Search results for NADP

582 hits were found for NADP

#	Family	MCID	Name	MIFTS	Score
1		GLC009	Glucosephosphate Dehydrogenase Deficiency	53	5.935

2	P	HML002	Hemolytic Anemia	62	5.347

3		HLX001	Helix Syndrome	48	5.192

4		GLM045	Glioma	63	3.693

5		24D001	2,4-Dienoyl-Coa Reductase Deficiency	34	3.422

6		HYP266	Hypoxia	57	3.401

7		GLL048	Glial Tumor	52	3.356

8		FTT001	Fatty Liver Disease	62	3.240

9		PPL052	Papillomatosis, Confluent and Reticulated	34	3.066

10		ANX004	Anoxia	40	2.978

11	P	PLL002	Pellagra	46	2.877

12		GLB002	Glioblastoma	67	2.849

13		HYP066	Hyperglycemia	61	2.827

14		ANM045	Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency	50	2.804

15	P	MYC084	Mycobacterium Tuberculosis 1	68	2.775

16		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	2.668

17		PRT037	Pertussis	65	2.668

18		NNL005	Non-Alcoholic Fatty Liver Disease	63	2.615

19		PST092	Posttransplant Acute Limbic Encephalitis	28	2.553

20		CHL014	Cholera	62	2.553

21	P	HRD144	Hereditary Mixed Polyposis Syndrome	54	2.513

22		MLR004	Malaria	80	2.498

23	P	GLM040	Glioma Susceptibility 1	71	2.493

24		MLG169	Malignant Astrocytoma	57	2.430

25	P	NRB001	Neuroblastoma	66	2.349

26		HMP009	Haemophilus Influenzae	41	2.349

27		HYP056	Hypoglycemia	65	2.297

28		LPT001	Leptospirosis	66	2.182

29	P	TXP001	Toxoplasmosis	60	2.182

30		48X005	48,xyyy	39	2.171

31	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	63	2.149

32		NNT012	Neonatal Jaundice	53	2.103

33	c	LKM061	Leukemia, Acute Myeloid	83	2.079

34		CND006	Candida Glabrata	30	1.981

35	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	1.962

36		INS001	Insulinoma	59	1.962

37		ATH013	Atherosclerosis Susceptibility	63	1.886

38		GRD001	Giardiasis	46	1.886

39	P	CHR012	Chronic Granulomatous Disease	69	1.880

40		CNG017	Congenital Nonspherocytic Hemolytic Anemia	33	1.880

41		47X002	47,xyy	48	1.805

42		ANT024	Anthrax Disease	58	1.805

43		ISC004	Ischemia	61	1.805

44	P	CTR002	Cataract	60	1.781

45	P	MYC008	Myocarditis	59	1.781

46		APP015	Apparent Mineralocorticoid Excess	57	1.773

47	P	TRM004	Trimethylaminuria	45	1.718

48	P	CTN015	Cutaneous T Cell Lymphoma	48	1.718

49	P	PSR002	Psoriasis	63	1.718

50		PST011	Pustulosis of Palm and Sole	52	1.718

51		HYP005	Hypokalemia	55	1.718

52		QFV001	Q Fever	62	1.718

53		DFC004	Deficiency Anemia	74	1.658

54	P	HYP086	Hypothyroidism	69	1.658

55	c	DNT047	Dentinogenesis Imperfecta Type 2	35	1.658

56		VLV047	Volvulus of Midgut	52	1.624

57		OCL069	Ocular Motor Apraxia	57	1.624

58		DBT010	Diabetic Neuropathy	54	1.624

59	P	MSC005	Muscular Dystrophy	67	1.624

60	P	LCT001	Lactic Acidosis	51	1.624

61		CMB083	Combined Immunodeficiency and Megaloblastic Anemia with or Without Hyperhomocysteinemia	28	1.624

62		TXC005	Toxic Shock Syndrome	62	1.624

63	P	MLN008	Melanoma	76	1.624

64		SLP001	Sleeping Sickness	56	1.598

65	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	1.535

66		IRN002	Iron Metabolism Disease	57	1.535

67	P	HYP769	Hyperlysinemia, Type I	42	1.519

68		NRR001	Neuroretinitis	42	1.519

69		RTN023	Retinitis	46	1.519

70	c	RNG015	Ring Chromosome 2	22	1.519

71	P	MYL006	Myeloid Leukemia	61	1.470

72	P	BLD134	Bladder Cancer	79	1.402

73	P	LNG064	Lung Cancer Susceptibility 3	70	1.402

74		LPD008	Lipid Metabolism Disorder	62	1.402

75	c	MCR130	Microvascular Complications of Diabetes 6	41	1.401

76		CMP034	Complete Androgen Insensitivity Syndrome	55	1.401

77	c	MCR120	Microvascular Complications of Diabetes 7	47	1.401

78		PYR009	Pyridoxine Deficiency Anemia	35	1.401

79		RCK004	Rickets	68	1.401

80	c	MCR113	Microvascular Complications of Diabetes 3	52	1.401

81	c	MCR133	Microvascular Complications of Diabetes 4	41	1.401

82		HGH043	High Grade Glioma	45	1.401

83	P	URT039	Urticaria	58	1.401

84		HYP026	Hypoglycemic Coma	37	1.401

85		END057	Endometrial Cancer	72	1.330

86		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	1.330

87		DPH001	Diphtheria	59	1.330

88		HYP060	Hyperinsulinism	54	1.330

89		MSC157	Muscular Dystrophy, Duchenne Type	79	1.260

90	c	CHR708	Chronic Urticaria	42	1.260

91	P	RTN016	Retinal Degeneration	52	1.260

92		HMS001	Hemosiderosis	48	1.260

93		ANP005	Anaplastic Astrocytoma	57	1.260

94		DRM006	Dermatitis	62	1.260

95	P	HYP265	Hypotonia	42	1.260

96		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	1.254

97		MTB004	Metabolic Acidosis	48	1.254

98	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	1.254

99	P	BCL017	B-Cell Lymphoma	59	1.254

100		CHG001	Chagas Disease	66	1.254

101		BLR008	Bilirubin Metabolic Disorder	57	1.254

102	P	HYP076	Hyperthyroidism	53	1.254

103	P	SCK005	Sickle Cell Disease	56	1.254

104		AGN016	Aging	54	1.173

105	P	OVR042	Ovarian Cancer	88	1.173

106	P	PNC035	Pancreatic Cancer	86	1.173

107		OST159	Osteogenic Sarcoma	66	1.173

108		PNC129	Pancreatic Adenocarcinoma	65	1.173

109		TRY001	Trypanosomiasis	50	1.173

110	P	LKM002	Leukemia	67	1.173

111		PNC041	Pancreatic Ductal Adenocarcinoma	51	1.173

112		BRN071	Brain Injury	50	1.173

113	P	ATX030	Ataxia-Telangiectasia	80	1.086

114		DFF005	Diffuse Large B-Cell Lymphoma	54	1.086

115		LKC009	Leukocyte Adhesion Deficiency, Type I	70	1.086

116	P	GST053	Gastric Cancer	83	1.086

117	P	HPT023	Hepatocellular Carcinoma	96	1.086

118		CHL065	Cholangiocarcinoma	58	1.086

119		THY029	Thyroid Carcinoma	51	1.086

120	P	MYP004	Myopathy	67	1.086

121	P	OLG002	Oligodendroglioma	66	1.086

122	P	PLM036	Pulmonary Fibrosis	66	1.086

123		TLN003	Telangiectasis	51	1.086

124	P	ADN016	Adenocarcinoma	63	1.086

125		INT079	Intrahepatic Cholangiocarcinoma	51	1.086

126	P	OVR046	Ovarian Cyst	46	1.086

127	P	ENC018	Encephalopathy	62	1.086

128		DWR001	Dwarfism	44	1.086

129	P	CRC039	Coarctation of Aorta	46	1.076

130		DVR002	Diverticulitis	46	1.076

131	P	RRH023	Rare Hereditary Hemochromatosis	54	1.076

132		PLM001	Pulmonary Tuberculosis	69	1.076

133		VCC001	Vaccinia	47	1.076

134		ADN018	Adenoma	59	1.076

135		CCC002	Coccidiosis	50	1.076

136		CLN015	Colon Adenocarcinoma	65	1.076

137		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	0.991

138	c	ATR087	Atrial Standstill 1	74	0.991

139	P	CLR023	Colorectal Cancer	100	0.991

140		NNL006	Non-Alcoholic Steatohepatitis	54	0.991

141		NRL016	Neural Tube Defects	81	0.991

142		RNL114	Renal Cell Carcinoma, Nonpapillary	80	0.991

143		BCT022	Bacterial Infectious Disease	56	0.991

144		TRM010	Traumatic Brain Injury	51	0.991

145		CHR074	Choriocarcinoma	46	0.991

146	P	LVR013	Liver Disease	69	0.991

147	P	FBR017	Fibrosarcoma	56	0.991

148	P	BRS044	Breast Adenocarcinoma	58	0.991

149		BLD131	Bladder Urothelial Carcinoma	60	0.991

150		PRT036	Peritonitis	65	0.991

151	P	BRB001	Beriberi	44	0.991

152	P	HRT032	Heart Disease	81	0.991

153		PRS045	Prostatic Hypertrophy	53	0.991

154		TRC008	Trachoma	53	0.991

155	P	BNG032	Benign Mesothelioma	53	0.991

156	P	GLM007	Glomerulonephritis	60	0.991

157		CRT066	Cortisone Reductase Deficiency 2	23	0.940

158		PRS129	Prostatic Hyperplasia, Benign	49	0.886

159		SPP011	Suppression of Tumorigenicity 12	61	0.886

160	P	RTN008	Retinitis Pigmentosa	80	0.886

161	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	0.886

162		BTN004	Biotin Deficiency	45	0.886

163		CLT003	Colitis	63	0.886

164		BRN032	Brain Glioma	45	0.886

165	c	HYP602	Hyperoxaluria, Primary, Type Ii	49	0.886

166	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.886

167		ESP021	Esophageal Cancer	83	0.886

168		HRW001	Hair Whorl	35	0.886

169		ORG002	Organic Acidemia	44	0.886

170		SKN019	Skin Melanoma	71	0.886

171		DGN001	Degenerative Disc Disease	49	0.886

172		ALL006	Allergic Asthma	56	0.886

173		CRV038	Cervical Squamous Cell Carcinoma	58	0.886

174		LNG039	Lung Squamous Cell Carcinoma	57	0.886

175		CHL045	Choline Deficiency Disease	39	0.886

176	c	PRC016	Pre-Eclampsia	65	0.886

177		GTR002	Goiter	53	0.886

178		DYS015	Dysentery	50	0.886

179		PRS021	Prostatic Adenoma	43	0.886

180		UTR056	Uterine Corpus Endometrial Carcinoma	27	0.886

181		END075	Endocervical Adenocarcinoma	37	0.886

182	P	PYL005	Pyelonephritis	57	0.886

183	P	PRM002	Primary Hyperoxaluria	65	0.886

184		NRD001	Neurodermatitis	39	0.886

185		RFR010	Refractory Anemia	49	0.768

186	P	CRN300	Coronary Heart Disease 1	73	0.768

187	P	RHM011	Rheumatoid Arthritis	82	0.768

188	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	0.768

189		DGL002	D-Glyceric Aciduria	41	0.768

190	P	PLM037	Pulmonary Hypertension	72	0.768

191	c	MCR115	Microvascular Complications of Diabetes 5	65	0.768

192		MYL009	Myelodysplastic Syndrome	67	0.768

193		MSC007	Muscle Hypertrophy	64	0.768

194	c	2HY001	2-Hydroxyglutaric Aciduria	38	0.768

195	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	0.768

196	c	PCH010	Pachyonychia Congenita 3	43	0.768

197		FRC001	Fructose-1,6-Bisphosphatase Deficiency	50	0.768

198	P	GLC113	Galactosemia I	66	0.768

199		MYL005	Myelofibrosis	71	0.768

200	P	SPP010	Suppressor of Tumorigenicity 3	51	0.768

201	P	SRC025	Sarcoidosis 1	71	0.768

202		PYR041	Pyruvate Kinase Deficiency of Red Cells	57	0.768

203		URT049	Urate Oxidase, Pseudogene	24	0.768

204	c	HYP595	Hypertension, Essential	85	0.768

205	c	TYP009	Type 2 Diabetes Mellitus	92	0.768

206		MLD001	Melioidosis	67	0.768

207		GLC003	Glucose Intolerance	54	0.768

208	c	RTN130	Retinitis Pigmentosa 46	40	0.768

209		FML063	Familial Glucocorticoid Deficiency	58	0.768

210		ACT003	Acute Kidney Tubular Necrosis	46	0.768

211	P	NRP001	Neuropathy	60	0.768

212	P	DBT009	Diabetes Mellitus	67	0.768

213		ULC004	Ulcerative Colitis	74	0.768

214		FDL002	Food Allergy	47	0.768

215	P	EPL164	Epilepsy	68	0.768

216	P	SKN015	Skin Carcinoma	71	0.768

217		GST040	Gastric Adenocarcinoma	67	0.768

218	P	ART022	Arthritis	71	0.768

219	P	PRD008	Periodontitis	64	0.768

220		CRB004	Cerebral Artery Occlusion	45	0.768

221	P	LTR001	Lateral Sclerosis	58	0.768

222	c	ACT027	Acute Pancreatitis	60	0.768

223	P	ECL001	Eclampsia	52	0.768

224		TXC004	Toxic Diffuse Goiter	23	0.768

225		ORN001	Ornithosis	39	0.768

226	c	CNG027	Congenital Hemolytic Anemia	48	0.768

227	P	PNC044	Pancreatitis	61	0.768

228	P	PRP019	Peripheral Nervous System Disease	58	0.768

229		DBT007	Diabetic Cataract	36	0.768

230		CHL068	Cholestasis	61	0.768

231	P	CRD246	Cardiovascular System Disease	56	0.768

232		SQM006	Squamous Cell Carcinoma	60	0.768

233		CLP006	Clopidogrel Resistance	44	0.768

234		CRL001	Cerulean Cataract	26	0.768

235		BRN056	Bronchopulmonary Dysplasia	56	0.768

236		MYX004	Myxedema	43	0.633

237		CRN036	Craniopharyngioma	64	0.633

238	c	BSL007	Basal Cell Carcinoma	68	0.633

239		SNL007	Senile Cataract	40	0.633

240		FRC013	Fructose Utilization	15	0.627

241	P	SMP003	Simpson-Golabi-Behmel Syndrome	49	0.627

242		PLY100	Polyploidy	36	0.627

243		STN013	Stenotrophomonas Maltophilia Infection	26	0.627

244	P	ALZ034	Alzheimer Disease	87	0.627

245	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.627

246	c	GLL024	Gallbladder Disease 1	52	0.627

247	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.627

248	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	0.627

249		ASP030	Aspirin Resistance	40	0.627

250	P	KLZ004	Kala-Azar 1	41	0.627

251	c	PLM164	Pulmonary Hypertension, Primary, 1	76	0.627

252	P	PRK057	Parkinson Disease, Late-Onset	80	0.627

253	c	L2H001	L-2-Hydroxyglutaric Aciduria	49	0.627

254	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.627

255	P	INF037	Inflammatory Bowel Disease	53	0.627

256	P	PLY014	Polycystic Kidney Disease	69	0.627

257		LWG006	Low Grade Glioma	41	0.627

258		BNR002	Bone Resorption Disease	47	0.627

259	P	LYM118	Lymphoma	67	0.627

260	P	SML001	Small Cell Carcinoma	52	0.627

261		URL001	Urolithiasis	46	0.627

262	P	CHN012	Chondrosarcoma	57	0.627

263	P	FRD001	Friedreich Ataxia	61	0.627

264	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	0.627

265	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.627

266	c	BRN108	Branchiootic Syndrome 1	62	0.627

267	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.627

268	P	MCR129	Microvascular Complications of Diabetes 1	68	0.627

269		MYP071	Myopathy Due to Myoadenylate Deaminase Deficiency	43	0.627

270	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.627

271	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.627

272	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.627

273	c	HYD046	Hydatidiform Mole, Recurrent, 1	59	0.627

274		DWN001	Down Syndrome	70	0.627

275	P	RTN024	Retinoblastoma	73	0.627

276		FND001	Fundus Albipunctatus	55	0.627

277	P	HNT016	Huntington Disease	73	0.627

278		PLM129	Pulmonary Disease, Chronic Obstructive	74	0.627

279	P	MYC007	Myocardial Infarction	70	0.627

280		RBF001	Riboflavin Deficiency	49	0.627

281		MNN043	Meningioma, Familial	79	0.627

282		DSS032	Disease by Infectious Agent	55	0.627

283		CLR109	Colorectal Adenocarcinoma	50	0.627

284		ARG004	Argyria	26	0.627

285		PRM329	Premature Aging	36	0.627

286		RFR009	Refractory Cytopenia with Multilineage Dysplasia	30	0.627

287		ANG046	Angioimmunoblastic T-Cell Lymphoma	51	0.627

288	c	ACT073	Acute Leukemia	58	0.627

289	P	OPN001	Open-Angle Glaucoma	55	0.627

290		CNG393	Congenital Muscular Dystrophy with Hyperlaxity	12	0.627

291		CRH001	Crohn's Disease	80	0.627

292	c	CHR684	Chronic Kidney Disease	69	0.627

293		CRC021	Carcinosarcoma	64	0.627

294	P	LCH002	Lichen Planus	54	0.627

295		RSC001	Rosacea	55	0.627

296		INT040	Intrinsic Asthma	36	0.627

297	P	HRP006	Herpes Simplex	65	0.627

298		LSH001	Leishmaniasis	64	0.627

299		GST010	Gestational Trophoblastic Neoplasm	52	0.627

300		HGH041	High-Grade Astrocytoma	36	0.627

301		ACT168	Acute Annular Outer Retinopathy	10	0.627

302		SKN016	Skin Disease	63	0.627

303	P	OPT006	Optic Nerve Disease	58	0.627

304	P	OLV001	Olivopontocerebellar Atrophy	51	0.627

305	P	GST044	Gastritis	55	0.627

306		ART016	Aortic Aneurysm	68	0.627

307	P	ACN011	Acne	57	0.627

308		CLR030	Clear Cell Renal Cell Carcinoma	54	0.627

309	P	BNG002	Benign Meningioma	36	0.627

310		SCR001	Secretory Meningioma	40	0.627

311		LYM002	Lymphoplasmacyte-Rich Meningioma	35	0.627

312		CHL061	Childhood Leukemia	47	0.627

313	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.627

314		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.627

315		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	0.627

316	c	MCR112	Microvascular Complications of Diabetes 2	42	0.627

317		GT001	Gout	64	0.627

318		CNN003	Conn's Syndrome	79	0.627

319		ALC006	Alcoholic Hepatitis	61	0.627

320		RYS001	Reye Syndrome	49	0.627

321		KRT009	Keratosis	53	0.627

322		IRN001	Iron Deficiency Anemia	58	0.627

323	P	CRD119	Cardiac Arrest	67	0.627

324		CHL123	Chlamydia	58	0.627

325	P	PRN023	Prion Disease	60	0.627

326	c	INH020	Inherited Metabolic Disorder	48	0.627

327		BRS099	Breast Ductal Carcinoma	61	0.627

328	P	ART021	Arteriosclerosis	54	0.627

329	P	PLY019	Polyneuropathy	52	0.627

330		DBT002	Diabetic Autonomic Neuropathy	41	0.627

331		SPN021	Spinal Meningioma	50	0.627

332		TLR001	Tularemia	56	0.627

333		HST011	Histoplasmosis	55	0.627

334	P	ICH004	Ichthyosis	56	0.627

335		STM007	Stomatitis	54	0.627

336	c	KCN020	Kcnt1-Related Epilepsy	13	0.627

337		ANR040	Aneurysm	61	0.627

338		ALL014	Allergic Encephalomyelitis	34	0.627

339	P	SPN237	Spina Bifida Aperta	19	0.443

340	P	OTT001	Otitis Externa	42	0.443

341	c	BCT007	Bacterial Meningitis	55	0.443

342		PRQ002	Paraquat Poisoning	28	0.443

343		HVY003	Heavy Chain Deposition Disease	17	0.443

344	c	INH030	Inherited Retinal Disorder	28	0.443

345	c	SPS035	Spastic Paraplegia 29	13	0.443

346	P	THL005	Thalassemia	56	0.443

347	c	ACT134	Acute Liver Failure	59	0.443

348	P	NSP012	Nasopharyngeal Carcinoma	61	0.443

349		MTH071	Methane Production	25	0.443

350		DHY002	Dihydropyrimidine Dehydrogenase Deficiency	57	0.443

351		PHS014	Phosphoglycerate Kinase 1 Deficiency	45	0.443

352	c	THY107	Thymoma, Familial	42	0.443

353		TRC120	Tricarboxylic Acid Cycle, Defect of	16	0.443

354		LSC001	Lesch-Nyhan Syndrome	62	0.443

355		MST021	Meester-Loeys Syndrome	42	0.443

356	P	WSK001	Wiskott-Aldrich Syndrome	72	0.443

357	P	LPR021	Leprosy 3	71	0.443

358		LPD012	Lipoid Congenital Adrenal Hyperplasia	70	0.443

359		ANN002	Anencephaly	57	0.443

360	P	AST005	Asthma	76	0.443

361	c	PRK090	Parkinson Disease 3, Autosomal Dominant	38	0.443

362		ONC007	Oncocytoma	50	0.443

363	P	D2H002	D-2-Hydroxyglutaric Aciduria 1	52	0.443

364		HMC014	Homocysteinemia	52	0.443

365		CRV035	Cervical Cancer	73	0.443

366		ANX010	Anxiety	70	0.443

367		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	0.443

368	P	SCH015	Schizophrenia	74	0.443

369		HRD029	Hereditary Leiomyomatosis and Renal Cell Cancer	56	0.443

370	P	PHC003	Pheochromocytoma	69	0.443

371	P	LKM071	Leukemia, Chronic Lymphocytic	75	0.443

372	c	TBL031	Tubulointerstitial Kidney Disease, Autosomal Dominant, 1	47	0.443

373		CLF027	Cleft Palate, Isolated	64	0.443

374		CRT072	Creutzfeldt-Jakob Disease	68	0.443

375		ATM095	Autoimmune Disease	61	0.443

376	P	BRS047	Breast Cancer	98	0.443

377		ALC007	Alcohol Dependence	66	0.443

378	c	MST023	Mesothelioma, Malignant	56	0.443

379	P	ANT080	Antigen Defined by Monoclonal Antibody Aj9	18	0.443

380	c	MGR028	Migraine with or Without Aura 1	64	0.443

381		OTT002	Otitis Media	71	0.443

382	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	59	0.443

383		CYS001	Cystic Fibrosis	78	0.443

384	P	HYP605	Hyperphenylalaninemia, Bh4-Deficient, B	44	0.443

385		ATM096	Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia	65	0.443

386	P	APL001	Aplastic Anemia	73	0.443

387		ALC001	Alcohol-Related Birth Defect	36	0.443

388	P	FML011	Familial Adenomatous Polyposis	71	0.443

389	P	EXN002	Exanthem	58	0.443

390		HYP001	Hypochromic Microcytic Anemia	37	0.443

391		FML037	Female Breast Cancer	51	0.443

392		ATS010	Autosomal Recessive Disease	42	0.443

393		ECT041	Ectodermal Dysplasia-Syndactyly Syndrome 2	36	0.443

394	c	D2H003	D-2-Hydroxyglutaric Aciduria 2	35	0.443

395	c	BTT014	Beta-Thalassemia	72	0.443

396	P	PRK101	Parkinsonism-Dystonia, Infantile, 1	40	0.443

397	P	FST017	Fasting Plasma Glucose Level Quantitative Trait Locus 5	12	0.443

398		CYN002	Cyanosis, Transient Neonatal	43	0.443

399		KSH001	Keshan Disease	34	0.443

400		KSH004	Kashin-Beck Disease	38	0.443

401	P	HYP111	Hyperprolinemia	45	0.443

402		CVD001	Covid-19	57	0.443

403		ACT098	Acute Erythroid Leukemia	55	0.443

404	P	URN019	Urinary Tract Infection	49	0.443

405		MYL020	Myelomeningocele	51	0.443

406		GLC086	Glucocorticoid-Induced Osteoporosis	43	0.443

407		CRH005	Crohn's Colitis	53	0.443

408		HYP025	Hyperphosphatemia	48	0.443

409	c	PRM032	Primary Congenital Glaucoma	41	0.443

410	P	FTL001	Fetal Alcohol Syndrome	55	0.443

411		CLR108	Colorectal Adenoma	64	0.443

412		HLC007	Helicobacter Pylori Infection	67	0.443

413	c	MCR245	Microphthalmia, Syndromic 8	46	0.443

414	c	BRT028	Brittle Cornea Syndrome 1	39	0.443

415		IMM167	Immune Deficiency Disease	78	0.443

416	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	0.443

417		GRG001	Greig Cephalopolysyndactyly Syndrome	64	0.443

418		PRP001	Propionic Acidemia	65	0.443

419	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.443

420	c	NPH068	Nephronophthisis 16	43	0.443

421	P	STN012	Sting-Associated Vasculopathy, Infantile-Onset	42	0.443

422		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	39	0.443

423		INT323	Intraocular Pressure Quantitative Trait Locus	64	0.443

424	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	55	0.443

425	c	DFN134	Deafness, Autosomal Dominant 40	22	0.443

426	c	DFN360	Deafness, Autosomal Dominant 69	34	0.443

427		HMM004	Hamamy Syndrome	39	0.443

428		ADR042	Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency	50	0.443

429	c	GLC079	Glaucoma 1, Open Angle, P	23	0.443

430	P	MPL001	Maple Syrup Urine Disease	70	0.443

431		RHM035	Rheumatic Fever-Related Antigen	37	0.443

432		BLD065	Blue Diaper Syndrome	20	0.443

433		HRT031	Hartnup Disorder	52	0.443

434		HMC042	Homocystinuria-Megaloblastic Anemia, Cble Complementation Type	33	0.443

435		HYD030	Hydroxykynureninuria	27	0.443

436	c	PRD040	Periodontitis, Chronic	52	0.443

437		PHN003	Phenylketonuria	76	0.443

438	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	0.443

439		GLB001	Gilbert Syndrome	53	0.443

440	P	HYP750	Hypertriglyceridemia, Familial	62	0.443

441	P	MDL005	Medulloblastoma	75	0.443

442	c	HYP731	Hyperaldosteronism, Familial, Type I	58	0.443

443	c	SPS094	Spastic Paraplegia 29, Autosomal Dominant	28	0.443

444	c	HYP326	Hyperinsulinemic Hypoglycemia, Familial, 5	51	0.443

445	c	HYP271	Hyperinsulinemic Hypoglycemia, Familial, 4	53	0.443

446	c	HYP807	Hyperinsulinemic Hypoglycemia, Familial, 6	52	0.443

447	c	NMN014	Niemann-Pick Disease, Type C2	49	0.443

448		ADR040	Adrenal Gland Pheochromocytoma	46	0.443

449		RNL077	Renal Fibrosis	46	0.443

450		ATS251	Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna	38	0.443

451		CRT020	Cortisone Reductase Deficiency	34	0.443

452		STN011	Sting-Associated Vasculopathy with Onset in Infancy	45	0.443

453		LBR036	Leber Plus Disease	66	0.443

454		ICH054	Ichthyosis, X-Linked	52	0.443

455	c	ATS013	Autosomal Recessive Congenital Ichthyosis	66	0.443

456		FCL090	Facial Cleft	30	0.443

457		RPD005	Rapidly Involuting Congenital Hemangioma	46	0.443

458	P	ZLL001	Zellweger Syndrome	65	0.443

459	P	MSC003	Muscular Atrophy	52	0.443

460		PLM014	Pleomorphic Adenoma	51	0.443

461		MCP006	Mucoepidermoid Carcinoma	48	0.443

462		EXT007	Extracutaneous Mastocytoma	38	0.443

463		PRS042	Prostate Disease	42	0.443

464		SCR011	Scrapie	39	0.443

465		URT010	Ureteral Obstruction	45	0.443

466		VSC003	Visceral Leishmaniasis	55	0.443

467	P	HMC002	Homocystinuria	53	0.443

468		CLF001	Cleft Lip	53	0.443

469	P	ATR005	Atrophic Gastritis	50	0.443

470		AMB001	Amebiasis	57	0.443

471		VRL011	Viral Infectious Disease	61	0.443

472	P	MLG056	Malignant Hyperthermia	66	0.443

473		CHC001	Chickenpox	57	0.443

474		LPD009	Lipid Storage Disease	45	0.443

475		FND002	Fundus Dystrophy	55	0.443

476	c	CHR688	Chronic Acquired Demyelinating Polyneuropathy	16	0.443

477		ACT162	Acute Sensory Ataxic Neuropathy	24	0.443

478	P	HYP098	Hypereosinophilic Syndrome	66	0.443

479	P	MTH008	Methylmalonic Acidemia	52	0.443

480	P	CYS018	Cystitis	59	0.443

481		MST004	Mast Cell Neoplasm	42	0.443

482	c	VRL010	Viral Hepatitis	53	0.443

483		TRC003	Trichomoniasis	53	0.443

484		TRT001	Teratocarcinoma	42	0.443

485	P	CND004	Candidiasis	58	0.443

486		LNG031	Lung Benign Neoplasm	51	0.443

487	P	SYS005	Systemic Scleroderma	74	0.443

488		ADR005	Adrenal Carcinoma	62	0.443

489	P	RNL017	Renal Oncocytoma	54	0.443

490		ACQ007	Acquired Immunodeficiency Syndrome	59	0.443

491	P	INF038	Influenza	68	0.443

492		NRM005	Neuromuscular Disease	63	0.443

493		PPT005	Peptic Ulcer Disease	58	0.443

494		EBL001	Ebola Hemorrhagic Fever	56	0.443

495	P	PLC011	Pilocytic Astrocytoma	57	0.443

496	P	MNC007	Monocytic Leukemia	47	0.443

497	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.443

498		VSL013	Visual Impairment and Progressive Phthisis Bulbi	36	0.443

499	P	SNS001	Sensorineural Hearing Loss	59	0.443

500		THY006	Thymus Lymphoma	27	0.443

501		LGN002	Legionellosis	62	0.443

502	P	DMN002	Dementia	66	0.443

503	P	HYP061	Hypertrophic Cardiomyopathy	69	0.443

504		ALL029	Allergic Disease	59	0.443

505		VRC001	Varicocele	48	0.443

506		FLR001	Filarial Elephantiasis	59	0.443

507		PRN009	Paranoid Schizophrenia	49	0.443

508		PRM236	Primary Biliary Cholangitis	60	0.443

509	c	ACT068	Acute Cystitis	61	0.443

510		SCK001	Sick Building Syndrome	33	0.443

511	P	VSC007	Vascular Disease	63	0.443

512		SNS003	Sensory Peripheral Neuropathy	52	0.443

513	P	DDN001	Duodenal Ulcer	53	0.443

514	P	NMN002	Niemann-Pick Disease	60	0.443

515	P	NPH005	Nephronophthisis	56	0.443

516	P	GCH001	Gaucher's Disease	70	0.443

517		DRG002	Drug-Induced Hepatitis	42	0.443

518	P	KRN004	Kernicterus	46	0.443

519		TST014	Testicular Cancer	52	0.443

520		ACT078	Acute Porphyria	49	0.443

521		MGL001	Megaloblastic Anemia	58	0.443

522		SCH014	Schistosomiasis	56	0.443

523		PRS036	Parasitic Protozoa Infectious Disease	44	0.443

524		GST033	Gestational Diabetes	61	0.443

525	P	RNL015	Renal Hypertension	45	0.443

526		FLR002	Filariasis	55	0.443

527	P	HYD006	Hydrocephalus	61	0.443

528		NPH010	Nephrosclerosis	50	0.443

529		ONC002	Onchocerciasis	51	0.443

530	P	HYP024	Hypoparathyroidism	55	0.443

531		MCR018	Microcytic Anemia	47	0.443

532		CNG034	Congestive Heart Failure	69	0.443

533		RCT015	Reactive Arthritis	61	0.443

534		LMY003	Leiomyomatosis	44	0.443

535	P	INF032	Infertility	57	0.443

536	P	SLP005	Sleep Disorder	61	0.443

537	P	PNM007	Pneumonia	67	0.443

538		INT020	Intravenous Leiomyomatosis	36	0.443

539		CRT015	Carotid Artery Occlusion	45	0.443

540		PLM029	Palmoplantar Keratosis	48	0.443

541	P	CYS039	Cystic Kidney Disease	53	0.443

542	P	THY023	Thymoma	64	0.443

543		PSD007	Pseudomyxoma Peritonei	53	0.443

544	P	TMP001	Temporal Lobe Epilepsy	49	0.443

545	c	FML021	Familial Hypercholesterolemia	72	0.443

546		MSN003	Mesenteric Vascular Occlusion	24	0.443

547		TYP007	Typhoid Fever	64	0.443

548	P	PRP029	Porphyria	60	0.443

549		PLS007	Plasmodium Falciparum Malaria	52	0.443

550	P	ADL010	Adult Respiratory Distress Syndrome	71	0.443

551		LST001	Listeriosis	59	0.443

552		CTS002	Cat-Scratch Disease	42	0.443

553		RHM001	Rheumatic Fever	59	0.443

554		LYM021	Lymphadenitis	56	0.443

555	P	OVR049	Ovarian Disease	52	0.443

556		LCH001	Leech Infestation	38	0.443

557		CHR073	Choreatic Disease	54	0.443

558		NNT010	Nontoxic Goiter	32	0.443

559		HYP014	Hyperuricemia	51	0.443

560		BBS001	Babesiosis	49	0.443

561		ALB002	Albinism	47	0.443

562	P	MNN013	Meningitis	65	0.443

563	c	JVN010	Juvenile Rheumatoid Arthritis	66	0.443

564		PRM209	Primary Trimethylaminuria	19	0.443

565		DRG003	Drug Dependence	46	0.443

566	c	NNS007	Nonsyndromic Deafness	33	0.443

567		HNS001	Hansen's Disease	32	0.443

568		HYP835	Hypothalamic Obesity	38	0.443

569		PTT041	Pituitary Stalk Interruption Syndrome	54	0.443

570		WLL004	Wallerian Degeneration	38	0.443

571		CNG486	Congenital Disorders of N-Linked Glycosylation and Multiple Pathway	29	0.443

572		RFC001	Rfc1 Canvas / Spectrum Disorder	5	0.443

573		AGR019	Age-Related Hearing Loss	41	0.443

574		CYT002	Cytokine Deficiency	43	0.443

575	c	CNG216	Congenital Hydrocephalus	53	0.443

576		CHR178	Chromosomal Triplication	34	0.443

577		HVY002	Heavy Metal Poisoning	22	0.443

578		MTH046	Methylmalonic Acidemia Without Homocystinuria	39	0.443

579		OVR094	Ovarian Epithelial Cancer	39	0.443

580		CRC006	Carcinoid Syndrome	55	0.443

581		FST010	Fasting Hypoglycemia	33	0.443

582		GLC039	Glucosephosphate Isomerase Deficiency	17	0.443