Search results for "lymphoproliferative syndrome"

The MalaCard for "lymphoproliferative syndrome" has been retired.
Searching MalaCards for entries containing "lymphoproliferative syndrome"

634 hits were found for 'lymphoproliferative syndrome'

#	Family	MCID	Name	MIFTS	Score
1	c	ATM006	Autoimmune Lymphoproliferative Syndrome	71	7.767

2	P	LYM113	Lymphoproliferative Syndrome, X-Linked, 1	51	7.105

3	c	ATM030	Autoimmune Lymphoproliferative Syndrome, Type Ii	32	4.714

4	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	30	4.694

5		RSS025	Ras-Associated Autoimmune Leukoproliferative Disorder	41	4.691

6	c	LYM114	Lymphoproliferative Syndrome, X-Linked, 2	43	4.688

7	P	LYM033	Lymphoproliferative Syndrome	56	4.376

8	c	ATM046	Autoimmune Lymphoproliferative Syndrome, Type Iib	37	4.295

9	c	LYM107	Lymphoproliferative Syndrome 2	50	4.126

10	c	ATM083	Autoimmune Lymphoproliferative Syndrome, Type Iii	38	4.045

11	c	LYM106	Lymphoproliferative Syndrome 1	32	3.859

12		DNZ002	Dianzani Autoimmune Lymphoproliferative Disease	10	3.646

13	c	ATM087	Autoimmune Lymphoproliferative Syndrome Due to Ctla4 Haploinsuffiency	10	3.238

14	c	PRK077	Prkcd-Related Autoimmune Lymphoproliferative Syndrome	12	2.478

15	c	ATS229	Autosomal Recessive Lymphoproliferative Disease	19	1.976

16		IGG007	Igg4-Related Disease	38	1.549

17		LYM054	Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1	4	1.453

18	c	ATM027	Autoimmune Lymphoproliferative Syndrome, Type 0	11	1.441

19	c	CSP002	Casp10-Related Autoimmune Lymphoproliferative Syndrome	7	1.440

20	c	FSL002	Faslg-Related Autoimmune Lymphoproliferative Syndrome	7	1.440

21	c	FSR002	Fas-Related Autoimmune Lymphoproliferative Syndrome	7	1.440

22	P	LYM118	Lymphoma	69	0.323

23		PST046	Post-Transplant Lymphoproliferative Disease	54	0.287

24	P	LKM002	Leukemia	71	0.240

25		ADL002	Adult Syndrome	52	0.182

26		LYM024	Lymphatic System Disease	52	0.175

27	c	HYP073	Hypersensitivity Reaction Type Iv Disease	43	0.172

28	P	HPT021	Hepatitis	69	0.160

29		LYM023	Lymphatic System Cancer	33	0.152

30		KDS001	Kid Syndrome	53	0.151

31		CHL071	Child Syndrome	58	0.150

32		MYL009	Myelodysplastic Syndrome	73	0.144

33	P	BCL006	B-Cell Lymphomas	65	0.144

34		IMM136	Immune System Disease	51	0.140

35		C3D001	C3 Deficiency	53	0.137

36		LYM019	Lymphosarcoma	53	0.135

37	c	CHR090	Chronic Lymphocytic Leukemia	76	0.132

38		HDG012	Hodgkin Lymphoma	77	0.129

39		CRB009	Cerebritis	39	0.129

40	c	ADL001	Adult Lymphoma	39	0.128

41		ALR002	Al-Raqad Syndrome	36	0.128

42	P	ART022	Arthritis	75	0.128

43	P	LYM026	Lymphoblastic Leukemia	62	0.124

44		INC022	Inclusion-Cell Disease	46	0.120

45		WLL006	Wells Syndrome	59	0.120

46		HMT018	Hematopoietic Stem Cell Transplantation	41	0.119

47		AND005	Androgen Insensitivity Syndrome, Mild	16	0.119

48	P	THR014	Thrombocytopenia	64	0.116

49	P	HMP002	Hemophagocytic Lymphohistiocytosis	64	0.116

50		LYM067	Lymphoid Leukemia	44	0.115

51	c	CHR418	Chronic Leukemia	47	0.114

52	P	AXN010	Axenfeld-Rieger Syndrome, Type 3	55	0.112

53		GDS001	Good Syndrome	44	0.112

54		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	48	0.109

55	P	RHM011	Rheumatoid Arthritis	89	0.108

56		LYM051	Lymphomatoid Granulomatosis	47	0.107

57		HPT074	Hepatic Adenoma, Somatic	50	0.107

58		LYM115	Lymphoma, Non-Hodgkin	63	0.107

59	P	WSK001	Wiskott-Aldrich Syndrome	73	0.106

60		VSC011	Vasculitis	62	0.106

61		HNM002	Hinman Syndrome	25	0.106

62		MYC006	Mycosis Fungoides	66	0.105

63	c	ACT073	Acute Leukemia	60	0.103

64		PLS011	Plasmacytoma	56	0.103

65	P	ANP001	Anaplastic Large Cell Lymphoma	57	0.103

66		TNP003	Tn Polyagglutination Syndrome, Somatic	41	0.101

67		CMM004	Common Variable Immunodeficiency	68	0.101

68	P	EPL164	Epilepsy	66	0.100

69	c	LKM004	Leukemia, B-Cell, Chronic	24	0.099

70		CSY001	C Syndrome	50	0.099

71	P	LPS004	Lupus Erythematosus	64	0.099

72		BLD054	Blood Protein Disease	37	0.098

73		SPL018	Splenomegaly	44	0.098

74		VRL011	Viral Infectious Disease	55	0.098

75	P	HYP098	Hypereosinophilic Syndrome	63	0.097

76	P	FTL001	Fetal Alcohol Syndrome	53	0.097

77	c	SYS001	Systemic Lupus Erythematosus	86	0.096

78		DFF005	Diffuse Large B-Cell Lymphoma	59	0.095

79		MRG013	Mirage Syndrome	29	0.095

80	P	PNM007	Pneumonia	68	0.095

81	c	LKM050	Leukemia, Chronic Lymphocytic 1	19	0.095

82	P	TCL004	T-Cell Leukemia	47	0.094

83	P	APL001	Aplastic Anemia	75	0.094

84	P	ENC018	Encephalopathy	59	0.094

85		DRG012	Drug Rash with Eosinophilia and Systemic Symptoms	35	0.093

86	c	PRM023	Pre-Malignant Neoplasm	41	0.093

87		LKC003	Leukocyte Disease	43	0.092

88		LYM052	Lymphomatoid Papulosis	41	0.092

89	P	HYP071	Hypersensitivity Reaction Type Ii Disease	49	0.092

90		THR024	Thrombosis	57	0.091

91		THR013	Thoracic Outlet Syndrome	50	0.091

92	P	MYL006	Myeloid Leukemia	66	0.090

93	P	PNC044	Pancreatitis	61	0.089

94		PRP030	Purpura	58	0.089

95	P	BLD051	Blood Coagulation Disease	42	0.089

96		SPL012	Splenic Disease	46	0.088

97	c	ADL017	Adult T-Cell Leukemia	60	0.088

98		VSC008	Vascular Hemostatic Disease	30	0.088

99		PRP036	Peripheral T-Cell Lymphoma	45	0.088

100		BNM001	Bone Marrow Cancer	51	0.088

101	P	HMR003	Hemorrhagic Disease	57	0.087

102		BLD053	Blood Platelet Disease	46	0.086

103		SRC014	Sarcoma	66	0.086

104	P	MLT019	Multiple Myeloma	83	0.086

105	P	HML002	Hemolytic Anemia	62	0.086

106		CRD118	Cardiovascular Cancer	44	0.086

107		MTH049	Methotrexate-Associated Lymphoproliferative Disorders	17	0.086

108		END072	Endotheliitis	42	0.085

109		VSC006	Vascular Cancer	51	0.085

110	c	HPT001	Hepatitis C	68	0.085

111	P	GLM007	Glomerulonephritis	59	0.085

112		MCR004	Macroglobulinemia	50	0.084

113		MNT001	Mantle Cell Lymphoma	72	0.084

114		ACD009	Acid-Labile Subunit, Deficiency of	45	0.084

115		HMT002	Hematologic Cancer	64	0.084

116	c	LKM056	Leukemia, Chronic Lymphocytic 2	21	0.083

117		HRY003	Hairy Cell Leukemia	57	0.083

118	P	HYP055	Hypoplastic Left Heart Syndrome	61	0.082

119		CRY004	Cryoglobulinemia	46	0.082

120		ANG046	Angioimmunoblastic T-Cell Lymphoma	43	0.081

121		SZR001	Sezary's Disease	52	0.081

122	P	NRP001	Neuropathy	59	0.081

123		PLS009	Plasma Cell Neoplasm	48	0.080

124		BRT030	Birth Defects	43	0.080

125		CHR276	Chronic Active Epstein-Barr Virus Infection	44	0.080

126	c	ABD014	Abdominal Obesity-Metabolic Syndrome 1	52	0.079

127		PRM243	Primary Bone Cancer	29	0.078

128		ACT118	Acute Non Lymphoblastic Leukemia	30	0.078

129	c	ATM011	Autoimmune Hepatitis	60	0.077

130		ACR041	Acromelic Frontonasal Dysostosis	45	0.077

131		RTC005	Reticulosarcoma	48	0.076

132	P	CRV039	Cervicitis	45	0.076

133	c	ATM010	Autoimmune Hemolytic Anemia	61	0.076

134	P	HPT023	Hepatocellular Carcinoma	92	0.076

135	P	INT068	Intestinal Disease	60	0.076

136		MRG003	Marginal Zone B-Cell Lymphoma	52	0.076

137	P	SCK002	Sick Sinus Syndrome	50	0.075

138		SPL011	Spleen Cancer	36	0.075

139	P	SJG001	Sjogren's Syndrome	50	0.075

140		RFR004	Refractory Hematologic Cancer	28	0.074

141		PRR002	Pure Red-Cell Aplasia	47	0.074

142	P	FLL037	Follicular Lymphoma	70	0.074

143		SVR004	Severe Combined Immunodeficiency	69	0.074

144	P	PFF001	Pfeiffer Syndrome	73	0.074

145		LYM040	Lymphoblastic Lymphoma	53	0.074

146		SKN016	Skin Disease	66	0.074

147	P	AMY004	Amyloidosis	65	0.074

148	P	NTR004	Neutropenia	59	0.074

149		LRN003	Learning Disability	49	0.074

150		MTH009	Mouth Disease	61	0.073

151		ALL026	Allergic Hypersensitivity Disease	52	0.073

152		DFC004	Deficiency Anemia	64	0.073

153	P	DGR001	Digeorge Syndrome	53	0.073

154		RTC009	Reticulum Cell Sarcoma	47	0.073

155	P	ENC004	Encephalitis	63	0.072

156		PLS025	Plasmablastic Lymphoma	46	0.072

157	c	LKM051	Leukemia, Chronic Lymphocytic 3	19	0.072

158		FML039	Female Reproductive System Disease	48	0.072

159		ATM012	Autoimmune Disease of Blood	35	0.072

160	P	UVT001	Uveitis	58	0.072

161		PRM155	Primary Cutaneous Anaplastic Large Cell Lymphoma	39	0.071

162		ATM052	Autoimmune Disease 1	25	0.071

163		LYM104	Lymphoma, Malt, Somatic	54	0.070

164	c	FLL041	Follicular Lymphoma 1	45	0.070

165		LYM012	Lymphoplasmacytic Lymphoma	44	0.070

166		STF001	Stiff-Person Syndrome	56	0.070

167		PLS016	Plasma Cell Leukemia	42	0.070

168	P	PRC017	Precursor Lymphoblastic Lymphoma/leukemia	32	0.069

169	P	WLD002	Waldenstrom Macroglobulinemia	58	0.069

170		SPL004	Splenic Marginal Zone Lymphoma	44	0.069

171		BCL012	B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue	37	0.069

172		HDG004	Hodgkin's Granuloma	24	0.069

173		CHL061	Childhood Leukemia	49	0.069

174	P	ACT074	Acute Lymphocytic Leukemia	56	0.069

175		HDG006	Hodgkin's Paragranuloma	17	0.069

176		NTR005	Nutritional Deficiency Disease	36	0.069

177		LMB002	Lambert-Eaton Myasthenic Syndrome	49	0.068

178		LYM116	Lymph Node Disease	47	0.068

179	c	HPT073	Hepatitis C Virus	73	0.067

180		ATM053	Autoimmune Disease 2	16	0.067

181		BRK010	Burkitt Lymphoma	69	0.067

182	P	PNC001	Pancytopenia	52	0.067

183		MLR004	Malaria	83	0.067

184		BNC003	Bone Cancer	58	0.067

185		CLL014	Cll/sll	42	0.066

186		LRG008	Large Granular Lymphocyte Leukemia	39	0.066

187		BNS002	Bone Structure Disease	37	0.066

188		PRM097	Primary Immunodeficiency Disease	60	0.066

189		ACQ017	Acquired Von Willebrand Syndrome	37	0.065

190	P	BRS047	Breast Cancer	100	0.065

191	c	MSC109	Mosaic Variegated Aneuploidy Syndrome 1	34	0.065

192	P	CTN015	Cutaneous T Cell Lymphoma	50	0.065

193		RCH001	Richter's Syndrome	45	0.065

194		CLN019	Colonic Disease	51	0.065

195	P	CNT005	Central Nervous System Lymphoma	53	0.065

196		EVN001	Evans' Syndrome	43	0.065

197		EPS006	Epstein Syndrome	39	0.064

198	c	CHR064	Chronic Monocytic Leukemia	42	0.064

199	P	CHR084	Chromosomal Disease	32	0.064

200	P	MNN013	Meningitis	67	0.064

201	P	LFR001	Li-Fraumeni Syndrome	75	0.064

202		DRM006	Dermatitis	66	0.064

203		CYT008	Cytomegalovirus Infection	52	0.064

204		TCL002	T-Cell Large Granular Lymphocyte Leukemia	42	0.064

205	c	CRN214	Coronary Heart Disease 5	22	0.064

206		PRP027	Peripheral Vascular Disease	69	0.063

207	c	LKM061	Leukemia, Acute Myeloid	73	0.063

208	c	HPT016	Hepatitis B	65	0.063

209		NTR003	Natural Killer Cell Leukemia	47	0.063

210	P	DRV001	Dravet Syndrome	69	0.063

211		NSY001	N Syndrome	36	0.063

212		LYM126	Lymphoma Aids Related	15	0.063

213	P	ATX010	Ataxia Neuropathy Spectrum	30	0.063

214	P	HST010	Histiocytosis	58	0.063

215		ALN001	Aland Island Eye Disease	45	0.063

216		TTR016	Tetra-Amelia Syndrome	36	0.062

217	P	CRN178	Coronary Heart Disease 6	21	0.062

218	P	FNC043	Fanconi Anemia, Complementation Group E	55	0.062

219		PCK002	Pick Disease	68	0.062

220		PHY002	Physical Disorder	43	0.062

221		DDX002	Ddx41-Related Susceptibility to Familial Myeloproliferative/lymphoproliferative Neoplasms	13	0.061

222		RBR001	Roberts Syndrome	60	0.061

223		ATM055	Autoimmune Disease 4	15	0.061

224	P	CLR023	Colorectal Cancer	97	0.061

225		CLT003	Colitis	60	0.061

226	c	LKM005	Leukemia, T-Cell, Chronic	20	0.061

227		OCL009	Ocular Cancer	59	0.061

228	c	LKM062	Leukemia, Acute Lymphoblastic	64	0.061

229	c	CRN173	Coronary Heart Disease 8	18	0.061

230		RPR002	Reproductive System Disease	41	0.061

231		KPS004	Kaposi Sarcoma	67	0.060

232		NDL020	Nodal Marginal Zone B-Cell Lymphoma	35	0.060

233		PLS003	Plasmacytic Leukemia	21	0.060

234	c	ADL052	Adult Acute Lymphocytic Leukemia	44	0.060

235	c	ACT020	Acute T Cell Leukemia	35	0.060

236		GRY002	Gray Platelet Syndrome	55	0.060

237		HRT007	Heart Cancer	46	0.060

238	P	HRT017	Heart Tumor	32	0.060

239	c	ADL079	Adult Heart Tumor	16	0.059

240		BNL002	Bone Lymphoma	32	0.059

241	P	PLY019	Polyneuropathy	56	0.059

242		ATM054	Autoimmune Disease 3	15	0.058

243		INT051	Intussusception	50	0.058

244	P	KDN018	Kidney Disease	66	0.058

245	P	LVR013	Liver Disease	75	0.058

246		MDS022	Mediastinitis	41	0.058

247	P	MYL005	Myelofibrosis	67	0.057

248	P	NJM001	Nijmegen Breakage Syndrome	67	0.057

249		PNN001	Panniculitis	51	0.057

250		HDC001	Headache	54	0.057

251	P	KDN017	Kidney Cancer	65	0.057

252		ATM059	Autoimmune Disease 6	22	0.057

253		INT253	Intestinal Benign Neoplasm	47	0.056

254		SXL003	Sexual Disorder	42	0.056

255	P	PLY017	Polyarteritis Nodosa	51	0.056

256	P	ANG015	Angioedema	52	0.056

257		PRL017	Prolymphocytic Leukemia	47	0.056

258	P	ESP024	Esophagitis	61	0.056

259	P	GRN010	Granular Cell Tumor	47	0.056

260	P	AST007	Astrocytoma	65	0.056

261	c	CRN172	Coronary Heart Disease 3	19	0.055

262	c	HMN021	Human T-Cell Leukemia Virus Type 1	52	0.055

263	c	MCR161	Macroglobulinemia, Waldenstrom 1	27	0.055

264	c	CRN175	Coronary Heart Disease 4	19	0.055

265		ADJ001	Adjustment Disorder	38	0.055

266		ADP007	Adie Pupil	34	0.055

267		APH001	Aphthous Stomatitis	62	0.055

268		GNG013	Gingivitis	61	0.055

269	c	PRM226	Primary Central Nervous System Lymphoma	49	0.054

270		PRP019	Peripheral Nervous System Disease	55	0.054

271	P	NRM001	Neuromyelitis Optica	60	0.054

272	P	FND001	Fundus Albipunctatus	55	0.054

273		HYP063	Hypersplenism	48	0.054

274		TBR010	Tuberculosis	70	0.054

275	P	AGM001	Agammaglobulinemia	64	0.054

276		GRW007	Growth Hormone Deficiency	50	0.053

277		BND014	Bone Development Disease	40	0.053

278		LYM127	Lymphatic Malformations	39	0.053

279		MYL031	Myeloproliferative Neoplasm	58	0.053

280		MLN008	Melanoma	62	0.052

281		STM007	Stomatitis	50	0.052

282		ATN002	Autonomic Nervous System Disease	48	0.052

283		LYM045	Lymphocytic Vasculitis	33	0.052

284	c	ATM024	Autoimmune Pancreatitis	47	0.052

285	c	FML303	Familial/multiple Cancer	14	0.052

286		PRM151	Primary Bone Lymphoma	26	0.052

287		MSL001	Measles	61	0.052

288		ACR002	Acrocapitofemoral Dysplasia	33	0.052

289	P	LKM068	Leukemia, Chronic Myeloid, Somatic	68	0.051

290	P	CLC005	Celiac Disease	68	0.051

291		SPC003	Specific Developmental Disorder	38	0.051

292		HDG009	Hodgkin Lymphoma, Childhood	14	0.051

293		WLK001	Walker-Warburg Syndrome	52	0.051

294		OST017	Osteomyelitis	61	0.051

295		MNC004	Monoclonal Paraproteinemia	34	0.051

296		RFR010	Refractory Anemia	45	0.051

297		TNS005	Tonsillitis	57	0.051

298	P	TRC086	Trichohepatoenteric Syndrome 1	48	0.051

299	c	RNL016	Renal Infectious Disease	20	0.051

300		ABL002	Ablepharon-Macrostomia Syndrome	57	0.051

301		MSC004	Muscle Tissue Disease	34	0.051

302	c	MCR162	Macroglobulinemia, Waldenstrom 2	17	0.051

303	P	PRT013	Portal Hypertension	60	0.051

304	P	FRD001	Friedreich Ataxia	62	0.050

305		HRT029	Heart Tumor of the Child	15	0.050

306		YNG002	Young Syndrome	26	0.050

307		SML025	Small Non-Cleaved Cell Lymphoma	22	0.050

308	P	MSC007	Muscle Hypertrophy	58	0.050

309		MXD023	Mixed Cell Type Cancer	45	0.050

310		IMG001	Image Syndrome	50	0.050

311		ANG025	Angioimmunoblastic Lymphadenopathy with Dysproteinemia	40	0.050

312		STM006	Stomach Disease	50	0.050

313	c	TCL001	T-Cell Adult Acute Lymphocytic Leukemia	24	0.049

314	P	CHR562	Chronic Myelocytic Leukemia	41	0.049

315		CYS001	Cystic Fibrosis	83	0.049

316		SHR102	Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures	43	0.049

317		HMN032	Human Herpesvirus 8	46	0.049

318	P	NRV007	Nervous System Disease	71	0.049

319	P	ASP006	Aspergillosis	61	0.049

320		CRB025	Carbohydrate Metabolic Disorder	46	0.049

321		HYP327	Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy	33	0.049

322		RFR001	Refractory Plasma Cell Neoplasm	16	0.049

323		VND001	Vein Disease	47	0.048

324	P	NRV006	Nervous System Cancer	60	0.048

325		MCS002	Mucositis	55	0.048

326	P	SML016	Small Intestine Cancer	52	0.048

327	c	TCL005	T-Cell Prolymphocytic Leukemia	52	0.048

328		LNR006	Linear Iga Disease	40	0.048

329		TCL019	T-Cell Childhood Lymphoblastic Lymphoma	14	0.048

330	P	TXP001	Toxoplasmosis	61	0.048

331	P	THR005	Thrombotic Thrombocytopenic Purpura	55	0.047

332	c	ACQ012	Acquired Angioedema	39	0.047

333		LYM004	Lymphoid Interstitial Pneumonia	33	0.047

334		ANG049	Angioedema Induced by Ace Inhibitors	34	0.047

335	P	CFF001	Coffin-Siris Syndrome	51	0.047

336		NNH003	Non-Hodgkin Lymphoma, Childhood	12	0.047

337	P	INF037	Inflammatory Bowel Disease	63	0.047

338		BCL010	B-Cell Expansion with Nfkb and T-Cell Anergy	47	0.047

339		PRM026	Primary Systemic Mycosis	37	0.047

340		HPT022	Hepatoblastoma	55	0.047

341	P	XLN007	X-Linked Disease	34	0.046

342		LYM048	Lymphoma, Large-Cell, Immunoblastic	25	0.046

343		SLD003	Sialadenitis	49	0.046

344	P	MYC068	Myoclonic Epilepsy of Infancy	36	0.046

345		ORL011	Oral Cancer	56	0.046

346	P	SKN013	Skin Benign Neoplasm	43	0.046

347		SPN051	Spondylitis	51	0.046

348		ADR038	Adermatoglyphia	46	0.046

349	c	LKM055	Leukemia, Acute Lymphoblastic 2	19	0.046

350	P	SZR006	Seizure Disorder	56	0.046

351		WHT007	White Platelet Syndrome	15	0.045

352	P	MSC005	Muscular Dystrophy	65	0.045

353	c	ACR061	Aicardi-Goutieres Syndrome 1, Dominant and Recessive	43	0.045

354		RSD004	Rosai-Dorfman Disease	41	0.045

355		HST016	Histiocytic Sarcoma	41	0.045

356	c	BCL013	B-Cell Adult Acute Lymphocytic Leukemia	32	0.045

357	P	BLD124	Bleeding Disorder, Platelet-Type, 11	40	0.045

358		CMP001	Composite Lymphoma	37	0.045

359	P	RNL014	Renal Cell Carcinoma	82	0.045

360	P	PRM019	Premature Ovarian Failure	64	0.045

361	P	SPS003	Spastic Diplegia	52	0.045

362		DSS008	Disease of Mental Health	52	0.045

363		RNL007	Renal Tubular Acidosis	50	0.045

364		GST050	Gastrointestinal System Disease	56	0.045

365	c	BNG076	Benign Exophthalmos Syndrome	15	0.045

366	P	LCT001	Lactic Acidosis	51	0.044

367		PRP021	Peripheral Nervous System Neoplasm	46	0.044

368	P	HRP006	Herpes Simplex	65	0.044

369		VRS001	Virus Associated Hemophagocytic Syndrome	35	0.044

370		FRB001	Farber Lipogranulomatosis	53	0.044

371	P	MDL005	Medulloblastoma	77	0.044

372		FNC006	Functional Gastric Disease	32	0.043

373		NRT004	Neuritis	52	0.043

374	P	ORL007	Oral Cavity Cancer	59	0.043

375	P	THR015	Thrombophilia	59	0.043

376		SKN023	Skin Tag	44	0.043

377	P	HYP097	Hyperekplexia	54	0.043

378	c	INV001	Invasive Aspergillosis	47	0.043

379	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	42	0.043

380		HYP266	Hypoxia	56	0.043

381		WHM001	Whim Syndrome	53	0.043

382		LYM020	Lymph Node Cancer	39	0.043

383		BND002	B- and T-Cell Mixed Leukemia	17	0.043

384		ACT103	Acute Lymphoblastic Leukemia, Childhood	41	0.042

385	P	MYS005	Myositis	57	0.042

386		LYM049	Lymphoma, Small Cleaved-Cell, Diffuse	29	0.042

387		LVR006	Liver Lymphoma	27	0.042

388		LYM041	Lymphocytes Absent	13	0.042

389	P	EXN002	Exanthem	57	0.042

390	P	HYP345	Hyper-Ige Recurrent Infection Syndrome	54	0.042

391		SFT003	Soft Tissue Sarcoma	57	0.042

392		ANG037	Angiomatosis	37	0.042

393		BCL002	B Cell Deficiency	49	0.042

394		TBR011	Tuberculous Meningitis	47	0.042

395		TCL003	T Cell Deficiency	45	0.042

396	P	ACT135	Acute Graft Versus Host Disease	53	0.042

397		IPX001	Ipex Syndrome	45	0.042

398		CCN007	Cocoon Syndrome	45	0.042

399		LMY003	Leiomyomatosis	42	0.042

400	P	DMY001	Demyelinating Polyneuropathy	43	0.041

401	P	ATX030	Ataxia-Telangiectasia	77	0.041

402	P	BCL005	B Cell Prolymphocytic Leukemia	43	0.041

403		BLS007	Blastic Plasmacytoid Dendritic Cell	41	0.041

404		INC021	Incontinentia Pigmenti	59	0.041

405	P	PLY018	Polycythemia	58	0.041

406	c	SRC023	Sarcoidosis 2	33	0.041

407		GST078	Gastrointestinal Allergy	40	0.041

408		HPT070	Hepatosplenic T-Cell Lymphoma	39	0.041

409		RFR002	Refractory Hairy Cell Leukemia	29	0.041

410	c	ALM001	Al Amyloidosis	49	0.041

411	P	SNS014	Sinusitis	60	0.041

412	c	TRC078	Trichohepatoenteric Syndrome 2	29	0.041

413	P	PLY041	Polymyositis	52	0.040

414		UND005	Undifferentiated Pleomorphic Sarcoma	44	0.040

415		ADT003	Auditory System Disease	40	0.040

416	P	LDD002	Liddle Syndrome	53	0.040

417		PLC008	Placenta Disease	33	0.040

418	c	ANP011	Anaplastic Small Cell Lymphoma	14	0.040

419	P	KBK002	Kabuki Syndrome 1	49	0.040

420	P	MNC007	Monocytic Leukemia	55	0.040

421		FDL002	Food Allergy	53	0.040

422	c	CNT035	Central Nervous System Disease	60	0.039

423	c	HMN022	Human T-Cell Leukemia Virus Type 2	44	0.039

424		LYM005	Lymphocele	35	0.039

425		GRF001	Graft-Versus-Host Disease, Protection Against	52	0.039

426		NTR018	Neutrophilia, Hereditary	42	0.039

427	P	DRM010	Dermatomyositis	62	0.039

428		HMN014	Human Immunodeficiency Virus Infectious Disease	50	0.039

429		CLD007	Cold Agglutinin Disease	44	0.039

430	P	LPR003	Leprosy	69	0.039

431	P	DYS007	Dyskeratosis Congenita	63	0.038

432		PRG009	Progressive Multifocal Leukoencephalopathy	52	0.038

433		TMR010	Tumor Predisposition Syndrome	47	0.038

434		INT067	Interstitial Nephritis	46	0.038

435		SPN060	Spondylocarpotarsal Synostosis Syndrome	34	0.038

436		VSC009	Vascular Skin Disease	19	0.038

437		EXT010	Extramedullary Plasmacytoma	49	0.038

438		BRN022	Bronchiectasis	50	0.038

439		MLT001	Multiple Chemical Sensitivity	43	0.038

440	c	FNC027	Fanconi Anemia, Complementation Group a	71	0.038

441		ECT004	Ecthyma	35	0.038

442	P	ARC016	Auriculocondylar Syndrome 1	40	0.038

443	P	GST044	Gastritis	56	0.037

444		CRB001	Cerebral Lymphoma	33	0.037

445		ATN003	Autonomic Nervous System Neoplasm	40	0.037

446	P	MST009	Mastocytosis	56	0.037

447	P	LMY004	Leiomyosarcoma	55	0.037

448		LCH009	Lichen Sclerosus	41	0.037

449		LSH001	Leishmaniasis	66	0.037

450	c	LKM060	Leukemia, Acute Lymphoblastic 3	50	0.037

451		MMB001	Membranoproliferative Glomerulonephritis	46	0.037

452		GRN017	Granulocytopenia	44	0.037

453		PLM001	Pulmonary Tuberculosis	67	0.036

454		C1N001	C1 Inhibitor Deficiency	38	0.036

455	c	ACT134	Acute Liver Failure	50	0.036

456	c	HYP539	Hyperekplexia, Hereditary 1, Autosomal Dominant or Recessive	33	0.036

457	P	MCR129	Microvascular Complications of Diabetes 1	54	0.036

458		OPT009	Optic Neuritis	50	0.036

459		HML018	Homologous Wasting Disease	13	0.036

460		OLG003	Oligohydramnios	53	0.036

461		MLY001	Molybdenum Cofactor Deficiency	38	0.036

462		PTY004	Pityriasis Lichenoides	23	0.036

463	c	CLL013	Cell Type Cancer	46	0.035

464		ANG020	Angiosarcoma	53	0.035

465		APP015	Apparent Mineralocorticoid Excess	51	0.035

466		CRY005	Cryptococcosis	50	0.035

467		ATN004	Autonomic Neuropathy	45	0.035

468		ADR007	Adrenoleukodystrophy	72	0.035

469		TST021	Testicular Germ Cell Tumor	69	0.035

470	P	DMN001	Diamond-Blackfan Anemia	69	0.035

471		VSC003	Visceral Leishmaniasis	56	0.035

472		CD4003	Cd40 Ligand Deficiency	46	0.035

473	c	PRM225	Primary Thrombocytopenia	39	0.035

474		ARC008	Auriculo-Condylar Syndrome	30	0.035

475	c	ATM007	Autoimmune Disease of Central Nervous System	25	0.035

476		NSP002	Nasopharyngitis	40	0.035

477	c	CHR096	Chronic Pulmonary Heart Disease	40	0.035

478		CPL005	Capillary Disease	36	0.035

479		ACR005	Acrodermatitis	36	0.035

480		LTH001	Lethal Midline Granuloma	37	0.035

481		ANP010	Anaplastic Plasmacytoma	19	0.035

482		MGR028	Migraine with or Without Aura 1	47	0.034

483	c	HYP072	Hypersensitivity Reaction Type Iii Disease	38	0.034

484	c	THR037	Thrombocytopenia 2	35	0.034

485		MNT045	Montefiore Syndrome	10	0.034

486	P	GLY010	Glycine Encephalopathy	53	0.034

487	c	TYP024	Type Ii Mixed Cryoglobulinemia	33	0.034

488		PRM128	Primary Cutaneous Follicle Center Lymphoma	26	0.034

489		AGN012	Agnathia-Otocephaly Complex	53	0.034

490		GLC077	Glucocorticoid Therapy, Response to	16	0.034

491	P	ESS003	Essential Thrombocythemia	70	0.034

492	c	SYS004	Systemic Mastocytosis	60	0.034

493	c	BRT034	Bartter Syndrome, Type 2	46	0.034

494		XLN215	X-Linked Congenital Generalized Hypertrichosis	16	0.034

495		MRK001	Merkel Cell Carcinoma	52	0.034

496		FLL008	Folliculitis	46	0.034

497	c	CHR531	Charcot-Marie-Tooth Disease, Type 2d	36	0.033

498		PRM129	Primary Cutaneous Marginal Zone B-Cell Lymphoma	35	0.033

499		PLY039	Polymorphic Reticulosis	19	0.033

500		GLC037	Glucocorticoid Resistance	62	0.033

501		TST014	Testicular Cancer	53	0.033

502		PLM017	Pulmonary Alveolar Microlithiasis	46	0.033

503	P	HRD004	Hereditary Breast Ovarian Cancer	57	0.033

504		CRH005	Crohn's Colitis	52	0.033

505		LPR001	Lepromatous Leprosy	50	0.033

506		PRT094	Protoporphyria, Erythropoietic, X-Linked	28	0.033

507		IND005	Indolent B Cell Lymphoma	23	0.033

508		THR100	Thrombocytopenic Purpura, Autoimmune	54	0.033

509	P	CNN004	Connective Tissue Cancer	40	0.033

510	P	PSD003	Pseudohypoaldosteronism	44	0.032

511	P	CRN108	Cranioectodermal Dysplasia 1	48	0.032

512		HST009	Histiocytoma	47	0.032

513		ASP007	Aspiration Pneumonia	47	0.032

514		ANR004	Anuria	45	0.032

515		INT071	Intestinal Perforation	42	0.032

516		SML008	Small Intestine Lymphoma	40	0.032

517		DSS022	Disseminated Peritoneal Leiomyomatosis	17	0.032

518	c	HMN023	Human T-Cell Leukemia Virus Type 3	14	0.032

519		VGT001	Vogt-Koyanagi-Harada Disease	55	0.032

520		FML037	Female Breast Cancer	50	0.032

521		OST085	Osteosarcoma, Somatic	63	0.031

522		CCC002	Coccidiosis	51	0.031

523		CLN015	Colon Adenocarcinoma	50	0.031

524		GNG011	Gingival Disease	46	0.031

525		BNM005	Bone Marrow Necrosis	32	0.031

526		GRD001	Giardiasis	40	0.031

527		INT277	Intellectual Disability-Developmental Delay-Contractures Syndrome	21	0.031

528		MSC077	Muscle Eye Brain Disease	57	0.031

529		UTR033	Uterine Corpus Cancer	49	0.031

530		INF058	Inflammatory Myofibroblastic Tumor	47	0.031

531	c	ART120	Arthrogryposis, Distal, Type 3	42	0.031

532	c	FML108	Familial Breast Cancer	57	0.030

533		CRT002	Cartilage-Hair Hypoplasia	57	0.030

534		CRP002	Croup	37	0.030

535	c	CNN010	Connective Tissue Benign Neoplasm	32	0.030

536	P	GNR002	Generalized Epilepsy with Febrile Seizures Plus	40	0.030

537		RNL021	Renal Tubular Transport Disease	32	0.030

538	P	KRT005	Keratoacanthoma	46	0.030

539		THY043	Thymic Hyperplasia	32	0.030

540	P	CMR001	Camurati-Engelmann Disease	58	0.030

541	c	PRM038	Primary Agammaglobulinemia	30	0.030

542		IST006	Isotretinoin Syndrome	24	0.029

543		ICH002	Ichthyosis Bullosa of Siemens	45	0.029

544		FXF002	Fox-Fordyce Disease	36	0.029

545		SBC024	Subcutaneous Panniculitis-Like T-Cell Lymphoma	34	0.029

546		RNL101	Renal Cell Carcinoma, Papillary	63	0.029

547	c	MSC047	Muscular Dystrophy-Dystroglycanopathy , Type a, 1	40	0.029

548		CLL021	Collagenous Colitis	39	0.029

549		LNG013	Lung Lymphoma	38	0.029

550		EPD005	Epidural Abscess	33	0.029

551		PLY021	Polyradiculopathy	31	0.029

552		THY025	Thymus Cancer	50	0.028

553	c	SPR009	Sporadic Breast Cancer	47	0.028

554		WRT002	Writing Disorder	27	0.028

555		OVR078	Ovarian Cancer, Somatic	50	0.028

556		ULC007	Ulcerative Stomatitis	44	0.028

557		CMB003	Combined T Cell and B Cell Immunodeficiency	42	0.028

558		LKP003	Leukoplakia	38	0.028

559	c	THR110	Thrombocytopenia 6	20	0.028

560		GNG012	Gingival Overgrowth	52	0.028

561	c	THR044	Thrombotic Thrombocytopenic Purpura, Acquired	42	0.028

562		DYS016	Dysgammaglobulinemia	37	0.028

563		KDN013	Kidney Hypertrophy	31	0.028

564	c	LDD003	Liddle Syndrome, Scnn1b-Related	19	0.028

565	c	LDD004	Liddle Syndrome, Scnn1g-Related	19	0.028

566		TCL018	T-Cell Childhood Acute Lymphocytic Leukemia	18	0.028

567		ALK016	Alk-Negative Anaplastic Large Cell Lymphoma	41	0.027

568		CLR012	Clear Cell Adenofibroma	33	0.027

569		IMM066	Immunodeficiency 9	30	0.027

570		BCL008	B-Cell Childhood Acute Lymphoblastic Leukemia	27	0.027

571		ALD010	Aldosteronism, Glucocorticoid-Remediable	49	0.027

572	c	MSC037	Muscular Dystrophy-Dystroglycanopathy , Type a, 4	48	0.027

573		CRY001	Cryptogenic Organizing Pneumonia	44	0.027

574	c	ATS331	Autosomal Recessive Limb-Girdle Muscular Dystrophy	44	0.027

575		OVR094	Ovarian Epithelial Cancer	43	0.027

576	P	HVY001	Heavy Chain Disease	41	0.027

577		OPS001	Opisthorchiasis	36	0.027

578		HRT003	Heart Lymphoma	30	0.027

579	c	LFR003	Li-Fraumeni Syndrome, Chek2-Related	20	0.027

580		VCC001	Vaccinia	46	0.026

581		IND002	Indolent Systemic Mastocytosis	41	0.026

582		IDP074	Idiopathic Bronchiectasis	36	0.026

583		GST014	Gastrointestinal Lymphoma	31	0.026

584		CBB005	Cobblestone Lissencephaly	27	0.026

585	c	MSC124	Muscular Dystrophy, Congenital	55	0.026

586		CLN005	Colon Lymphoma	35	0.026

587		THY026	Thymus Gland Disease	27	0.026

588		ACR097	Acrodermatitis Chronica Atrophicans	27	0.026

589		PRM133	Primary Pulmonary Lymphoma	23	0.026

590		LYM009	Lymphocytic Choriomeningitis	43	0.025

591		SLT001	Solitary Osseous Plasmacytoma	36	0.025

592		LYM015	Lymphocytic Gastritis	31	0.025

593		IMM070	Immunodeficiency 13	27	0.025

594	c	VRL006	Viral Esophagitis	26	0.025

595		BRC016	Brca1 and Brca2 Hereditary Breast and Ovarian Cancer	24	0.025

596		CRC034	Carcinoma Showing Thymus-Like Differentiation	21	0.025

597		CNG101	Congenital Human Immunodeficiency Virus	19	0.025

598		STT009	Sutton Disease 2	18	0.025

599		UPP009	Upper Limb Hypertrophy	14	0.025

600	c	PSD095	Pseudohypoaldosteronism, Type I	53	0.025

601	c	GMM003	Gamma Heavy Chain Disease	46	0.025

602	c	MSC050	Muscular Dystrophy, Congenital, 1b	37	0.025

603		CRN046	Corneal Fleck Dystrophy	36	0.025

604		HDG003	Hodgkin's Lymphoma, Lymphocytic Depletion	32	0.025

605		ORB009	Orbit Lymphoma	26	0.025

606		NCR009	Necrobiotic Xanthogranuloma	22	0.025

607		PTY006	Pityriasis Lichenoides Et Varioliformis Acuta	21	0.025

608		MXD035	Mixed-Type Autoimmune Hemolytic Anemia	17	0.025

609	c	RNL033	Renal Carcinoma, Familial	12	0.025

610	c	MSC042	Muscular Dystrophy-Dystroglycanopathy , Type B, 6	46	0.024

611	c	MSC035	Muscular Dystrophy-Dystroglycanopathy , Type B, 5	44	0.024

612	c	PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	44	0.024

613	c	PSD096	Pseudohypoaldosteronism Type I, Autosomal Dominant	42	0.024

614	c	MSC103	Muscular Dystrophy-Dystroglycanopathy , Type C, 4	36	0.024

615		CHR068	Chronic Nk-Cell Lymphocytosis	33	0.024

616		CHR076	Choriocarcinoma of the Testis	31	0.024

617		ESN017	Eosinophilic Granuloma	30	0.024

618	P	MSC002	Muscular Dystrophy-Dystroglycanopathy	28	0.024

619		SBC019	Subcutaneous Mycosis	28	0.024

620		PRP013	Paraphimosis	28	0.024

621		IMM038	Immunodeficiency, Common Variable, 1	27	0.024

622		ACQ016	Acquired Pure Red Cell Aplasia	25	0.024

623	c	FKR001	Fkrp-Related Muscle Diseases	23	0.024

624		ANG024	Angiofollicular Lymph Hyperplasia	15	0.024

625	c	MSC059	Muscular Dystrophy, Limb-Girdle, Type 2l	37	0.023

626		ORL019	Oral Hairy Leukoplakia	34	0.023

627	c	GLB007	Glioblastoma 3	31	0.023

628		FLL042	Folliculotropic Mycosis Fungoides	27	0.023

629		EXT048	Extranodal Nasal Nk/t Cell Lymphoma	26	0.023

630		SKN021	Skin Sarcoma	25	0.023

631		INF137	Infections, Recurrent, with Encephalopathy, Hepatic Dysfunction, and Cardiovasuclar Malformations	20	0.023

632		THY006	Thymus Lymphoma	18	0.023

633		CMP062	Complication After Organ Transplantation	11	0.023

634		SML024	Small Intestine Cancer, Childhood	10	0.023