Search results for FAD

904 hits were found for FAD

#	Family	MCID	Name	MIFTS	Score
1	P	FTL069	Fetal Akinesia Deformation Sequence 1	63	30.543

2	c	ERL029	Early-Onset, Autosomal Dominant Alzheimer Disease	59	14.293

3		MLT118	Multiple Acyl-Coa Dehydrogenase Deficiency	64	11.661

4	c	FTL070	Fetal Akinesia Deformation Sequence 2	36	6.391

5	P	ALZ034	Alzheimer Disease	87	6.167

6	c	FTL071	Fetal Akinesia Deformation Sequence 3	29	3.943

7		RBF001	Riboflavin Deficiency	49	2.424

8		DRM006	Dermatitis	61	2.417

9	c	ALZ056	Alzheimer Disease 3	56	2.300

10		FRN006	Frontotemporal Dementia	68	2.139

11	P	CHR012	Chronic Granulomatous Disease	69	2.116

12		CNG506	Congenital Amyoplasia	27	2.058

13		PCK003	Pick Disease of Brain	70	2.007

14	P	ACN016	Acne Inversa, Familial, 3	28	1.957

15		HLX001	Helix Syndrome	47	1.893

16		ETN001	Eating Disorder	59	1.822

17	P	DRM053	Dermatitis, Atopic	65	1.743

18	P	MYP004	Myopathy	67	1.583

19		ACY011	Acyl-Coa Dehydrogenase Deficiency	31	1.583

20		ART140	Arteries, Anomalies of	52	1.565

21		LPP008	Lipoprotein Quantitative Trait Locus	65	1.565

22	P	LYM118	Lymphoma	66	1.501

23		TCL023	T-Cell Lymphoma, Subcutaneous Panniculitis-Like	50	1.501

24		LYM019	Lymphosarcoma	46	1.501

25		CLF027	Cleft Palate, Isolated	64	1.498

26	P	NRB001	Neuroblastoma	66	1.448

27	P	DST002	Distal Arthrogryposis	63	1.426

28	P	DMN002	Dementia	65	1.353

29		PLY012	Polyhydramnios	46	1.340

30		BCK006	Back Pain	43	1.328

31	c	CRB172	Cerebral Amyloid Angiopathy, Cst3-Related	64	1.321

32	P	AMY004	Amyloidosis	69	1.315

33	P	MYC033	Myoclonus	46	1.315

34		AGN016	Aging	53	1.288

35		IRN002	Iron Metabolism Disease	56	1.288

36		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	1.279

37		MCL006	Macular Retinal Edema	56	1.260

38		DBT006	Diabetic Macular Edema	48	1.260

39		ATS010	Autosomal Recessive Disease	42	1.258

40		IRR002	Irritable Bowel Syndrome	64	1.221

41		MLD018	Mild Cognitive Impairment	48	1.217

42		RPD005	Rapidly Involuting Congenital Hemangioma	48	1.204

43		NNL005	Non-Alcoholic Fatty Liver Disease	63	1.204

44		PRT037	Pertussis	49	1.202

45	c	DLT002	Dilated Cardiomyopathy	79	1.168

46	P	MJR001	Major Depressive Disorder	68	1.162

47		LPD008	Lipid Metabolism Disorder	61	1.155

48		MNT002	Mental Depression	56	1.154

49		RST011	Restrictive Dermopathy, Lethal	51	1.145

50		CHG001	Chagas Disease	65	1.142

51	P	MYC008	Myocarditis	59	1.142

52	P	CNG001	Congenital Myasthenic Syndrome	68	1.128

53	P	CTR002	Cataract	59	1.128

54		SPS019	Spastic Paraparesis	38	1.120

55		FTT001	Fatty Liver Disease	61	1.114

56	P	ENC018	Encephalopathy	62	1.114

57		DWN001	Down Syndrome	70	1.113

58	P	SCL018	Scoliosis	57	1.099

59		PST011	Pustulosis of Palm and Sole	52	1.099

60	P	PSR002	Psoriasis	63	1.099

61	P	MTH007	Methemoglobinemia	46	1.093

62		SKN016	Skin Disease	63	1.083

63		DPR016	Depression	64	1.074

64	c	FTL072	Fetal Akinesia Deformation Sequence 4	37	1.068

65		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	1.067

66	c	ATR087	Atrial Standstill 1	74	1.067

67		CNG065	Congenital Contractures	27	1.067

68		APH002	Aphasia	55	1.055

69	P	AST005	Asthma	75	1.050

70		CND006	Candida Glabrata	29	1.050

71	c	MJR022	Major Affective Disorder 8	37	1.045

72	c	MJR024	Major Affective Disorder 9	40	1.045

73	P	PRK039	Parkinsonism	55	1.045

74	P	BPL003	Bipolar Disorder	56	1.045

75		ISC004	Ischemia	61	1.013

76	P	PRS040	Prostate Cancer	95	1.011

77	c	INH020	Inherited Metabolic Disorder	47	1.003

78		CHL014	Cholera	62	0.980

79	c	2HY001	2-Hydroxyglutaric Aciduria	38	0.968

80	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.968

81		CRN048	Craniofacial-Deafness-Hand Syndrome	52	0.956

82		HMC014	Homocysteinemia	52	0.956

83	c	CNG223	Congenital Methemoglobinemia	39	0.956

84	P	HNT016	Huntington Disease	73	0.956

85		HYP060	Hyperinsulinism	53	0.956

86		GLB002	Glioblastoma	67	0.956

87	P	SYP003	Syphilis	59	0.956

88		CNG538	Congenital Arthrogryposis with Anterior Horn Cell Disease	32	0.944

89	P	RCT021	Rectum Cancer	54	0.939

90		PPL052	Papillomatosis, Confluent and Reticulated	34	0.931

91	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	0.931

92	c	BDY006	Body Mass Index Quantitative Trait Locus 8	43	0.931

93	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.931

94	c	BDY020	Body Mass Index Quantitative Trait Locus 19	51	0.931

95	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.931

96	c	BDY012	Body Mass Index Quantitative Trait Locus 7	43	0.931

97	c	BDY019	Body Mass Index Quantitative Trait Locus 18	46	0.931

98	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.931

99	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.931

100	P	BDY004	Body Mass Index Quantitative Trait Locus 11	82	0.918

101	c	ATS307	Autosomal Recessive Cerebellar Ataxia	38	0.918

102		ARG004	Argyria	26	0.918

103	c	L2H001	L-2-Hydroxyglutaric Aciduria	49	0.904

104		LPD042	Lipid Storage Myopathy Due to Flavin Adenine Dinucleotide Synthetase Deficiency	22	0.904

105	P	MSC003	Muscular Atrophy	52	0.904

106		ALL014	Allergic Encephalomyelitis	34	0.904

107		MTB004	Metabolic Acidosis	48	0.890

108	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	0.890

109		MLR009	Miliaria	33	0.890

110		NRN004	Neuroendocrine Tumor	55	0.890

111	P	EPL164	Epilepsy	70	0.890

112		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.890

113		MLR001	Miliaria Rubra	32	0.890

114		CRC006	Carcinoid Syndrome	55	0.890

115		GRN051	Granulomatous Disease, Chronic, X-Linked	57	0.875

116	P	CLC063	Celiac Disease 1	65	0.865

117		CHR081	Choroideremia	58	0.865

118		CYN002	Cyanosis, Transient Neonatal	43	0.859

119		ANT003	Antley-Bixler Syndrome	50	0.859

120	P	HMC002	Homocystinuria	52	0.859

121		STN013	Stenotrophomonas Maltophilia Infection	26	0.859

122		ACY010	Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of	63	0.843

123		CYS002	Cystic Lymphangioma	45	0.843

124		PRT038	Protein-Energy Malnutrition	53	0.843

125		HYP056	Hypoglycemia	65	0.843

126	c	MCR115	Microvascular Complications of Diabetes 5	65	0.826

127	P	SPN046	Spinal Muscular Atrophy	62	0.826

128		BCT022	Bacterial Infectious Disease	55	0.826

129	c	ACT076	Acute Myocarditis	46	0.826

130		END086	End Stage Renal Disease	54	0.826

131		47X002	47,xyy	47	0.826

132		CRY035	Cryptorchidism, Unilateral or Bilateral	57	0.807

133	c	TYP009	Type 2 Diabetes Mellitus	91	0.807

134	P	TRM004	Trimethylaminuria	45	0.807

135		DNT012	Dental Caries	53	0.807

136		CHR178	Chromosomal Triplication	33	0.800

137		AMN003	Amnestic Disorder	53	0.788

138		STM007	Stomatitis	52	0.788

139	c	CRB175	Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1	70	0.766

140		HMC041	Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity	48	0.766

141		THM002	Thiamine-Responsive Megaloblastic Anemia Syndrome	50	0.766

142		ALP089	Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality	26	0.766

143		HYP748	Hypertelorism	46	0.766

144		CVT001	Cavitary Optic Disc Anomalies	38	0.766

145		GRD001	Giardiasis	46	0.766

146		CRV002	Cervix Uteri Carcinoma in Situ	48	0.766

147		CRV045	Cervical Intraepithelial Neoplasia	38	0.766

148		THY029	Thyroid Carcinoma	55	0.766

149		PRN039	Paraneoplastic Syndromes	37	0.765

150		PRT251	Proteinuria, Chronic Benign	58	0.742

151	P	CRN300	Coronary Heart Disease 1	73	0.742

152		HYD038	Hydrops Fetalis, Nonimmune	57	0.742

153	c	LYM150	Lymphatic Malformation 7	43	0.742

154	P	MYS003	Myasthenia Gravis	67	0.742

155		RSP021	Respiratory Allergy	41	0.742

156		PTH002	Pathological Gambling	48	0.742

157		NPH009	Nephrolithiasis	54	0.742

158		PRM209	Primary Trimethylaminuria	19	0.742

159	c	DRM054	Dermatitis, Atopic, 2	47	0.719

160		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.719

161		MCL027	Macular Dystrophy, Dominant Cystoid	51	0.719

162	P	MTR004	Maturity-Onset Diabetes of the Young	66	0.715

163	P	ATS364	Autism	72	0.715

164		LGH007	Leigh Syndrome	70	0.715

165		NPH091	Nephrolithiasis, Calcium Oxalate	61	0.715

166	P	CLR023	Colorectal Cancer	100	0.715

167		ANG054	Angina Pectoris	65	0.715

168	P	GST053	Gastric Cancer	82	0.715

169		PHN003	Phenylketonuria	76	0.715

170		MLT010	Multiple Personality Disorder	29	0.715

171		FDL002	Food Allergy	47	0.715

172		HYP014	Hyperuricemia	51	0.715

173		KWS001	Kwashiorkor	44	0.715

174		URN010	Urinary Tract Obstruction	55	0.715

175		LPT001	Leptospirosis	65	0.715

176	P	LVR013	Liver Disease	68	0.715

177	P	PRS038	Personality Disorder	65	0.715

178		MTC015	Mitochondrial Dna-Associated Leigh Syndrome and Narp	24	0.715

179		NCL011	Nuclear Gene-Encoded Leigh Syndrome Spectrum	21	0.715

180	c	ATS007	Autism Spectrum Disorder	71	0.683

181	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.683

182	c	MTR019	Maturity-Onset Diabetes of the Young, Type 2	53	0.683

183		ART002	Arts Syndrome	66	0.683

184		MYL069	Myeloma, Multiple	76	0.683

185	c	HYP595	Hypertension, Essential	84	0.683

186	c	MTR020	Maturity-Onset Diabetes of the Young, Type 3	54	0.683

187		CNT047	Contact Dermatitis	56	0.683

188	P	PLY011	Polycystic Ovary Syndrome	57	0.683

189	c	ALZ063	Alzheimer's Disease 1	32	0.653

190	c	ALZ054	Alzheimer Disease 4	44	0.645

191		MTC166	Mitochondrial Complex I Deficiency, Nuclear Type 19	23	0.641

192	c	SCN036	Secondary Progressive Multiple Sclerosis	55	0.641

193		PNG002	Pain Agnosia	51	0.641

194	P	INF037	Inflammatory Bowel Disease	53	0.641

195		OTT002	Otitis Media	70	0.641

196		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	0.641

197	P	EXN002	Exanthem	58	0.641

198	P	SPP010	Suppressor of Tumorigenicity 3	50	0.641

199		OBS082	Obstructive Nephropathy	41	0.641

200	P	FLL037	Follicular Lymphoma	66	0.641

201	P	ACN011	Acne	55	0.641

202		STT001	Status Epilepticus	58	0.641

203		MLK006	Milk Allergy	47	0.641

204		ALL010	Allergic Contact Dermatitis	55	0.641

205	P	MYT002	Myotonic Dystrophy	51	0.641

206		SKN019	Skin Melanoma	70	0.641

207	P	LPS004	Lupus Erythematosus	61	0.641

208	P	CHR345	Chronic Pain	50	0.641

209		NRL016	Neural Tube Defects	80	0.605

210		HYP266	Hypoxia	56	0.605

211		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	0.541

212	c	DRM040	Dermatitis Herpetiformis, Familial	35	0.541

213	P	RST001	Restless Legs Syndrome	52	0.541

214	P	CRP001	Carpal Tunnel Syndrome	65	0.541

215		PLY105	Polycystic Ovary Syndrome 1	39	0.541

216	c	PCH010	Pachyonychia Congenita 3	43	0.541

217		ATM095	Autoimmune Disease	61	0.541

218		TBS001	Tabes Dorsalis	30	0.541

219	P	VNS003	Venous Insufficiency	54	0.541

220		CHR001	Churg-Strauss Syndrome	61	0.541

221		WHT017	Wheat Allergy	30	0.541

222		FLL008	Folliculitis	45	0.541

223		CNS004	Constipation	56	0.541

224	P	ADL010	Adult Respiratory Distress Syndrome	70	0.541

225		PTL002	Patellofemoral Pain Syndrome	34	0.541

226	P	DRM007	Dermatitis Herpetiformis	54	0.541

227	P	SLP005	Sleep Disorder	61	0.541

228	P	CWD010	Cowden Syndrome	70	0.541

229	P	VSC011	Vasculitis	61	0.541

230		ANC002	Anca-Associated Vasculitis	44	0.541

231		PPT005	Peptic Ulcer Disease	58	0.541

232		APP008	Appendicitis	62	0.541

233		CHR066	Chronic Fatigue Syndrome	59	0.541

234	P	CLS010	Cluster Headache	42	0.541

235		MCR088	Microscopic Polyangiitis	51	0.541

236		ALL012	Allergic Angiitis	24	0.541

237		SPT023	Septate Uterus	31	0.541

238		ESN016	Eosinophilic Pustular Folliculitis	25	0.541

239		URM005	Uremic Pruritus	46	0.541

240		MLT163	Multiple Pterygium Syndrome, Escobar Variant	62	0.514

241	P	BRS053	Breast Fibroadenoma	48	0.504

242		NRM005	Neuromuscular Disease	62	0.494

243		ALL029	Allergic Disease	61	0.494

244		BRN071	Brain Injury	50	0.494

245		PRN009	Paranoid Schizophrenia	49	0.483

246		TRM010	Traumatic Brain Injury	50	0.483

247		APR001	Apraxia	51	0.473

248		MLT134	Multiple Pterygium Syndrome, Lethal Type	56	0.473

249		KRT009	Keratosis	52	0.473

250		ANR007	Anorexia Nervosa	59	0.462

251	P	HYP069	Hyperparathyroidism	62	0.462

252	c	ALZ049	Alzheimer Disease 2	48	0.439

253		ECT041	Ectodermal Dysplasia-Syndactyly Syndrome 2	35	0.439

254	c	AMY091	Amyotrophic Lateral Sclerosis 1	87	0.439

255	P	LTR001	Lateral Sclerosis	57	0.439

256		VRG001	Variegate Porphyria	55	0.428

257	P	PRP029	Porphyria	60	0.428

258		TCK004	Tick Infestation	29	0.428

259		PSY004	Psychotic Disorder	66	0.428

260	P	MYC084	Mycobacterium Tuberculosis 1	68	0.416

261		VSC002	Vascular Dementia	59	0.416

262		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	0.403

263	P	BRS047	Breast Cancer	97	0.403

264		PST028	Post-Traumatic Stress Disorder	58	0.403

265		MSC193	Muscular Lipidosis	23	0.403

266		INS024	Insulin-Like Growth Factor I	77	0.390

267	P	BRW001	Brown-Vialetto-Van Laere Syndrome	49	0.390

268		ADN018	Adenoma	58	0.390

269	P	AGN002	Agnosia	53	0.390

270	P	HYP265	Hypotonia	42	0.390

271		MNC011	Minicore Myopathy with External Ophthalmoplegia	38	0.377

272		CNT105	Central Core Disease of Muscle	59	0.377

273		FLL031	Follicular Adenoma	40	0.377

274		GTR002	Goiter	52	0.377

275	P	THL005	Thalassemia	56	0.377

276		HLT001	Holt-Oram Syndrome	66	0.363

277	c	VRL010	Viral Hepatitis	52	0.363

278	P	CRD246	Cardiovascular System Disease	55	0.363

279		CRH001	Crohn's Disease	80	0.363

280	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	58	0.349

281		HMR039	Hemorrhage, Intracerebral	57	0.349

282		EPD002	Epidermolytic Hyperkeratosis	55	0.349

283		CYT014	Cytochrome P450 Oxidoreductase Deficiency	35	0.349

284		48X005	48,xyyy	39	0.349

285	P	ATS411	Autosomal Dominant Epidermolytic Ichthyosis	37	0.349

286		PSD088	Pseudobulbar Affect	33	0.349

287	P	CRB088	Cerebral Atrophy	32	0.349

288		ORL015	Oral Squamous Cell Carcinoma	43	0.334

289	P	SCH015	Schizophrenia	74	0.334

290		ATH013	Atherosclerosis Susceptibility	63	0.334

291	P	SPR120	Supranuclear Palsy, Progressive, 1	68	0.334

292	P	KLZ004	Kala-Azar 1	41	0.334

293		AVN001	Avian Influenza	61	0.334

294		LSH001	Leishmaniasis	63	0.334

295	P	HYP076	Hyperthyroidism	53	0.334

296		ORL011	Oral Cancer	60	0.334

297		DFC004	Deficiency Anemia	74	0.319

298		BLM002	Bulimia Nervosa	56	0.319

299		CTN028	Cutaneous Telangiectasia and Cancer Syndrome, Familial	70	0.319

300	P	TMR010	Tumor Predisposition Syndrome	69	0.319

301	P	HYP086	Hypothyroidism	68	0.319

302	P	CNT009	Central Core Myopathy	44	0.319

303	P	RTN016	Retinal Degeneration	52	0.319

304	P	THY032	Thyroiditis	56	0.319

305		MLT028	Multiminicore Disease	44	0.319

306		CRT033	Corticobasal Degeneration	48	0.319

307		INH023	Inherited Cancer-Predisposing Syndrome	53	0.319

308		MTC207	Mitochondrial Complex Ii Deficiency, Nuclear Type 1	57	0.302

309	c	MCL042	Macular Degeneration, Age-Related, 1	84	0.302

310	c	LKM061	Leukemia, Acute Myeloid	83	0.302

311		SNL009	Senile Plaque Formation	28	0.302

312		HML010	Hemolytic Anemia Due to Glutathione Reductase Deficiency	21	0.302

313	c	HMC039	Hemochromatosis, Type 1	73	0.302

314	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.302

315		NND010	Nondisjunction	34	0.302

316	P	NML001	Nemaline Myopathy	49	0.302

317		DSS008	Disease of Mental Health	74	0.302

318		IRN001	Iron Deficiency Anemia	58	0.302

319		HMG005	Hemoglobinopathy	55	0.302

320	P	HYD006	Hydrocephalus	62	0.302

321	c	PRM005	Primary Hyperparathyroidism	59	0.302

322	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	62	0.285

323	c	CRB193	Cerebral Amyloid Angiopathy, App-Related	55	0.285

324		ACY009	Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of	58	0.285

325		PRN011	Pernicious Anemia	52	0.285

326		ANX010	Anxiety	70	0.285

327	c	TYP008	Type 1 Diabetes Mellitus	77	0.285

328		HSH003	Hashimoto Thyroiditis	60	0.285

329	c	MYS052	Myasthenic Syndrome, Congenital, 10	46	0.285

330	c	PRG094	Paragangliomas 5	29	0.285

331		PRT019	Protein-Losing Enteropathy	44	0.285

332		PPL002	Papillary Carcinoma	46	0.285

333	P	VSC007	Vascular Disease	62	0.285

334	P	HRM001	Hermansky-Pudlak Syndrome	65	0.285

335	P	KDN018	Kidney Disease	71	0.285

336		MCR017	Macrocytic Anemia	44	0.285

337		GST033	Gestational Diabetes	60	0.285

338		DYS004	Dyscalculia	35	0.285

339		PLC008	Placenta Disease	48	0.285

340		ULC004	Ulcerative Colitis	74	0.285

341		HRD031	Hereditary Paraganglioma-Pheochromocytoma Syndromes	61	0.285

342	P	ALP008	Alopecia	53	0.285

343		MDM001	Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency	34	0.285

344		CRB090	Cerebral Hypoxia	42	0.285

345		HDN002	Head Injury	44	0.285

346		MTH047	Methanol Poisoning	37	0.285

347		WRT005	Warty Dyskeratoma	16	0.285

348	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	66	0.267

349		MYS057	Myasthenic Syndrome, Congenital, 11, Associated with Acetylcholine Receptor Deficiency	38	0.267

350		PYR012	Pyruvate Dehydrogenase E1-Beta Deficiency	40	0.267

351	P	LNG064	Lung Cancer Susceptibility 3	69	0.267

352		NMN001	Nominal Aphasia	40	0.267

353	P	EYD002	Eye Disease	57	0.267

354		TRN015	Transient Cerebral Ischemia	62	0.267

355		MDD011	Mood Disorder	61	0.267

356	P	SBS003	Substance Abuse	54	0.267

357		NDL007	Nodular Goiter	48	0.267

358		CRB004	Cerebral Artery Occlusion	45	0.267

359		TLN003	Telangiectasis	51	0.267

360	P	LCT001	Lactic Acidosis	50	0.267

361		VSC003	Visceral Leishmaniasis	54	0.267

362		DLS001	Delusional Disorder	44	0.267

363		CLT003	Colitis	63	0.247

364	P	CHN044	Chondrodysplasia Punctata Syndrome	43	0.247

365	c	MGR028	Migraine with or Without Aura 1	63	0.247

366	P	OVR042	Ovarian Cancer	88	0.247

367	P	PTY003	Pityriasis Rubra Pilaris	57	0.247

368	c	ALZ050	Alzheimer Disease 5	35	0.247

369		STR095	Structural Heart Defects and Renal Anomalies Syndrome	20	0.247

370		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	58	0.247

371	c	ACT004	Acute Diarrhea	40	0.247

372	P	MYC007	Myocardial Infarction	69	0.247

373	c	NML025	Nemaline Myopathy 8	36	0.247

374		KRN002	Kearns-Sayre Syndrome	62	0.247

375		SQM006	Squamous Cell Carcinoma	59	0.247

376	P	DRR001	Diarrhea	55	0.247

377		LYM027	Lymphopenia	56	0.247

378	P	RHZ001	Rhizomelic Chondrodysplasia Punctata	57	0.247

379		MTH009	Mouth Disease	57	0.247

380		HYP066	Hyperglycemia	60	0.247

381	c	PRC016	Pre-Eclampsia	64	0.247

382		ACT084	Acute Stress Disorder	53	0.247

383		MTC004	Mitochondrial Encephalomyopathy	42	0.247

384		GRN017	Granulocytopenia	42	0.247

385		HMP009	Haemophilus Influenzae	41	0.247

386		GRV012	Grover's Disease	30	0.247

387	c	SVR040	Severe Congenital Nemaline Myopathy	37	0.247

388	c	DNT047	Dentinogenesis Imperfecta Type 2	35	0.247

389		DYS073	Dysphagia	53	0.247

390		PRM329	Premature Aging	36	0.247

391		ORG002	Organic Acidemia	43	0.225

392		MLR004	Malaria	77	0.225

393		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.225

394		MND002	Mandibuloacral Dysplasia with Type B Lipodystrophy	37	0.225

395		ASP007	Aspiration Pneumonia	49	0.225

396		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	0.225

397		ACY005	Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of	54	0.225

398		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	0.225

399	c	NML003	Nemaline Myopathy 2	51	0.225

400		GLT035	Glutaric Acidemia I	57	0.225

401	P	MLT020	Multiple Sclerosis	79	0.225

402	P	D2H002	D-2-Hydroxyglutaric Aciduria 1	53	0.225

403		PLY166	Polyunsaturated Fatty Acids Plasma Level Quantitative Trait Locus 1	8	0.225

404		MYP163	Myopathy, Mitochondrial Progressive, with Congenital Cataract and Developmental Delay	27	0.225

405		DSR012	Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency	39	0.225

406	c	HRM005	Hermansky-Pudlak Syndrome 1	55	0.225

407		FZL002	Fazio-Londe Disease	39	0.225

408	P	RTN008	Retinitis Pigmentosa	79	0.225

409	c	CRD113	Cardiomyopathy, Dilated, 1v	23	0.225

410	P	FRD001	Friedreich Ataxia	62	0.225

411	P	RSP003	Respiratory Failure	73	0.225

412		CHL123	Chlamydia	58	0.225

413		LMB062	Limb Ischemia	55	0.225

414		SVR004	Severe Combined Immunodeficiency	70	0.225

415		NRR001	Neuroretinitis	42	0.225

416		ART014	Articulation Disorder	34	0.225

417		GLC003	Glucose Intolerance	53	0.225

418		SCH014	Schistosomiasis	56	0.225

419		GT001	Gout	63	0.225

420	P	PRN023	Prion Disease	60	0.225

421		RTN023	Retinitis	45	0.225

422	P	DBT009	Diabetes Mellitus	67	0.225

423	P	TXP001	Toxoplasmosis	59	0.225

424		IDP022	Idiopathic Spinal Cord Herniation	17	0.225

425	P	SZR006	Seizure Disorder	69	0.225

426		ANX004	Anoxia	40	0.225

427		CCN001	Cocaine Dependence	47	0.225

428		HRT015	Heritable Pulmonary Arterial Hypertension	46	0.225

429		FML304	Familial Isolated Dilated Cardiomyopathy	50	0.225

430	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	0.225

431		NRM022	Neurometabolic Disease	24	0.225

432		LKP003	Leukoplakia	39	0.225

433		MYP017	Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay	14	0.225

434		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	51	0.202

435	P	ATR011	Atrial Fibrillation	66	0.202

436		DMT001	Dimethylglycine Dehydrogenase Deficiency	27	0.202

437		OPP004	Oppositional Defiant Disorder	48	0.202

438		CRP032	Corpus Callosum, Agenesis of	49	0.202

439		OBS002	Obsessive-Compulsive Disorder	67	0.202

440		MTH026	Methemoglobinemia Due to Deficiency of Methemoglobin Reductase	36	0.202

441		OST159	Osteogenic Sarcoma	66	0.202

442		MTB008	Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration	42	0.202

443		PLY183	Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome	41	0.202

444	c	MCR312	Microphthalmia, Syndromic 10	39	0.202

445		CMB017	Combined Oxidative Phosphorylation Deficiency 6	41	0.202

446	P	ATX030	Ataxia-Telangiectasia	80	0.202

447	P	HYP750	Hypertriglyceridemia, Familial	61	0.202

448		HTT002	Hutterite Cerebroosteonephrodysplasia Syndrome	25	0.202

449		ISV001	Isovaleric Acidemia	54	0.202

450		SDD001	Sudden Infant Death Syndrome	60	0.202

451		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	0.202

452	P	MYS005	Myositis	55	0.202

453		HRW001	Hair Whorl	35	0.202

454		IGR001	Ige Responsiveness, Atopic	58	0.202

455	c	CRT081	Cortical Dysplasia, Complex, with Other Brain Malformations 7	31	0.202

456		TBL035	Tubulinopathy	34	0.202

457		MCR099	Microlissencephaly	39	0.202

458	P	LKM002	Leukemia	65	0.202

459	P	KRT005	Keratoacanthoma	47	0.202

460		OVR063	Overnutrition	42	0.202

461		HYP005	Hypokalemia	55	0.202

462		ANT007	Anterior Horn Cell Disease	31	0.202

463	c	ACT027	Acute Pancreatitis	60	0.202

464	P	ART005	Arteriovenous Malformation	64	0.202

465		CVD001	Covid-19	59	0.202

466		OLG003	Oligohydramnios	50	0.202

467		PLS007	Plasmodium Falciparum Malaria	52	0.202

468		PLR005	Pleuropneumonia	33	0.202

469		NNT010	Nontoxic Goiter	32	0.202

470		CHL004	Cholelithiasis	48	0.202

471		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.202

472		PLY024	Polymicrogyria	48	0.202

473		SNL007	Senile Cataract	40	0.202

474	P	MLG056	Malignant Hyperthermia	65	0.202

475	P	HYP120	Hypoaldosteronism	33	0.202

476	P	SCK005	Sickle Cell Disease	56	0.202

477		CRT015	Carotid Artery Occlusion	45	0.202

478	P	TRM003	Tremor	50	0.202

479		SMN008	Semantic Dementia	46	0.202

480	P	HDC001	Headache	56	0.202

481	c	NMN014	Niemann-Pick Disease, Type C2	49	0.175

482		PRL023	Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome	48	0.175

483		DMN031	Dementia, Lewy Body	65	0.175

484	c	DWL002	Dowling-Degos Disease 1	58	0.175

485	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	79	0.175

486		DHY010	Dihydrolipoamide Dehydrogenase Deficiency	48	0.175

487		MSC157	Muscular Dystrophy, Duchenne Type	78	0.175

488		PYR022	Pyruvate Dehydrogenase E1-Alpha Deficiency	63	0.175

489		ALC007	Alcohol Dependence	65	0.175

490	c	BRN108	Branchiootic Syndrome 1	63	0.175

491		DSM002	Desmosterolosis	39	0.175

492	c	CNG006	Congenital Hypothyroidism	63	0.175

493	P	FML011	Familial Adenomatous Polyposis	70	0.175

494	P	PNC035	Pancreatic Cancer	87	0.175

495		KRT019	Keratitis, Hereditary	66	0.175

496	c	CRB176	Cerebral Amyloid Angiopathy, Itm2b-Related, 1	43	0.175

497		HMC042	Homocystinuria-Megaloblastic Anemia, Cble Complementation Type	34	0.175

498		DHY002	Dihydropyrimidine Dehydrogenase Deficiency	57	0.175

499	P	DNG005	Dengue Virus	55	0.175

500	P	ASP006	Aspergillosis	71	0.175

501		ACR020	Acropectorovertebral Dysplasia	24	0.175

502	P	PRK057	Parkinson Disease, Late-Onset	79	0.175

503		RNL114	Renal Cell Carcinoma, Nonpapillary	79	0.175

504	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	0.175

505	c	RHZ004	Rhizomelic Chondrodysplasia Punctata, Type 3	41	0.175

506	P	SNS001	Sensorineural Hearing Loss	60	0.175

507		TRY001	Trypanosomiasis	50	0.175

508		HMN047	Human Cytomegalovirus Infection	59	0.175

509		SBJ001	Subjective Cognitive Decline	29	0.175

510	P	PLY014	Polycystic Kidney Disease	71	0.175

511	P	HYP111	Hyperprolinemia	44	0.175

512		END040	Endogenous Depression	54	0.175

513		KRT008	Keratopathy	46	0.175

514		VCC001	Vaccinia	49	0.175

515		CCC002	Coccidiosis	50	0.175

516		THY122	Thyroid Gland Cancer	59	0.175

517		CRB037	Cerebral Palsy	66	0.175

518		HMS001	Hemosiderosis	48	0.175

519	P	KLP003	Klippel-Feil Syndrome	47	0.175

520	c	SPN284	Spinocerebellar Ataxia 38	40	0.175

521	P	ALC033	Alcohol Use Disorder	67	0.175

522	P	ECL001	Eclampsia	52	0.175

523		CRB033	Cerebral Degeneration	36	0.175

524		SVR001	Severe Acute Respiratory Syndrome	68	0.175

525		SPN035	Spindle Cell Sarcoma	51	0.175

526		LCL004	Localized Osteosarcoma	35	0.175

527	c	SCN007	Secondary Hyperparathyroidism	50	0.175

528	P	SKN015	Skin Carcinoma	71	0.175

529		HYD001	Hydranencephaly	42	0.175

530		URM002	Uremia	47	0.175

531		CLB002	Clubfoot	50	0.175

532	P	HYP040	Hypospadias	51	0.175

533	P	HYP024	Hypoparathyroidism	55	0.175

534	P	HRD008	Hereditary Hemorrhagic Telangiectasia	64	0.175

535	P	NTR004	Neutropenia	62	0.175

536	P	MTH008	Methylmalonic Acidemia	52	0.175

537	P	ATS308	Autosomal Dominant Cerebellar Ataxia	64	0.175

538		SRC014	Sarcoma	64	0.175

539		PLG002	Plague	58	0.175

540		MTC005	Mitochondrial Metabolism Disease	44	0.175

541	P	MYL006	Myeloid Leukemia	60	0.175

542	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	64	0.175

543	P	ZLL001	Zellweger Syndrome	65	0.175

544	P	BCL017	B-Cell Lymphoma	57	0.175

545	P	INF038	Influenza	68	0.175

546		LNG099	Lung Disease	62	0.175

547	P	INS002	in Situ Carcinoma	52	0.175

548		ERY069	Erythrokeratoderma ''en Cocardes''	26	0.175

549	P	HRP006	Herpes Simplex	65	0.175

550	P	MSC005	Muscular Dystrophy	66	0.175

551		HRN003	Heroin Dependence	44	0.175

552	P	RRH023	Rare Hereditary Hemochromatosis	52	0.175

553	P	RRT020	Rare Tumor	39	0.175

554		MTH046	Methylmalonic Acidemia Without Homocystinuria	39	0.175

555		IDP070	Idiopathic Scoliosis	41	0.143

556	c	CRB098	Cerebrooculofacioskeletal Syndrome 2	30	0.143

557		SXL003	Sexual Disorder	49	0.143

558		AGR018	Agraphia	37	0.143

559	P	PNT019	Pontocerebellar Hypoplasia	45	0.143

560	P	CRB101	Cerebrooculofacioskeletal Syndrome 1	53	0.143

561	c	RHZ011	Rhizomelic Chondrodysplasia Punctata, Type 1	53	0.143

562		CYS001	Cystic Fibrosis	77	0.143

563	P	SRC025	Sarcoidosis 1	70	0.143

564	P	SCL057	Scoliosis, Isolated 1	40	0.143

565	c	SPH013	Spherocytosis, Type 1	42	0.143

566	c	GLY007	Glycogen Storage Disease Iv	58	0.143

567		BTT016	Batten-Turner Congenital Myopathy	54	0.143

568		OCL069	Ocular Motor Apraxia	57	0.143

569		GRS011	Gerstmann-Straussler Disease	56	0.143

570		TLC001	Telecanthus	34	0.143

571		CHR696	Charcot-Marie-Tooth Disease, X-Linked Recessive, 4, with or Without Cerebellar Ataxia	32	0.143

572	P	RTT002	Rett Syndrome	79	0.143

573	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	60	0.143

574		RFS006	Refsum Disease, Classic	63	0.143

575		ADR007	Adrenoleukodystrophy	73	0.143

576		LSC001	Lesch-Nyhan Syndrome	62	0.143

577	c	CTR132	Cataract 3, Multiple Types	41	0.143

578		BRT054	Brittle Bone Disorder	74	0.143

579		SRC015	Sarcosinemia	38	0.143

580	P	PTN014	Patent Ductus Arteriosus 1	59	0.143

581		CHR100	Chronic Ulcer of Skin	57	0.143

582		FML037	Female Breast Cancer	51	0.143

583		VTM002	Vitamin B12 Deficiency	48	0.143

584	c	CRB100	Cerebrooculofacioskeletal Syndrome 4	33	0.143

585		MYP164	Myopathy, Congenital, with Diaphragmatic Defects, Respiratory Insufficiency, and Dysmorphic Facies	24	0.143

586		MYP035	Myopathy, Distal, with Anterior Tibial Onset	33	0.143

587		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	40	0.143

588	P	LSS002	Lissencephaly	52	0.143

589		CRN287	Carnitine Deficiency, Myopathic	17	0.143

590	P	RNL100	Renal Hypodysplasia/aplasia 1	63	0.143

591	P	LNG032	Lung Cancer	98	0.143

592	P	DVL012	Developmental Dysplasia of the Hip 1	45	0.143

593	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	0.143

594		IMM167	Immune Deficiency Disease	76	0.143

595		MYL005	Myelofibrosis	70	0.143

596		PRN056	Parana Hard-Skin Syndrome	17	0.143

597	c	GRV008	Graves Disease 1	54	0.143

598	P	FRG001	Fragile X Syndrome	70	0.143

599		ANM045	Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency	50	0.143

600	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.143

601	c	PNT034	Pontocerebellar Hypoplasia, Type 2e	53	0.143

602		LPT014	Leptin Deficiency or Dysfunction	77	0.143

603	c	BTT014	Beta-Thalassemia	72	0.143

604		CRT072	Creutzfeldt-Jakob Disease	67	0.143

605		PRS012	Pars Planitis	47	0.143

606		CRV035	Cervical Cancer	72	0.143

607		END057	Endometrial Cancer	76	0.143

608		DFF005	Diffuse Large B-Cell Lymphoma	55	0.143

609		OST017	Osteomyelitis	63	0.143

610		NNL006	Non-Alcoholic Steatohepatitis	54	0.143

611		CLR108	Colorectal Adenoma	63	0.143

612		HYP030	Hypoactive Sexual Desire Disorder	40	0.143

613		PHM001	Phimosis	37	0.143

614	c	BSL007	Basal Cell Carcinoma	67	0.143

615	P	PRM002	Primary Hyperoxaluria	65	0.143

616	P	GLY013	Glycogen Storage Disease	59	0.143

617		NNT012	Neonatal Jaundice	53	0.143

618		NRT004	Neuritis	53	0.143

619		IMP005	Impotence	52	0.143

620		DST103	Distal Muscular Dystrophy with Anterior Tibial Onset	29	0.143

621	c	CHR697	Charcot-Marie-Tooth Disease X-Linked Recessive 4	33	0.143

622	P	NRD007	Neurodegeneration with Brain Iron Accumulation	51	0.143

623		DYS003	Dysgraphia	35	0.143

624	P	MVM001	Movement Disease	61	0.143

625		VLK001	Volkmann Contracture	23	0.143

626		SCH012	Schizoaffective Disorder	49	0.143

627	P	DYS154	Dystonia	64	0.143

628	P	MTR014	Motor Neuron Disease	65	0.143

629	P	HRT032	Heart Disease	84	0.143

630		MGL001	Megaloblastic Anemia	59	0.143

631	P	KDN017	Kidney Cancer	60	0.143

632	P	END044	Endometriosis	62	0.143

633	P	ADN016	Adenocarcinoma	63	0.143

634	P	SYS005	Systemic Scleroderma	73	0.143

635		MTS001	Mutism	44	0.143

636		DMY004	Demyelinating Disease	50	0.143

637	P	BRS044	Breast Adenocarcinoma	58	0.143

638		ART016	Aortic Aneurysm	68	0.143

639	P	PNC044	Pancreatitis	61	0.143

640		MRS001	Marasmus	41	0.143

641	P	GRV001	Graves' Disease	54	0.143

642		LST001	Listeriosis	59	0.143

643		MNN009	Meningoencephalitis	47	0.143

644		CHR073	Choreatic Disease	53	0.143

645		RCK004	Rickets	64	0.143

646		BRD004	Borderline Personality Disorder	53	0.143

647		BLS002	Blastomycosis	47	0.143

648	P	GLL022	Guillain-Barre Syndrome	59	0.143

649	P	HRD011	Hereditary Spherocytosis	63	0.143

650	P	UVT001	Uveitis	57	0.143

651		PRM013	Premature Menopause	57	0.143

652		PCD001	Pica Disease	38	0.143

653	P	THR014	Thrombocytopenia	66	0.143

654		HST011	Histoplasmosis	54	0.143

655		CND002	Conduct Disorder	50	0.143

656		SLP001	Sleeping Sickness	56	0.143

657		ATY001	Atypical Depressive Disorder	45	0.143

658		HPT004	Hepatic Coma	43	0.143

659		BRN028	Brain Cancer	73	0.143

660	P	RTN018	Retinal Disease	53	0.143

661		HMG002	Hemoglobinuria	50	0.143

662	P	HML002	Hemolytic Anemia	62	0.143

663		BRS051	Breast Disease	58	0.143

664	P	AXN001	Axonal Neuropathy	33	0.143

665		INH003	Inhibited Female Orgasm	29	0.143

666		DCB001	Decubitus Ulcer	61	0.143

667		AMN002	Amino Acid Metabolic Disorder	40	0.143

668		SBS004	Substance Dependence	46	0.143

669	P	TRC031	Trichorhinophalangeal Syndrome	37	0.143

670		ADR022	Adrenomyeloneuropathy	38	0.143

671		BRN056	Bronchopulmonary Dysplasia	57	0.143

672		FSC004	Fasciitis	49	0.143

673		PRL005	Proliferative Fasciitis	22	0.143

674		CCC003	Coccygodynia	18	0.143

675		GLM045	Glioma	62	0.143

676		ISC003	Ischemic Fasciitis	31	0.143

677	P	HMR005	Hemorrhoid	49	0.143

678		GB1002	Gbe1 Adult Polyglucosan Body Disease	7	0.143

679	c	SBC007	Subacute Thyroiditis	43	0.143

680	c	CHR684	Chronic Kidney Disease	73	0.143

681		ANR040	Aneurysm	60	0.143

682	P	AVS003	Avascular Necrosis	41	0.143

683		PLY100	Polyploidy	36	0.143

684		IDP073	Idiopathic Hypercalciuria	41	0.143

685		GLY078	Glycogen Storage Disease Due to Glycogen Branching Enzyme Deficiency	38	0.143

686		GLL048	Glial Tumor	51	0.143

687	P	RNL123	Renal Agenesis, Bilateral	37	0.143

688		CNG393	Congenital Muscular Dystrophy with Hyperlaxity	12	0.143

689		ASS001	Associative Agnosia	24	0.101

690		HMM004	Hamamy Syndrome	39	0.101

691		ACT119	Acute Promyelocytic Leukemia	62	0.101

692	c	MYP118	Myopathy, Myofibrillar, 8	31	0.101

693	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	0.101

694		ALL003	Allergic Rhinitis	66	0.101

695		ALX002	Alexithymia	36	0.101

696		MCR191	Microscopic Colitis	46	0.101

697		CRH005	Crohn's Colitis	53	0.101

698		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	33	0.101

699	P	CTN015	Cutaneous T Cell Lymphoma	48	0.101

700		FRG008	Fragile X-Associated Tremor/ataxia Syndrome	44	0.101

701	P	PRN026	Porencephaly	54	0.101

702		VLC001	Velocardiofacial Syndrome	57	0.101

703		VRC005	Varicose Veins	59	0.101

704	c	SYS001	Systemic Lupus Erythematosus	85	0.101

705	P	MJR007	Major Affective Disorder 1	42	0.101

706		KRT071	Keratosis, Seborrheic	56	0.101

707		RTN179	Retinal Arteries, Tortuosity of	42	0.101

708	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.101

709	c	GRN062	Granulomatous Disease, Chronic, Autosomal Recessive, 1	46	0.101

710	c	HYD064	Hydrocephalus, Congenital, 1	51	0.101

711		MTC146	Mitochondrial Complex I Deficiency, Nuclear Type 1	59	0.101

712		PLY150	Polykaryocytosis Inducer	29	0.101

713		CRN238	Corneal Dystrophy, Epithelial Basement Membrane	32	0.101

714		CRD002	Cri-Du-Chat Syndrome	50	0.101

715	P	FTL033	Fetal Hemoglobin Quantitative Trait Locus 1	43	0.101

716	P	HYP768	Hyperlipoproteinemia, Type I	67	0.101

717	P	MPL001	Maple Syrup Urine Disease	69	0.101

718		MRD002	Marden-Walker Syndrome	56	0.101

719		DGR001	Digeorge Syndrome	62	0.101

720	c	FNC027	Fanconi Anemia, Complementation Group a	80	0.101

721	P	LNR013	Linear Skin Defects with Multiple Congenital Anomalies 1	52	0.101

722	c	STC015	Stickler Syndrome, Type I	50	0.101

723	P	BLD134	Bladder Cancer	79	0.101

724		STR067	Stroke, Ischemic	79	0.101

725		PRS131	Prostate Cancer/brain Cancer Susceptibility	23	0.101

726		SCK003	Sickle Cell Anemia	74	0.101

727		NRL018	Neural Tube Defects, Folate-Sensitive	46	0.101

728		GND001	Gonadoblastoma	42	0.101

729	P	NSP012	Nasopharyngeal Carcinoma	60	0.101

730		CNZ001	Coenzyme Q10 Deficiency Disease	41	0.101

731		MTC151	Mitochondrial Complex I Deficiency, Nuclear Type 20	37	0.101

732		INT323	Intraocular Pressure Quantitative Trait Locus	63	0.101

733		IFP003	Ifap Syndrome 2	41	0.101

734	c	SPR162	Spermatogenic Failure 50	42	0.101

735	c	FTL067	Fetal Hemoglobin Quantitative Trait Locus 6	25	0.101

736		FSR001	Fusariosis	45	0.101

737		MTH054	Methylmalonic Aciduria and Homocystinuria, Cblc Type	57	0.101

738		FRG010	Fragile X Tremor/ataxia Syndrome	43	0.101

739		ANT042	Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis	37	0.101

740	c	HYP248	Hyperprolinemia, Type I	43	0.101

741		HYP781	Hypoascorbemia	52	0.101

742	P	LPR021	Leprosy 3	71	0.101

743		SPN362	Spondylometaphyseal Dysplasia, Sedaghatian Type	42	0.101

744		SQM013	Squamous Cell Carcinoma, Head and Neck	75	0.101

745		MND023	Mend Syndrome	49	0.101

746		MST021	Meester-Loeys Syndrome	37	0.101

747		TBL029	Tubulin, Beta	28	0.101

748	P	STR020	Strabismus	56	0.101

749		DLY008	Delayed Sleep Phase Disorder	44	0.101

750	c	PRG038	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2	49	0.101

751		GST019	Gastrointestinal Stromal Tumor	78	0.101

752		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.101

753	c	LKM063	Leukemia, Chronic Myeloid	70	0.101

754		CNZ008	Coenzyme Q10 Deficiency, Primary, 6	34	0.101

755	c	PRG040	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4	52	0.101

756		HRS016	Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction	26	0.101

757	P	ANG001	Angelman Syndrome	64	0.101

758		ANT078	Antipyrine Metabolism	24	0.101

759	P	CNR004	Cone-Rod Dystrophy 2	74	0.101

760		MLT157	Multiple System Atrophy 1	69	0.101

761	P	PRG130	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1	54	0.101

762	P	PHC003	Pheochromocytoma	70	0.101

763		GST108	Gist-Plus Syndrome	22	0.101

764	c	CLR041	Colorectal Cancer, Hereditary Nonpolyposis, Type 2	36	0.101

765		EPD015	Epidemic Typhus	44	0.101

766		END014	Endemic Typhus	32	0.101

767		INV001	Invasive Aspergillosis	48	0.101

768		ADR040	Adrenal Gland Pheochromocytoma	45	0.101

769		OST003	Osteonecrosis	60	0.101

770		FWL003	Fowler Urethral Sphincter Dysfunction Syndrome	22	0.101

771		RBS001	Rabies	57	0.101

772		ERY004	Erysipelas	47	0.101

773		LWG006	Low Grade Glioma	41	0.101

774	P	NPH012	Nephrotic Syndrome	61	0.101

775		CLR109	Colorectal Adenocarcinoma	50	0.101

776		SLC006	Silicosis	55	0.101

777		BLP004	Blepharophimosis	36	0.101

778		ASY002	Asymptomatic Neurosyphilis	41	0.101

779	P	LCT002	Lactose Intolerance	51	0.101

780		HDR002	Hidradenitis Suppurativa	54	0.101

781	P	CRN037	Craniosynostosis	67	0.101

782	P	ART021	Arteriosclerosis	53	0.101

783		BLR008	Bilirubin Metabolic Disorder	57	0.101

784	P	THR015	Thrombophilia	51	0.101

785		PPL022	Papilloma	53	0.101

786		RTN020	Retinal Vascular Disease	45	0.101

787	P	BNC003	Bone Cancer	58	0.101

788	P	BRB001	Beriberi	44	0.101

789	P	MLN007	Male Infertility	56	0.101

790		CHL147	Chlamydia Pneumonia	47	0.101

791		STR103	Streptococcus Pneumonia	47	0.101

792		ADJ001	Adjustment Disorder	46	0.101

793		SYS004	Systemic Mastocytosis	62	0.101

794	P	TRN020	Turner Syndrome	67	0.101

795		CLR030	Clear Cell Renal Cell Carcinoma	53	0.101

796	P	HRD200	Hereditary Breast Ovarian Cancer Syndrome	67	0.101

797	P	PRP019	Peripheral Nervous System Disease	57	0.101

798		NTR005	Nutritional Deficiency Disease	60	0.101

799	c	CNT035	Central Nervous System Disease	53	0.101

800		CNG034	Congestive Heart Failure	69	0.101

801	P	HPT021	Hepatitis	68	0.101

802		GST045	Gastroenteritis	58	0.101

803		HYP006	Hypertensive Heart Disease	48	0.101

804		HPT014	Hepatorenal Syndrome	49	0.101

805	P	MYP006	Myopia	55	0.101

806	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	0.101

807	P	URN019	Urinary Tract Infection	48	0.101

808	c	HPT001	Hepatitis C	61	0.101

809	P	ESP024	Esophagitis	60	0.101

810	c	FML021	Familial Hypercholesterolemia	71	0.101

811	P	PLY019	Polyneuropathy	52	0.101

812		SQM002	Squamous Cell Papilloma	45	0.101

813		TYP007	Typhoid Fever	63	0.101

814	P	RHN004	Rhinitis	56	0.101

815		THY030	Thyroid Gland Disease	50	0.101

816	P	GST044	Gastritis	55	0.101

817		PNC129	Pancreatic Adenocarcinoma	64	0.101

818		NCR001	Necrotizing Ulcerative Gingivitis	26	0.101

819		GNG013	Gingivitis	59	0.101

820		SYN005	Synostosis	43	0.101

821		CNN003	Conn's Syndrome	77	0.101

822		PLM010	Pulmonary Edema	54	0.101

823	c	ACT073	Acute Leukemia	59	0.101

824		SPT005	Spotted Fever	49	0.101

825		KRT002	Keratomalacia	54	0.101

826		TTN003	Tetanus	64	0.101

827	c	CHR095	Chronic Progressive External Ophthalmoplegia	48	0.101

828		PRC002	Paracoccidioidomycosis	53	0.101

829		CMM005	Common Cold	55	0.101

830	P	MCR010	Microcephaly	59	0.101

831		TXC005	Toxic Shock Syndrome	61	0.101

832		CHL035	Cholinergic Urticaria	29	0.101

833		AVD001	Avoidant Personality Disorder	49	0.101

834	P	GND004	Gonadal Dysgenesis	46	0.101

835		AZS001	Azoospermia	45	0.101

836		GNG011	Gingival Disease	53	0.101

837	P	URT039	Urticaria	57	0.101

838		DNG003	Dengue Disease	65	0.101

839		BRN026	Branch Retinal Artery Occlusion	41	0.101

840	c	SVR005	Severe Pre-Eclampsia	49	0.101

841	P	MLN008	Melanoma	75	0.101

842	P	INF032	Infertility	60	0.101

843	P	MST009	Mastocytosis	64	0.101

844		ACQ007	Acquired Immunodeficiency Syndrome	58	0.101

845		INV005	Inverted Follicular Keratosis	31	0.101

846		ANT024	Anthrax Disease	57	0.101

847		CHL061	Childhood Leukemia	47	0.101

848		ILS001	Ileus	49	0.101

849		FSC002	Fascioliasis	43	0.101

850	P	MTC133	Mitochondrial Myopathy	51	0.101

851		GSG001	Gas Gangrene	52	0.101

852		PRM020	Premenstrual Tension	39	0.101

853		DVL001	Developmental Coordination Disorder	34	0.101

854		CHR121	Charcot-Marie-Tooth Neuropathy X Type 5	17	0.101

855		PRX001	Peroxisomal Disease	46	0.101

856	P	ENC004	Encephalitis	61	0.101

857		AMB001	Amebiasis	56	0.101

858		MCH006	Mechanical Strabismus	40	0.101

859		YLL002	Yellow Fever	61	0.101

860	P	SDR003	Sideroblastic Anemia	49	0.101

861	P	HYP083	Hypopituitarism	51	0.101

862	P	PLL002	Pellagra	46	0.101

863	P	RTN014	Retinal Artery Occlusion	46	0.101

864	P	MNC007	Monocytic Leukemia	48	0.101

865		CYT002	Cytokine Deficiency	43	0.101

866		HNS001	Hansen's Disease	32	0.101

867		MNN020	Meningococcal Infection	44	0.101

868		MTH021	Methylmalonic Acidemia with Homocystinuria	44	0.101

869		PST021	Postpartum Depression	50	0.101

870		MSL001	Measles	61	0.101

871	P	NRV007	Nervous System Disease	65	0.101

872	P	NRP001	Neuropathy	59	0.101

873		ATS301	Autosomal Dominant Epilepsy with Auditory Features	41	0.101

874		DSR002	Disorders of Intracellular Cobalamin Metabolism	30	0.101

875	P	MTC069	Mitochondrial Disorders	57	0.101

876		NRS003	Neurosyphilis	45	0.101

877	P	MNN013	Meningitis	65	0.101

878		WLL004	Wallerian Degeneration	38	0.101

879		INF118	Inflammatory Myopathy with Abundant Macrophages	27	0.101

880		HRD180	Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome	26	0.101

881		CTS005	Catastrophic Antiphospholipid Syndrome	43	0.101

882		INT075	Intracranial Hypertension	52	0.101

883		ORL012	Oral Leukoplakia	35	0.101

884		PNC049	Pancreatic Adenoma	14	0.101

885		NNT017	Neonatal Adrenoleukodystrophy	51	0.101

886	P	ACT105	Acute Mountain Sickness	52	0.101

887		ADS004	Aids Dementia Complex	39	0.101

888	P	ADT009	Auditory Neuropathy Spectrum Disorder	34	0.101

889		SNK001	Snakebite Envenomation	22	0.101

890		CYN003	Cyanide Poisoning	22	0.101

891		DMN026	Dementia Pugilistica	27	0.101

892		RFR010	Refractory Anemia	49	0.101

893		ARG006	Aregenerative Anemia	28	0.101

894		OST115	Osteonecrosis of the Jaw	40	0.101

895		ADN072	Adenoma of Pancreas	17	0.101

896		DWR001	Dwarfism	44	0.101

897		EXR007	Exercise-Induced Anaphylaxis	24	0.101

898		PST046	Post-Transplant Lymphoproliferative Disease	53	0.101

899		CRB086	Cerebral Aneurysms	40	0.101

900		DVL005	Developmental Dyspraxia	22	0.101

901		SPS057	Spasticity	43	0.101

902		PST092	Posttransplant Acute Limbic Encephalitis	29	0.101

903	c	CHR695	Chronic Primary Adrenal Insufficiency	15	0.101

904		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	44	0.101