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	0.024

494	c	HPT001	Hepatitis C	62	0.024

495	c	HPT003	Hepatitis a	62	0.024

496		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.024

497		HYD038	Hydrops Fetalis, Nonimmune	62	0.024

498	P	VSC011	Vasculitis	62	0.024

499		PHL006	Phelan-Mcdermid Syndrome	62	0.024

500		MDD011	Mood Disorder	62	0.024

501		MSL001	Measles	62	0.024

502	P	DRM010	Dermatomyositis	61	0.024

503	c	CRB172	Cerebral Amyloid Angiopathy, Cst3-Related	61	0.024

504		OST003	Osteonecrosis	61	0.024

505		INT002	Intermittent Claudication	61	0.024

506	c	PNS012	Paine Syndrome	61	0.024

507		ALC006	Alcoholic Hepatitis	61	0.024

508		WLD007	Waldenstroem's Macroglobulinemia	61	0.024

509	P	PNC044	Pancreatitis	61	0.024

510	P	ART067	Aortic Aneurysm, Familial Thoracic 1	61	0.024

511		DRR016	Diarrhea 2, with Microvillus Atrophy	60	0.024

512	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.024

513		STT001	Status Epilepticus	60	0.024

514	P	THL005	Thalassemia	60	0.024

515	P	MCR010	Microcephaly	59	0.024

516		IDP011	Idiopathic Interstitial Pneumonia	59	0.024

517		CHL123	Chlamydia	59	0.024

518	P	MLN069	Melanoma, Uveal	59	0.024

519	c	HYD046	Hydatidiform Mole, Recurrent, 1	59	0.024

520		IRN001	Iron Deficiency Anemia	59	0.024

521		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.024

522	P	PLY006	Polydactyly	59	0.024

523		PPT005	Peptic Ulcer Disease	59	0.024

524		INC002	Inclusion Body Myositis	58	0.024

525	P	PLY017	Polyarteritis Nodosa	58	0.024

526	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.024

527		ANT024	Anthrax Disease	58	0.024

528		PST028	Post-Traumatic Stress Disorder	58	0.024

529	P	HYP726	Hypercalcemia, Infantile, 1	58	0.024

530	c	BNG091	Benign Chronic Pemphigus	58	0.024

531	P	ALC033	Alcohol Use Disorder	58	0.024

532		CNT047	Contact Dermatitis	58	0.024

533		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.024

534		EYD002	Eye Disease	58	0.024

535		DSS008	Disease of Mental Health	58	0.024

536		CRV038	Cervical Squamous Cell Carcinoma	58	0.024

537		MNT002	Mental Depression	58	0.024

538		CHL028	Childhood Type Dermatomyositis	58	0.024

539		APP015	Apparent Mineralocorticoid Excess	58	0.024

540		LYM027	Lymphopenia	58	0.024

541	P	CND004	Candidiasis	58	0.024

542	P	GLM007	Glomerulonephritis	57	0.024

543		GRN051	Granulomatous Disease, Chronic, X-Linked	57	0.024

544		IRN002	Iron Metabolism Disease	57	0.024

545		MNR012	Meniere Disease	57	0.024

546		DSS009	Disseminated Intravascular Coagulation	57	0.024

547		THY122	Thyroid Gland Cancer	57	0.024

548		THR024	Thrombosis	57	0.024

549	c	MYT020	Myotonic Dystrophy 2	57	0.024

550		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.024

551	P	FTL001	Fetal Alcohol Syndrome	57	0.024

552		CHR177	Chromophobe Renal Cell Carcinoma	57	0.024

553		BLR008	Bilirubin Metabolic Disorder	57	0.024

554		VSC002	Vascular Dementia	57	0.024

555	P	LKD017	Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism	57	0.024

556	P	PYL005	Pyelonephritis	56	0.024

557	P	MYS005	Myositis	56	0.024

558	P	PLY018	Polycythemia	56	0.024

559	c	MSC109	Mosaic Variegated Aneuploidy Syndrome 1	56	0.024

560		CMR002	Coumarin Resistance	56	0.024

561		LST001	Listeriosis	56	0.024

562		TRN018	Transitional Cell Carcinoma	56	0.024

563		LBL001	Lobular Neoplasia	56	0.024

564		LMY014	Leiomyoma, Uterine	56	0.024

565		ERY051	Erythroleukemia, Familial	56	0.024

566		SFT003	Soft Tissue Sarcoma	56	0.024

567		SCH003	Schizophreniform Disorder	56	0.024

568		HMG005	Hemoglobinopathy	56	0.024

569	P	NRF002	Neurofibromatosis	56	0.024

570		GST050	Gastrointestinal System Disease	56	0.024

571	P	HYP838	Hyperlipidemia, Familial Combined, 3	56	0.024

572	P	GST044	Gastritis	56	0.024

573	c	CHR627	Charcot-Marie-Tooth Disease, Demyelinating, Type 1a	55	0.024

574		ATR057	Atrioventricular Block	55	0.024

575		NRN004	Neuroendocrine Tumor	55	0.024

576	c	CRD184	Ceroid Lipofuscinosis, Neuronal, 5	55	0.024

577		ORL004	Oral Submucous Fibrosis	55	0.024

578		LMB062	Limb Ischemia	55	0.024

579		DFF005	Diffuse Large B-Cell Lymphoma	55	0.024

580		ISL014	Isolated Growth Hormone Deficiency, Type Ia	55	0.024

581		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.024

582		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.024

583	P	SBS003	Substance Abuse	55	0.024

584		HDR002	Hidradenitis Suppurativa	55	0.024

585		BRN045	Brunner Syndrome	55	0.024

586	c	ATM024	Autoimmune Pancreatitis	55	0.024

587		HMZ003	Homozygous Familial Hypercholesterolemia	55	0.024

588		END040	Endogenous Depression	55	0.024

589		INT007	Intermediate Coronary Syndrome	55	0.024

590	P	SLM003	Salmonellosis	55	0.024

591		ACD008	Acid-Labile Subunit Deficiency	54	0.024

592		SJG002	Sjogren-Larsson Syndrome	54	0.024

593		PRT082	Preterm Premature Rupture of the Membranes	54	0.024

594	P	CNT116	Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a	54	0.024

595	P	CYS039	Cystic Kidney Disease	54	0.024

596		AMY027	Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1	54	0.024

597		HMS001	Hemosiderosis	54	0.024

598		LYM040	Lymphoblastic Lymphoma	54	0.024

599		SLP001	Sleeping Sickness	54	0.024

600	c	SPN294	Spinocerebellar Ataxia 1	53	0.024

601	c	CNT016	Central Retinal Vein Occlusion	53	0.024

602		HRT012	Heart Valve Disease	53	0.024

603	P	MNC007	Monocytic Leukemia	53	0.024

604		PRP036	Peripheral T-Cell Lymphoma	53	0.024

605		OCL006	Ocular Hypertension	53	0.024

606		MST005	Mastitis	53	0.024

607	c	PRM092	Primary Lateral Sclerosis, Adult, 1	53	0.024

608		CLF001	Cleft Lip	53	0.024

609	c	HRM017	Hermansky-Pudlak Syndrome 2	53	0.024

610		NNT012	Neonatal Jaundice	53	0.024

611		NRT001	Neurotic Disorder	53	0.024

612		TXC002	Toxic Encephalopathy	53	0.024

613		PRN011	Pernicious Anemia	53	0.024

614	P	RTN022	Retinal Vein Occlusion	53	0.024

615	c	HYP740	Hyperlipoproteinemia, Type V	53	0.024

616	c	HPT007	Hepatitis E	53	0.024

617		TRC008	Trachoma	53	0.024

618		EXP004	Exophthalmos	52	0.024

619		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.024

620		DRM011	Dermatophytosis	52	0.024

621	c	VRL010	Viral Hepatitis	52	0.024

622	c	SPN291	Spinocerebellar Ataxia 7	52	0.024

623		CRT016	Carotid Artery Disease	52	0.024

624		THY030	Thyroid Gland Disease	52	0.024

625	P	MSC003	Muscular Atrophy	52	0.024

626		NRP045	Neuropathy, Ataxia, and Retinitis Pigmentosa	52	0.024

627		BWN001	Bowen-Conradi Syndrome	52	0.024

628		LGN006	Legionnaire Disease	52	0.024

629		HYP014	Hyperuricemia	52	0.024

630	c	ACT135	Acute Graft Versus Host Disease	52	0.024

631	c	HYP843	Hypoalphalipoproteinemia, Primary, 2	52	0.024

632		SPS003	Spastic Diplegia	51	0.024

633	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.024

634		OCL069	Ocular Motor Apraxia	51	0.024

635		AVD001	Avoidant Personality Disorder	51	0.024

636		FDL002	Food Allergy	51	0.024

637		PLS009	Plasma Cell Neoplasm	51	0.024

638		THR016	Thrombophlebitis	51	0.024

639		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.024

640		SCH012	Schizoaffective Disorder	50	0.024

641		PLR008	Pleurisy	50	0.024

642		PRS034	Parasitic Helminthiasis Infectious Disease	50	0.024

643		PST021	Postpartum Depression	50	0.024

644		CRT013	Carotid Stenosis	50	0.024

645		MCL027	Macular Dystrophy, Dominant Cystoid	50	0.024

646		TRY001	Trypanosomiasis	50	0.024

647		NTR046	Neutrophil Migration	50	0.024

648		MTB004	Metabolic Acidosis	50	0.024

649		OPT003	Opiate Dependence	50	0.024

650		LPR001	Lepromatous Leprosy	50	0.024

651		HYP080	Hypogonadism	50	0.024

652		RNL011	Renal Osteodystrophy	50	0.024

653		ONC007	Oncocytoma	49	0.024

654		PLP001	Pulpitis	49	0.024

655		HDR003	Hidradenitis	49	0.024

656		SLD003	Sialadenitis	49	0.024

657		MCR004	Macroglobulinemia	49	0.024

658		DYS009	Dysthymic Disorder	49	0.024

659		IMP004	Impetigo	49	0.024

660		ACT029	Acute Interstitial Pneumonia	49	0.024

661		PTH002	Pathological Gambling	49	0.024

662		URM002	Uremia	49	0.024

663		VCC001	Vaccinia	49	0.024

664		ADR016	Adrenal Cortical Carcinoma	48	0.024

665	c	ACT150	Acute Adrenal Insufficiency	48	0.024

666		NRL018	Neural Tube Defects, Folate-Sensitive	48	0.024

667		SBS004	Substance Dependence	48	0.024

668		CLC006	Calcinosis	48	0.024

669		VTM033	Vitamin K Deficiency Bleeding	48	0.024

670	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.024

671		DBT006	Diabetic Macular Edema	48	0.024

672		RCT020	Rectum Adenocarcinoma	48	0.024

673	P	KRT005	Keratoacanthoma	48	0.024

674		ART004	Aortic Atherosclerosis	47	0.024

675		PHS004	Phosphoribosylpyrophosphate Synthetase Superactivity	47	0.024

676		CRY008	Cryopyrin-Associated Periodic Syndrome	47	0.024

677		ABD017	Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2	47	0.024

678	P	RNL015	Renal Hypertension	47	0.024

679		ACT084	Acute Stress Disorder	47	0.024

680		ANT011	Antisocial Personality Disorder	47	0.024

681		KHN001	Kuhnt-Junius Degeneration	47	0.024

682		LYM012	Lymphoplasmacytic Lymphoma	47	0.024

683		TTR011	Tetraploidy	47	0.024

684		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.024

685		HYP082	Hypopharynx Cancer	47	0.024

686		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.024

687	c	PRM093	Premature Ovarian Failure 7	47	0.024

688		LYM019	Lymphosarcoma	46	0.024

689	P	PRC019	Precocious Puberty	46	0.024

690		RTN023	Retinitis	46	0.024

691	P	VTR007	Vitreoretinopathy	46	0.024

692		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.024

693		LPD009	Lipid Storage Disease	46	0.024

694		RTN020	Retinal Vascular Disease	46	0.024

695	c	CRV002	Cervix Uteri Carcinoma in Situ	46	0.024

696		TTH006	Tooth Disease	46	0.024

697	c	GRN049	Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I	46	0.024

698		KRT013	Keratolytic Winter Erythema	46	0.024

699		OBS003	Obsessive-Compulsive Personality Disorder	46	0.024

700	c	SCH079	Schizophrenia 1	46	0.024

701		GRW007	Growth Hormone Deficiency	46	0.024

702		GST010	Gestational Trophoblastic Neoplasm	46	0.024

703		OPD001	Opioid Abuse	46	0.024

704	c	DRR009	Diarrhea 6	46	0.024

705	P	HYP733	Hypercalciuria, Absorptive, 2	45	0.024

706		URT010	Ureteral Obstruction	45	0.024

707		TRT001	Teratocarcinoma	45	0.024

708		CYN002	Cyanosis, Transient Neonatal	45	0.024

709		DST006	Diastolic Heart Failure	45	0.024

710		GLC098	Glaucoma-Related Pigment Dispersion Syndrome	45	0.024

711		CLC017	Calcification of Joints and Arteries	45	0.024

712		MLN073	Melanosis, Neurocutaneous	45	0.024

713	P	SBR004	Seborrheic Dermatitis	45	0.024

714		CNT017	Central Nervous System Origin Vertigo	45	0.024

715		SPS057	Spasticity	45	0.024

716		ASP026	Asplenia, Isolated Congenital	44	0.024

717		RTR001	Retrograde Amnesia	44	0.024

718	c	DRM054	Dermatitis, Atopic, 2	44	0.024

719		CNN002	Cannabis Abuse	44	0.024

720		DWR001	Dwarfism	44	0.024

721		CRB008	Cerebral Atherosclerosis	44	0.024

722		OVR063	Overnutrition	44	0.024

723		FML091	Familial Tumoral Calcinosis	44	0.024

724		SYR002	Syringocystadenoma Papilliferum	44	0.024

725	P	BNG095	Benign Giant Cell Tumor	44	0.024

726	c	PRM038	Primary Agammaglobulinemia	44	0.024

727	P	HYP121	Hypoalphalipoproteinemia	43	0.024

728		GLC086	Glucocorticoid-Induced Osteoporosis	43	0.024

729		SBC012	Subcorneal Pustular Dermatosis	43	0.024

730	c	FTL006	Fetal Alcohol Spectrum Disorder	43	0.024

731	P	MJR007	Major Affective Disorder 1	43	0.024

732		PHY002	Physical Disorder	42	0.024

733		HDG002	Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance	42	0.024

734		ALC010	Alcoholic Cardiomyopathy	42	0.024

735	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.024

736	c	GRN050	Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type Ii	42	0.024

737	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.024

738		MNN017	Mononeuropathy	42	0.024

739		BCK006	Back Pain	42	0.024

740		ATX019	Ataxia with Vitamin E Deficiency	42	0.024

741		CTS005	Catastrophic Antiphospholipid Syndrome	42	0.024

742		OBS082	Obstructive Nephropathy	42	0.024

743		MYF002	Myofascial Pain Syndrome	42	0.024

744		NRR001	Neuroretinitis	42	0.024

745		PSD001	Pseudobulbar Palsy	42	0.024

746	c	HYP841	Hypoalphalipoproteinemia, Primary, 1	41	0.024

747		CRB025	Carbohydrate Metabolic Disorder	41	0.024

748		MMM006	Mammographic Density	41	0.024

749		PRS063	Paresthesia	41	0.024

750	P	RRH023	Rare Hereditary Hemochromatosis	41	0.024

751		KLB003	Klebsiella Pneumonia	41	0.024

752	c	MCR112	Microvascular Complications of Diabetes 2	41	0.024

753		VSL013	Visual Impairment and Progressive Phthisis Bulbi	41	0.024

754		RDN001	Reading Disorder	40	0.024

755	P	MLG074	Malignant Mesenchymoma	40	0.024

756		LNR006	Linear Iga Disease	40	0.024

757		CLD014	Cole Disease	40	0.024

758		GLC008	Glucose Metabolism Disease	40	0.024

759	P	PRG092	Pregnancy Loss, Recurrent 1	40	0.024

760		SCH011	Schizotypal Personality Disorder	40	0.024

761		PLY100	Polyploidy	40	0.024

762		CNN001	Cannabis Dependence	40	0.024

763		CHL045	Choline Deficiency Disease	39	0.024

764		LNG030	Lung Adenoma	39	0.024

765		CRV045	Cervical Intraepithelial Neoplasia	39	0.024

766		ADR004	Adrenal Cortical Adenocarcinoma	39	0.024

767		BLL012	Bullous Impetigo	39	0.024

768		HYP344	Hyperthyroidism, Familial Gestational	39	0.024

769	c	HYP555	Hypertriglyceridemia, Transient Infantile	39	0.024

770		AML001	Amelanotic Melanoma	39	0.024

771	c	CHR682	Chronic Bilirubin Encephalopathy	39	0.024

772		NCR002	Necrobiosis Lipoidica	38	0.024

773		OVR094	Ovarian Epithelial Cancer	38	0.024

774		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.024

775	c	SCH051	Schizophrenia 4	37	0.024

776		DBT081	Diabetic Encephalopathy	37	0.024

777	c	LPR022	Leprosy 2	37	0.024

778	c	CHR020	Chronic Interstitial Cystitis	37	0.024

779	c	CNG223	Congenital Methemoglobinemia	36	0.024

780		HRW001	Hair Whorl	36	0.024

781		ALC001	Alcohol-Related Birth Defect	36	0.024

782		MTH026	Methemoglobinemia Due to Deficiency of Methemoglobin Reductase	36	0.024

783		HYP114	Hypertensive Nephropathy	36	0.024

784		FST010	Fasting Hypoglycemia	35	0.024

785		NRD001	Neurodermatitis	35	0.024

786		PRG080	Progressive Non-Infectious Anterior Vertebral Fusion	35	0.024

787	c	MJR008	Major Affective Disorder 2	35	0.024

788		MYT011	Myotonia	34	0.024

789		PYR009	Pyridoxine Deficiency Anemia	34	0.024

790		24D001	2,4-Dienoyl-Coa Reductase Deficiency	34	0.024

791		LCH013	Lichen Planus Pemphigoides	34	0.024

792	c	MJR023	Major Affective Disorder 7	33	0.024

793		PPL052	Papillomatosis, Confluent and Reticulated	33	0.024

794	c	CHR064	Chronic Monocytic Leukemia	33	0.024

795	c	SCH083	Schizophrenia 7	33	0.024

796	c	MJR003	Major Affective Disorder 6	33	0.024

797	c	MJR006	Major Affective Disorder 5	33	0.024

798	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.024

799	c	SCH085	Schizophrenia 2	33	0.024

800	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.024

801		KDN013	Kidney Hypertrophy	32	0.024

802		NTR011	Neutrophil-Specific Granule Deficiency	32	0.024

803		ANN011	Annular Erythema	32	0.024

804	c	SCH080	Schizophrenia 3	32	0.024

805		PRX097	Paroxysmal Dystonia	32	0.024

806		SPC026	Specific Granule Deficiency 1	31	0.024

807	c	SCH082	Schizophrenia 5	31	0.024

808		CLS047	Classic Progressive Supranuclear Palsy Syndrome	31	0.024

809		ADR001	Adrenal Rest Tumor	30	0.024

810		CNJ001	Conjugate Gaze Palsy	29	0.024

811		CRD220	Cardiac Valvular Defect, Developmental	29	0.024

812	c	HYP839	Hyperlipidemia, Familial Combined, 1	29	0.024

813	c	MJR004	Major Affective Disorder 4	28	0.024

814	c	SCH084	Schizophrenia 8	28	0.024

815	P	OVR096	Overlap Myositis	27	0.024

816		HYD030	Hydroxykynureninuria	27	0.024

817		ARG004	Argyria	27	0.024

818		DMN026	Dementia Pugilistica	27	0.024

819		MLR020	Malaria, Mild	27	0.024

820		CHL079	Children's Interstitial Lung Disease	26	0.024

821	c	RNG015	Ring Chromosome 2	26	0.024

822		ACT162	Acute Sensory Ataxic Neuropathy	26	0.024

823		MTH071	Methane Production	26	0.024

824		ADG002	Audiogenic Seizures	25	0.024

825		NNT021	Neonatal Meningitis	25	0.024

826		TXC004	Toxic Diffuse Goiter	24	0.024

827		INT074	Intracranial Arteriosclerosis	23	0.024

828		HDG004	Hodgkin's Granuloma	23	0.024

829		HDG006	Hodgkin's Paragranuloma	22	0.024

830	c	RNG019	Ring Chromosome 3	22	0.024

831		HML018	Homologous Wasting Disease	22	0.024

832		CMB039	Combined Pulmonary Fibrosis-Emphysema Syndrome	20	0.024

833	P	RRN010	Rare Neurodegenerative Disease	20	0.024

834		BLD065	Blue Diaper Syndrome	20	0.024

835		DFN191	Deafness, Congenital Heart Defects, and Posterior Embryotoxon	20	0.024

836	c	VRT015	Vertebral, Cardiac, Renal, and Limb Defects Syndrome 2	19	0.024

837		NR0002	Nr0b1-Related Adrenal Hypoplasia Congenita	15	0.024

838		RCR030	Recurrent Idiopathic Neuroretinitis	11	0.024