Search results for Chondroitin

517 hits were found for Chondroitin

#	Family	MCID	Name	MIFTS	Score
1		BRC115	Brachyolmia Type 1, Toledo Type	14	4.145

2		OST012	Osteoarthritis	78	0.531

3	P	CYS018	Cystitis	59	0.230

4		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.218

5	P	INT143	Interstitial Cystitis	61	0.207

6		SPN186	Spinal Cord Injury	60	0.207

7	P	CHN012	Chondrosarcoma	56	0.201

8	P	MLN008	Melanoma	69	0.147

9	P	ART023	Arthropathy	62	0.137

10	P	ART022	Arthritis	69	0.130

11		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.130

12	P	GLM045	Glioma	63	0.123

13		ATH013	Atherosclerosis Susceptibility	65	0.120

14	P	NRB001	Neuroblastoma	72	0.116

15	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	69	0.116

16		SYN007	Synovitis	54	0.112

17		PLC002	Plica Syndrome	36	0.112

18	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.108

19		GLL048	Glial Tumor	45	0.108

20		GLB015	Glioblastoma Multiforme	75	0.104

21	c	ACT068	Acute Cystitis	63	0.104

22	c	PNS012	Paine Syndrome	61	0.104

23		MST004	Mast Cell Neoplasm	42	0.104

24		EXT007	Extracutaneous Mastocytoma	38	0.104

25	c	CFF010	Coffin-Siris Syndrome 3	42	0.099

26	P	PSR002	Psoriasis	62	0.095

27		PST011	Pustulosis of Palm and Sole	52	0.095

28		DGN001	Degenerative Disc Disease	48	0.095

29	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.095

30	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.090

31		LWC001	Low Compliance Bladder	43	0.085

32	P	BRS047	Breast Cancer	97	0.079

33	P	MSC005	Muscular Dystrophy	66	0.079

34	P	NRP001	Neuropathy	56	0.079

35		CRT017	Cartilage Disease	54	0.079

36	c	EXS019	Exostoses, Multiple, Type I	53	0.079

37		PLS007	Plasmodium Falciparum Malaria	52	0.079

38		KSH004	Kashin-Beck Disease	38	0.079

39	P	OVR042	Ovarian Cancer	88	0.073

40		MLR004	Malaria	81	0.073

41		SPN209	Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations	66	0.073

42	P	HRP006	Herpes Simplex	65	0.073

43		HYP066	Hyperglycemia	61	0.073

44		TRM010	Traumatic Brain Injury	51	0.073

45		BRN071	Brain Injury	49	0.073

46		SKL017	Skeletal Dysplasias	40	0.073

47		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.073

48	P	CLR023	Colorectal Cancer	99	0.067

49	P	OST002	Osteoporosis	74	0.067

50	c	MCP052	Mucopolysaccharidosis, Type Vi	67	0.067

51		GST092	Gastroesophageal Reflux	67	0.067

52		OST159	Osteogenic Sarcoma	66	0.067

53		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.067

54	P	PRD008	Periodontitis	64	0.067

55		ATM095	Autoimmune Disease	62	0.067

56		EYD002	Eye Disease	58	0.067

57		IRN002	Iron Metabolism Disease	57	0.067

58		PNG002	Pain Agnosia	51	0.067

59		BNR002	Bone Resorption Disease	48	0.067

60	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.067

61	P	BNG032	Benign Mesothelioma	46	0.067

62		DWR001	Dwarfism	44	0.067

63	P	END039	Endodermal Sinus Tumor	44	0.067

64	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.067

65		TST018	Testicular Yolk Sac Tumor	39	0.067

66	c	CHR087	Chronic Cystitis	34	0.067

67		RDT001	Radiation Cystitis	32	0.067

68	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.060

69		CRH001	Crohn's Disease	74	0.060

70		ULC004	Ulcerative Colitis	73	0.060

71	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.060

72		MSC157	Muscular Dystrophy, Duchenne Type	72	0.060

73	P	MLT020	Multiple Sclerosis	72	0.060

74	P	PHC003	Pheochromocytoma	71	0.060

75		DFC004	Deficiency Anemia	70	0.060

76	P	AMY004	Amyloidosis	70	0.060

77	P	ADN016	Adenocarcinoma	64	0.060

78		SKN016	Skin Disease	63	0.060

79		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.060

80	P	FBR017	Fibrosarcoma	56	0.060

81	P	INF037	Inflammatory Bowel Disease	54	0.060

82	P	LTR001	Lateral Sclerosis	54	0.060

83	P	AST007	Astrocytoma	51	0.060

84		TMT002	Temtamy Preaxial Brachydactyly Syndrome	50	0.060

85		ADR040	Adrenal Gland Pheochromocytoma	46	0.060

86		URT010	Ureteral Obstruction	45	0.060

87		URL001	Urolithiasis	45	0.060

88		CYT002	Cytokine Deficiency	42	0.060

89		BCK006	Back Pain	42	0.060

90		ALL014	Allergic Encephalomyelitis	38	0.060

91		MCP033	Mucopolysaccharidoses	38	0.060

92	P	HPT023	Hepatocellular Carcinoma	100	0.052

93	P	ALZ034	Alzheimer Disease	88	0.052

94	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.052

95	P	KDN018	Kidney Disease	72	0.052

96	P	LKM002	Leukemia	68	0.052

97		CST001	Costello Syndrome	68	0.052

98		CNN005	Connective Tissue Disease	68	0.052

99		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.052

100	P	HYD006	Hydrocephalus	66	0.052

101		KRT019	Keratitis, Hereditary	65	0.052

102		PRT036	Peritonitis	64	0.052

103		NRM005	Neuromuscular Disease	64	0.052

104	P	MST009	Mastocytosis	64	0.052

105	P	CRN300	Coronary Heart Disease 1	63	0.052

106	c	GLC092	Glaucoma, Primary Open Angle	62	0.052

107	P	ESP024	Esophagitis	62	0.052

108		ALL026	Allergic Hypersensitivity Disease	62	0.052

109	P	MYL006	Myeloid Leukemia	60	0.052

110	P	BCL017	B-Cell Lymphoma	58	0.052

111		FBR047	Fibromyalgia	58	0.052

112	P	URT039	Urticaria	58	0.052

113		DSS008	Disease of Mental Health	58	0.052

114		HYP266	Hypoxia	57	0.052

115	P	PLY019	Polyneuropathy	56	0.052

116		CHR100	Chronic Ulcer of Skin	55	0.052

117		SNS003	Sensory Peripheral Neuropathy	54	0.052

118		PRS045	Prostatic Hypertrophy	53	0.052

119	P	RTN016	Retinal Degeneration	53	0.052

120	c	PSR017	Psoriasis 2	53	0.052

121	c	MCR113	Microvascular Complications of Diabetes 3	52	0.052

122	c	PSR023	Psoriasis 1	52	0.052

123		PPT001	Peptic Esophagitis	52	0.052

124		PRS021	Prostatic Adenoma	51	0.052

125		CLR109	Colorectal Adenocarcinoma	51	0.052

126	P	OVR082	Overgrowth Syndrome	50	0.052

127	P	TMP001	Temporal Lobe Epilepsy	50	0.052

128		KRT001	Keratoconjunctivitis Sicca	49	0.052

129		PRS129	Prostatic Hyperplasia, Benign	49	0.052

130	P	OPN001	Open-Angle Glaucoma	49	0.052

131		BLD044	Bladder Disease	48	0.052

132	c	PSR032	Psoriasis 11	47	0.052

133	c	MCR120	Microvascular Complications of Diabetes 7	47	0.052

134		CHR074	Choriocarcinoma	47	0.052

135		EXS001	Exostosis	46	0.052

136		MDD018	Middle East Respiratory Syndrome	43	0.052

137	c	PSR028	Psoriasis 7	42	0.052

138		OCL052	Ocular Dominance	42	0.052

139	c	CFF007	Coffin-Siris Syndrome 2	41	0.052

140	c	MCR130	Microvascular Complications of Diabetes 6	41	0.052

141	c	MCR133	Microvascular Complications of Diabetes 4	41	0.052

142	c	PSR018	Psoriasis 13	41	0.052

143		48X005	48,xyyy	39	0.052

144	P	PRS040	Prostate Cancer	97	0.042

145	c	LKM061	Leukemia, Acute Myeloid	84	0.042

146		CYS001	Cystic Fibrosis	81	0.042

147	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.042

148	P	HRT032	Heart Disease	75	0.042

149	c	MCP050	Mucopolysaccharidosis, Type Ii	72	0.042

150		DWN001	Down Syndrome	70	0.042

151	P	OST001	Osteopetrosis	70	0.042

152	c	CHR684	Chronic Kidney Disease	70	0.042

153		ADL002	Adult Syndrome	70	0.042

154	P	MYP004	Myopathy	70	0.042

155	P	TYS001	Tay-Sachs Disease	69	0.042

156		MST024	Mastocytosis, Cutaneous	69	0.042

157	P	LVR013	Liver Disease	68	0.042

158		SKN019	Skin Melanoma	68	0.042

159	c	INF071	Inflammatory Bowel Disease 1	67	0.042

160		BRK010	Burkitt Lymphoma	67	0.042

161		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.042

162		LWC002	Lowe Oculocerebrorenal Syndrome	65	0.042

163	P	PSD087	Pseudoxanthoma Elasticum	65	0.042

164	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.042

165		CLF027	Cleft Palate, Isolated	64	0.042

166	c	MCP049	Mucopolysaccharidosis, Type Vii	63	0.042

167		LSH001	Leishmaniasis	63	0.042

168		CLT003	Colitis	62	0.042

169	P	PLY014	Polycystic Kidney Disease	62	0.042

170	c	BRN108	Branchiootic Syndrome 1	62	0.042

171	c	MCP047	Mucopolysaccharidosis, Type Iva	61	0.042

172		NRL005	Neurilemmoma	60	0.042

173	P	CTR002	Cataract	60	0.042

174		PLM033	Pulmonary Embolism	59	0.042

175		PRN019	Perinatal Necrotizing Enterocolitis	59	0.042

176	P	MLN069	Melanoma, Uveal	59	0.042

177		GNG013	Gingivitis	59	0.042

178		IRN001	Iron Deficiency Anemia	59	0.042

179	P	DNG005	Dengue Virus	59	0.042

180		ADN018	Adenoma	59	0.042

181		ISC004	Ischemia	58	0.042

182	P	EHL001	Ehlers-Danlos Syndrome	58	0.042

183	c	MCP004	Mucopolysaccharidosis Iv	57	0.042

184	P	UVT001	Uveitis	57	0.042

185	c	LKM070	Leukemia, Acute Monocytic	57	0.042

186	P	BPL003	Bipolar Disorder	56	0.042

187		HMT008	Hematuria, Benign Familial	56	0.042

188		EXF001	Exfoliation Syndrome	56	0.042

189		SFT003	Soft Tissue Sarcoma	56	0.042

190		EMB004	Embryonal Carcinoma	56	0.042

191		INT030	Intracranial Aneurysm	56	0.042

192		AGN016	Aging	56	0.042

193		NPH009	Nephrolithiasis	55	0.042

194	P	ART021	Arteriosclerosis	54	0.042

195	P	EPD016	Epidermolysis Bullosa	53	0.042

196		KRT006	Keratoconjunctivitis	53	0.042

197	P	MNC007	Monocytic Leukemia	53	0.042

198		CRH005	Crohn's Colitis	53	0.042

199	c	PRD040	Periodontitis, Chronic	53	0.042

200		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	53	0.042

201	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.042

202		ACT200	Acute Monoblastic Leukemia	52	0.042

203	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.042

204		ENT011	Enterocolitis	51	0.042

205		SPN019	Spondylolisthesis	51	0.042

206		ENT004	Enthesopathy	49	0.042

207		BLL004	Bullous Keratopathy	49	0.042

208		47X002	47,xyy	49	0.042

209	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.042

210		DRY001	Dry Eye Syndrome	47	0.042

211		KRT008	Keratopathy	47	0.042

212	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.042

213		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.042

214	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.042

215	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.042

216	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.042

217	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.042

218	P	CHR345	Chronic Pain	44	0.042

219	c	PCH010	Pachyonychia Congenita 3	44	0.042

220	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.042

221	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.042

222		MYF002	Myofascial Pain Syndrome	42	0.042

223	c	HYP057	Hypervitaminosis D	42	0.042

224		MLT162	Multiple Joint Dislocations, Short Stature, and Craniofacial Dysmorphism with or Without Congenital Heart Defects	42	0.042

225	P	KLZ004	Kala-Azar 1	41	0.042

226	c	MJR024	Major Affective Disorder 9	41	0.042

227	c	EXS020	Exostoses, Multiple, Type Ii	40	0.042

228		KLD004	Keloid Disorder	40	0.042

229	c	MJR022	Major Affective Disorder 8	38	0.042

230	P	MRQ003	Morquio Syndrome	37	0.042

231		PLC006	Placental Choriocarcinoma	36	0.042

232		SPN331	Spondyloocular Syndrome	36	0.042

233		HRW001	Hair Whorl	36	0.042

234	c	LKM005	Leukemia, T-Cell, Chronic	34	0.042

235	P	DSB002	Desbuquois Dysplasia	32	0.042

236		EXN003	Exencephaly	31	0.042

237	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	28	0.042

238		ARG004	Argyria	27	0.042

239		URN022	Urinary Tract Infections, Recurrent	27	0.042

240		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.042

241	P	LTH050	Lethal Chondrodysplasia	14	0.042

242		MYL069	Myeloma, Multiple	85	0.030

243	P	PNC035	Pancreatic Cancer	84	0.030

244		NRL016	Neural Tube Defects	82	0.030

245	P	GLM040	Glioma Susceptibility 1	81	0.030

246	P	RHM011	Rheumatoid Arthritis	80	0.030

247	P	BLD134	Bladder Cancer	79	0.030

248	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.030

249		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.030

250	P	LNG064	Lung Cancer Susceptibility 3	78	0.030

251	P	PRK057	Parkinson Disease, Late-Onset	78	0.030

252		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.030

253		AST005	Asthma	76	0.030

254	c	ATR087	Atrial Standstill 1	75	0.030

255		END057	Endometrial Cancer	74	0.030

256		SVR004	Severe Combined Immunodeficiency	73	0.030

257	P	CNR004	Cone-Rod Dystrophy 2	73	0.030

258		ANX010	Anxiety	73	0.030

259	c	HPT073	Hepatitis C Virus	72	0.030

260	P	HNT016	Huntington Disease	72	0.030

261		ACR007	Acromegaly	71	0.030

262	P	EPL164	Epilepsy	71	0.030

263	P	HYP061	Hypertrophic Cardiomyopathy	70	0.030

264	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.030

265		WRN001	Werner Syndrome	69	0.030

266	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.030

267	P	SPR120	Supranuclear Palsy, Progressive, 1	68	0.030

268	P	LYM118	Lymphoma	68	0.030

269		ODN023	Odontochondrodysplasia	68	0.030

270	P	SYS005	Systemic Scleroderma	68	0.030

271		SND001	Sandhoff Disease	68	0.030

272	c	BSL007	Basal Cell Carcinoma	68	0.030

273		BRN024	Bronchitis	68	0.030

274		RCK004	Rickets	68	0.030

275		PNC129	Pancreatic Adenocarcinoma	68	0.030

276	P	THR014	Thrombocytopenia	67	0.030

277	P	CRD119	Cardiac Arrest	67	0.030

278	P	HPT021	Hepatitis	67	0.030

279		CRP001	Carpal Tunnel Syndrome	67	0.030

280	P	SKN015	Skin Carcinoma	66	0.030

281		MYX005	Myxoid Liposarcoma	66	0.030

282	P	EPD009	Epidermolysis Bullosa Dystrophica	66	0.030

283		ACH004	Achondroplasia	66	0.030

284		LBR036	Leber Plus Disease	66	0.030

285	c	MSC165	Muscular Dystrophy, Congenital, Lmna-Related	66	0.030

286	P	MNN013	Meningitis	66	0.030

287	P	DRM053	Dermatitis, Atopic	66	0.030

288	P	PLM036	Pulmonary Fibrosis	65	0.030

289		HTC003	Hutchinson-Gilford Progeria Syndrome	65	0.030

290		SRC014	Sarcoma	65	0.030

291	P	LPS002	Liposarcoma	65	0.030

292	P	MTR014	Motor Neuron Disease	65	0.030

293		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.030

294		PRT037	Pertussis	65	0.030

295	P	CHR071	Charcot-Marie-Tooth Disease	65	0.030

296		APN008	Apnea, Obstructive Sleep	64	0.030

297		GT001	Gout	64	0.030

298		MSC007	Muscle Hypertrophy	64	0.030

299		OST017	Osteomyelitis	64	0.030

300	P	RHB003	Rhabdomyosarcoma	63	0.030

301	P	VSC007	Vascular Disease	63	0.030

302	c	MLG084	Malignant Fibrous Histiocytoma	63	0.030

303		INT146	Intervertebral Disc Disease	63	0.030

304	P	END044	Endometriosis	63	0.030

305	c	ATM011	Autoimmune Hepatitis	63	0.030

306		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.030

307		LPD008	Lipid Metabolism Disorder	62	0.030

308	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.030

309	c	HPT003	Hepatitis a	62	0.030

310	c	SVR001	Severe Acute Respiratory Syndrome	62	0.030

311	P	HYP750	Hypertriglyceridemia, Familial	62	0.030

312	P	LRS001	Larsen Syndrome	62	0.030

313		LVR012	Liver Cirrhosis	62	0.030

314		CHL068	Cholestasis	61	0.030

315	P	DRM010	Dermatomyositis	61	0.030

316		FTT001	Fatty Liver Disease	61	0.030

317		DRM006	Dermatitis	61	0.030

318	P	ENC004	Encephalitis	61	0.030

319	P	STS008	Sotos Syndrome 1	61	0.030

320	P	PNC044	Pancreatitis	61	0.030

321	P	SJG008	Sjogren Syndrome	61	0.030

322		RTN017	Retinal Detachment	61	0.030

323		NPH091	Nephrolithiasis, Calcium Oxalate	60	0.030

324	P	SCL018	Scoliosis	60	0.030

325	c	ACT027	Acute Pancreatitis	60	0.030

326		RHM001	Rheumatic Fever	60	0.030

327	P	USH001	Usher Syndrome	60	0.030

328	P	MYC008	Myocarditis	59	0.030

329		CHL014	Cholera	59	0.030

330		IGR001	Ige Responsiveness, Atopic	59	0.030

331	c	DNG003	Dengue Disease	59	0.030

332	P	BRS044	Breast Adenocarcinoma	59	0.030

333		GRD007	Grade Iii Astrocytoma	59	0.030

334	P	GLL022	Guillain-Barre Syndrome	59	0.030

335		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.030

336		ANR040	Aneurysm	59	0.030

337		PSD012	Pseudoachondroplasia	58	0.030

338	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.030

339		ANT024	Anthrax Disease	58	0.030

340		CNT047	Contact Dermatitis	58	0.030

341		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.030

342		BRS051	Breast Disease	58	0.030

343	P	PRP019	Peripheral Nervous System Disease	58	0.030

344		CHR070	Chronic Inflammatory Demyelinating Polyradiculoneuropathy	57	0.030

345	P	EXN002	Exanthem	57	0.030

346	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.030

347		LYM021	Lymphadenitis	57	0.030

348	P	FCL005	Focal Segmental Glomerulosclerosis	57	0.030

349		TNS005	Tonsillitis	57	0.030

350		JPN002	Japanese Encephalitis	57	0.030

351		AYM001	Ayme-Gripp Syndrome	57	0.030

352	P	ANG015	Angioedema	57	0.030

353		BCT022	Bacterial Infectious Disease	56	0.030

354	P	SZR006	Seizure Disorder	56	0.030

355		ALL010	Allergic Contact Dermatitis	56	0.030

356		OVR012	Ovarian Serous Cystadenocarcinoma	56	0.030

357		PYC001	Pycnodysostosis	56	0.030

358	P	GST044	Gastritis	56	0.030

359	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.030

360		HYP005	Hypokalemia	55	0.030

361		FND002	Fundus Dystrophy	55	0.030

362	P	DRR001	Diarrhea	55	0.030

363	P	GRV001	Graves' Disease	55	0.030

364	P	LRY044	Larynx Cancer	55	0.030

365	P	SLM003	Salmonellosis	55	0.030

366		CLF004	Cleft Lip/palate	54	0.030

367		GLS001	Gliosarcoma	54	0.030

368		AMN003	Amnestic Disorder	54	0.030

369		GLC003	Glucose Intolerance	54	0.030

370		MSC162	Muscular Dystrophy, Congenital Merosin-Deficient, 1a	54	0.030

371		MCL075	Macular Dystrophy, Corneal	54	0.030

372		TND005	Tendinitis	54	0.030

373	c	MLG077	Malignant Peripheral Nerve Sheath Tumor	54	0.030

374		DBT010	Diabetic Neuropathy	54	0.030

375		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	54	0.030

376		RCS002	Recessive Dystrophic Epidermolysis Bullosa	54	0.030

377	P	BRC006	Brachydactyly	53	0.030

378	P	END047	Endophthalmitis	53	0.030

379		OST016	Osteochondrosis	53	0.030

380	P	CTN003	Cutaneous Lupus Erythematosus	53	0.030

381		CLF001	Cleft Lip	53	0.030

382		SPN035	Spindle Cell Sarcoma	53	0.030

383	P	ACT008	Actinic Keratosis	53	0.030

384		OVR059	Ovary Adenocarcinoma	53	0.030

385	P	RTN018	Retinal Disease	53	0.030

386		DMY004	Demyelinating Disease	52	0.030

387	c	EPD076	Epidermolysis Bullosa Dystrophica, Autosomal Recessive	52	0.030

388	c	MSC169	Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1	52	0.030

389		LYS002	Lysosomal Storage Disease	52	0.030

390	P	DDN001	Duodenal Ulcer	52	0.030

391	P	CNG436	Congenital Disorder of Deglycosylation	52	0.030

392		ART074	Aortic Dissection	52	0.030

393	P	TRT010	Teratoma	52	0.030

394		PRV004	Periventricular Leukomalacia	52	0.030

395	c	INH030	Inherited Retinal Disorder	51	0.030

396		NPH003	Nephrocalcinosis	51	0.030

397		KRT009	Keratosis	51	0.030

398		MYL001	Myelitis	51	0.030

399		PLS009	Plasma Cell Neoplasm	51	0.030

400	c	PNC106	Pancreatic Agenesis 1	51	0.030

401		VSC006	Vascular Cancer	51	0.030

402		CLB002	Clubfoot	51	0.030

403		NRM004	Neuroma	51	0.030

404		BLL003	Bell's Palsy	51	0.030

405		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.030

406		HYP781	Hypoascorbemia	51	0.030

407		PLR008	Pleurisy	50	0.030

408		ABN011	Abnormal Hair, Joint Laxity, and Developmental Delay	50	0.030

409		BRN009	Burning Mouth Syndrome	50	0.030

410		STM007	Stomatitis	50	0.030

411	P	AGG001	Aggressive Periodontitis	50	0.030

412	P	KRT007	Keratoconus	50	0.030

413		NTR046	Neutrophil Migration	50	0.030

414	P	OTS001	Otosclerosis	49	0.030

415	P	CRN025	Corneal Dystrophy	49	0.030

416		PLY024	Polymicrogyria	49	0.030

417		AMB002	Amblyopia	49	0.030

418	c	ACH042	Achondrogenesis, Type Ib	49	0.030

419		BCT004	Bacteriuria	49	0.030

420		VCC001	Vaccinia	49	0.030

421		LRN003	Learning Disability	49	0.030

422	c	DSB006	Desbuquois Dysplasia 1	48	0.030

423		ATS010	Autosomal Recessive Disease	48	0.030

424		CLS016	Clostridium Difficile Colitis	48	0.030

425		PNC034	Pancreas Disease	48	0.030

426		PYL006	Pyloric Stenosis	48	0.030

427		HLX001	Helix Syndrome	47	0.030

428		PPL002	Papillary Carcinoma	47	0.030

429		RNL077	Renal Fibrosis	47	0.030

430		KRT002	Keratomalacia	47	0.030

431	c	HMN021	Human T-Cell Leukemia Virus Type 1	47	0.030

432		AML029	Ameloblastoma	46	0.030

433		CMP012	Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome	46	0.030

434		SPN411	Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related	46	0.030

435		KRT013	Keratolytic Winter Erythema	46	0.030

436		TXC011	Toxocariasis	46	0.030

437		SCL002	Scleredema Adultorum	46	0.030

438	P	HRD001	Hereditary Multiple Exostoses	46	0.030

439		SVN002	Sveinsson Chorioretinal Atrophy	46	0.030

440		MYX013	Myxofibrosarcoma	45	0.030

441	c	GM2006	Gm2 Gangliosidosis	45	0.030

442	c	ATM099	Autoimmune Uveitis	45	0.030

443		LRY022	Laryngoonychocutaneous Syndrome	44	0.030

444		CYS009	Cystadenoma	44	0.030

445		FCH001	Fuchs' Endothelial Dystrophy	44	0.030

446		SCH030	Schneckenbecken Dysplasia	44	0.030

447	P	GNG009	Gangliosidosis	44	0.030

448	P	FBR003	Fibrous Histiocytoma	44	0.030

449		DYS018	Dysostosis	44	0.030

450		FBR054	Fibroma	44	0.030

451		CHN010	Chondroma	43	0.030

452		SPN369	Spinal Disease	43	0.030

453		TND004	Tendinopathy	43	0.030

454		RFR003	Refractive Error	43	0.030

455		DYS032	Dystrophinopathies	43	0.030

456	P	CRN026	Corneal Edema	43	0.030

457	P	DMY001	Demyelinating Polyneuropathy	43	0.030

458		BCL002	B Cell Deficiency	43	0.030

459		PRS036	Parasitic Protozoa Infectious Disease	43	0.030

460		DSC009	Discoid Lupus Erythematosus	42	0.030

461		SNL007	Senile Cataract	42	0.030

462	c	CNG023	Congenital Fibrosarcoma	42	0.030

463		ATX019	Ataxia with Vitamin E Deficiency	42	0.030

464		CTS005	Catastrophic Antiphospholipid Syndrome	42	0.030

465	c	MLG079	Malignant Pleural Mesothelioma	42	0.030

466		IDP070	Idiopathic Scoliosis	42	0.030

467		TND006	Tendinosis	42	0.030

468		EPC002	Epicondylitis	41	0.030

469		MNN002	Mononeuritis Multiplex	41	0.030

470		LCH016	Lichen Sclerosus Et Atrophicus	41	0.030

471		XRP001	Xerophthalmia	41	0.030

472		PLY183	Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome	41	0.030

473		SPN362	Spondylometaphyseal Dysplasia, Sedaghatian Type	41	0.030

474	P	HYP009	Hypertrophic Pyloric Stenosis	41	0.030

475		VSL013	Visual Impairment and Progressive Phthisis Bulbi	41	0.030

476	c	HYP072	Hypersensitivity Reaction Type Iii Disease	40	0.030

477		BRS050	Breast Cyst	40	0.030

478	P	MSC134	Musculocontractural Ehlers-Danlos Syndrome	40	0.030

479		WLL004	Wallerian Degeneration	39	0.030

480		SPP007	Suppression Amblyopia	39	0.030

481	P	BRC003	Brachyolmia	39	0.030

482	c	HRD104	Hereditary Multiple Osteochondromas	39	0.030

483		AML001	Amelanotic Melanoma	39	0.030

484		CRN288	Corneal Dystrophy, Band-Shaped	38	0.030

485		OVR094	Ovarian Epithelial Cancer	38	0.030

486		HPT070	Hepatosplenic T-Cell Lymphoma	38	0.030

487		DYS006	Dysembryoplastic Neuroepithelial Tumor	38	0.030

488		SHW001	Shwartzman Phenomenon	37	0.030

489		OPS002	Opsismodysplasia	37	0.030

490		DDN027	Duodenum Disease	37	0.030

491		GLM044	Glomerular Disease	37	0.030

492		WGN003	Wagner Syndrome	36	0.030

493	P	AXN001	Axonal Neuropathy	36	0.030

494	P	LMN012	Laminin Subunit Alpha 2-Related Congenital Muscular Dystrophy	35	0.030

495		PNC005	Penicilliosis	34	0.030

496		HMP018	Hemophilic Arthropathy	34	0.030

497	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.030

498	c	PYL018	Pyloric Stenosis, Infantile Hypertrophic, 1	33	0.030

499		PPL052	Papillomatosis, Confluent and Reticulated	33	0.030

500	c	SBC035	Subacute Cutaneous Lupus Erythematosus	32	0.030

501		SCL025	Scleromyxedema	32	0.030

502		ENC014	Enchondroma	29	0.030

503	c	LM2001	Lama2-Related Muscular Dystrophy	26	0.030

504	P	QLT011	Qualitative or Quantitative Defects of Sarcoglycan	26	0.030

505		MLG164	Malignant Epithelial Tumor of Ovary	26	0.030

506		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.030

507		PRN071	Parenteral Nutrition-Associated Cholestasis	25	0.030

508		OVR098	Ovarian Fibroma	25	0.030

509		MCN011	Mucinoses	24	0.030

510		DRM046	Dermal Ridges-off-the-End	24	0.030

511		CRN023	Corneal Deposit	22	0.030

512		CRT057	Critical Congenital Heart Disease	21	0.030

513		GLS013	Glossodynia	18	0.030

514		BRC114	Brachyolmia Type 1, Hobaek Type	17	0.030

515		CLF034	Cleft Hard Palate	16	0.030

516		SKL033	Skeletal Dysplasia, Mild, with Joint Laxity and Advanced Bone Age	12	0.030

517		MCP042	Mucopolysaccharidoses, Unclassified Types	10	0.030