Search results for Adenosine monophosphate

422 hits were found for Adenosine monophosphate

#	Family	MCID	Name	MIFTS	Score
1		ADN029	Adenosine Monophosphate Deaminase 1 Deficiency	34	6.982

2		MYP071	Myopathy Due to Myoadenylate Deaminase Deficiency	27	4.352

3		ERY039	Erythrocyte Amp Deaminase Deficiency	19	3.072

4		ISC004	Ischemia	67	0.248

5		AST005	Asthma	81	0.198

6	P	LKM002	Leukemia	72	0.194

7	P	OVR042	Ovarian Cancer	83	0.189

8		MYL069	Myeloma, Multiple	85	0.186

9		BRR014	Barrett Esophagus	70	0.177

10		HYP266	Hypoxia	63	0.173

11		BRK010	Burkitt Lymphoma	69	0.173

12		RRR001	Rere-Related Disorders	59	0.171

13	P	HPT021	Hepatitis	73	0.154

14		PLM129	Pulmonary Disease, Chronic Obstructive	75	0.147

15	P	MNN013	Meningitis	69	0.141

16	P	ADN016	Adenocarcinoma	70	0.135

17	P	BRS047	Breast Cancer	100	0.131

18	P	RHM011	Rheumatoid Arthritis	81	0.126

19	P	RTN008	Retinitis Pigmentosa	80	0.123

20	P	DBT005	Diabetes Insipidus	55	0.122

21	P	LYM118	Lymphoma	69	0.120

22	P	DBT009	Diabetes Mellitus	67	0.119

23	P	LYM031	Lymphocytic Leukemia	61	0.119

24		CNG034	Congestive Heart Failure	70	0.118

25		WLF001	Wolff-Parkinson-White Syndrome	61	0.118

26	P	MYC007	Myocardial Infarction	78	0.118

27		GLY022	Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency	30	0.117

28		CHR074	Choriocarcinoma	49	0.117

29	P	LVR013	Liver Disease	76	0.116

30	P	PRS040	Prostate Cancer	93	0.116

31	P	ART022	Arthritis	77	0.116

32	P	NRP001	Neuropathy	63	0.115

33		ESP021	Esophageal Cancer	82	0.112

34	c	HYP595	Hypertension, Essential	81	0.112

35	P	PLM037	Pulmonary Hypertension	77	0.112

36	c	PRS136	Prostate Cancer, Hereditary, 6	40	0.109

37	c	PRS130	Prostate Cancer, Hereditary, 8	37	0.109

38		HMT018	Hematopoietic Stem Cell Transplantation	59	0.109

39		SPN012	Spindle Cell Hemangioma	36	0.106

40		INS024	Insulin-Like Growth Factor I	82	0.105

41		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.104

42	P	HML002	Hemolytic Anemia	64	0.102

43		MST004	Mast Cell Neoplasm	42	0.101

44		EXT007	Extracutaneous Mastocytoma	41	0.101

45		CYS001	Cystic Fibrosis	82	0.100

46	c	LKM061	Leukemia, Acute Myeloid	81	0.100

47		ADR054	Adrenocortical Carcinoma, Hereditary	59	0.098

48		ADR016	Adrenal Cortical Carcinoma	57	0.098

49		ADR004	Adrenal Cortical Adenocarcinoma	48	0.098

50	c	SYS001	Systemic Lupus Erythematosus	88	0.097

51	P	LPS004	Lupus Erythematosus	69	0.097

52		NTR027	Neutrophil Actin Dysfunction	32	0.097

53	c	LKM071	Leukemia, Chronic Lymphocytic	78	0.096

54	P	ATR011	Atrial Fibrillation	69	0.096

55	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	92	0.095

56	P	GRF003	Graft-Versus-Host Disease	71	0.094

57	P	CLR023	Colorectal Cancer	99	0.094

58	c	AMY091	Amyotrophic Lateral Sclerosis 1	90	0.094

59	P	MYL006	Myeloid Leukemia	67	0.093

60		INT002	Intermittent Claudication	64	0.093

61	c	ACT210	Acute Respiratory Distress Syndrome	66	0.092

62	P	MSC007	Muscle Hypertrophy	64	0.092

63	c	LKM004	Leukemia, B-Cell, Chronic	38	0.091

64		DPR016	Depression	72	0.091

65	P	LNG032	Lung Cancer	99	0.090

66	c	HPT016	Hepatitis B	70	0.090

67		GST053	Gastric Cancer	78	0.089

68		IMM136	Immune System Disease	57	0.089

69		MLN008	Melanoma	63	0.089

70		DBT010	Diabetic Neuropathy	60	0.088

71	P	HPT023	Hepatocellular Carcinoma	96	0.087

72	P	LYM033	Lymphoproliferative Syndrome	63	0.086

73	P	PSD015	Pseudohypoparathyroidism	51	0.086

74		BNR002	Bone Resorption Disease	54	0.085

75		CHL014	Cholera	60	0.084

76	P	LTR001	Lateral Sclerosis	60	0.084

77		LVR012	Liver Cirrhosis	67	0.083

78	P	HYP073	Hypersensitivity Reaction Type Iv Disease	50	0.082

79		GST033	Gestational Diabetes	63	0.081

80		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	67	0.081

81		THR024	Thrombosis	64	0.080

82		HML018	Homologous Wasting Disease	24	0.079

83	c	MCR113	Microvascular Complications of Diabetes 3	58	0.078

84	c	MCR120	Microvascular Complications of Diabetes 7	46	0.078

85	c	MCR130	Microvascular Complications of Diabetes 6	43	0.078

86	c	MCR133	Microvascular Complications of Diabetes 4	43	0.078

87	P	AST007	Astrocytoma	52	0.078

88		LYM133	Lymphoma, Hodgkin, Classic	72	0.078

89		LYM019	Lymphosarcoma	53	0.078

90		CLT003	Colitis	65	0.078

91	P	GLM045	Glioma	55	0.078

92		GLB002	Glioblastoma	74	0.076

93	P	SCH015	Schizophrenia	73	0.076

94	P	CRD119	Cardiac Arrest	66	0.076

95		MLR004	Malaria	84	0.076

96		THY028	Thyroid Cancer	72	0.076

97		SCK005	Sickle Cell Disease	57	0.076

98		PTT037	Pituitary Tumors	48	0.076

99	c	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.075

100	P	ALZ034	Alzheimer Disease	87	0.074

101	c	ACT074	Acute Lymphocytic Leukemia	63	0.074

102		IMP005	Impotence	56	0.074

103	P	KDN018	Kidney Disease	71	0.073

104		OCL033	Oculocerebral Syndrome with Hypopigmentation	45	0.073

105		RSP006	Respiratory System Disease	64	0.073

106		PRT037	Pertussis	70	0.072

107		ACH004	Achondroplasia	68	0.072

108		IGR001	Ige Responsiveness, Atopic	59	0.072

109		LYM024	Lymphatic System Disease	54	0.072

110		HYP066	Hyperglycemia	64	0.071

111		TRN015	Transient Cerebral Ischemia	59	0.071

112		HPR003	Heparin-Induced Thrombocytopenia	53	0.071

113	P	PNM007	Pneumonia	72	0.070

114		SCK003	Sickle Cell Anemia	74	0.070

115	P	DRM053	Dermatitis, Atopic	71	0.070

116		ALL003	Allergic Rhinitis	70	0.070

117		DRM006	Dermatitis	69	0.070

118	P	MJR001	Major Depressive Disorder	67	0.070

119		OST159	Osteogenic Sarcoma	66	0.070

120	P	RHN004	Rhinitis	64	0.070

121		URM002	Uremia	53	0.070

122		MYL009	Myelodysplastic Syndrome	70	0.069

123	P	LKM062	Leukemia, Acute Lymphoblastic	68	0.069

124		MYL031	Myeloproliferative Neoplasm	64	0.069

125		LYM067	Lymphoid Leukemia	47	0.069

126		BLD054	Blood Protein Disease	43	0.069

127		ACT118	Acute Non Lymphoblastic Leukemia	32	0.069

128	c	ATR087	Atrial Standstill 1	70	0.068

129		ALL026	Allergic Hypersensitivity Disease	68	0.068

130		BRN002	Bronchiolitis	61	0.068

131	P	TRC086	Trichohepatoenteric Syndrome 1	60	0.068

132		BRN012	Bronchiolitis Obliterans	59	0.068

133		THR013	Thoracic Outlet Syndrome	56	0.068

134		ADN018	Adenoma	64	0.066

135	c	CNG027	Congenital Hemolytic Anemia	53	0.066

136		ALL014	Allergic Encephalomyelitis	43	0.066

137		HMN044	Human Immunodeficiency Virus Type 1	75	0.066

138		MVM001	Movement Disease	67	0.066

139		ALL006	Allergic Asthma	61	0.066

140	c	HPT073	Hepatitis C Virus	72	0.064

141		VRL011	Viral Infectious Disease	68	0.064

142		DPH001	Diphtheria	63	0.064

143	P	HMR003	Hemorrhagic Disease	59	0.064

144		LYM040	Lymphoblastic Lymphoma	57	0.064

145	P	HYP024	Hypoparathyroidism	55	0.064

146	P	BLD051	Blood Coagulation Disease	52	0.064

147		VSC008	Vascular Hemostatic Disease	43	0.064

148	P	PHC003	Pheochromocytoma	72	0.064

149	c	LKM056	Leukemia, Chronic Lymphocytic 2	43	0.064

150	c	HPT001	Hepatitis C	69	0.064

151	c	CHR417	Chronic Graft Versus Host Disease	66	0.064

152	c	LKM063	Leukemia, Chronic Myeloid	73	0.063

153		HMG005	Hemoglobinopathy	54	0.063

154	P	FML068	Familial Hypocalciuric Hypercalcemia	50	0.063

155		PMP004	Pemphigus Foliaceus	46	0.063

156		TRT001	Teratocarcinoma	41	0.063

157		SRC014	Sarcoma	70	0.063

158		FTT001	Fatty Liver Disease	66	0.063

159		HYP056	Hypoglycemia	64	0.063

160		LSC001	Lesch-Nyhan Syndrome	62	0.063

161	P	HYP061	Hypertrophic Cardiomyopathy	59	0.063

162		URT010	Ureteral Obstruction	49	0.063

163	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	44	0.063

164	P	MLT020	Multiple Sclerosis	75	0.062

165	c	PLM164	Pulmonary Hypertension, Primary, 1	70	0.062

166	P	MLG056	Malignant Hyperthermia	60	0.062

167		SQM006	Squamous Cell Carcinoma	58	0.062

168	P	TCL004	T-Cell Leukemia	53	0.062

169	P	BLD134	Bladder Cancer	70	0.059

170		ANR007	Anorexia Nervosa	68	0.059

171	P	ANR048	Aniridia 1	64	0.059

172		ACN002	Acanthosis Nigricans	64	0.059

173	P	GRV001	Graves' Disease	61	0.059

174	P	INF037	Inflammatory Bowel Disease	56	0.059

175		RNL077	Renal Fibrosis	51	0.059

176		FSH001	Fish-Eye Disease	50	0.059

177		ATX010	Ataxia Neuropathy Spectrum	39	0.059

178		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	38	0.059

179		PPL052	Papillomatosis, Confluent and Reticulated	33	0.059

180	P	ACT232	Acute Necrotizing Encephalopathy	30	0.059

181		BLD137	Blood Group--Ahonen	24	0.059

182	P	MCR115	Microvascular Complications of Diabetes 5	70	0.059

183	c	SML038	Small Cell Cancer of the Lung	68	0.059

184	P	PRP019	Peripheral Nervous System Disease	66	0.059

185		GLB015	Glioblastoma Multiforme	64	0.059

186		AGN016	Aging	63	0.059

187		HDC001	Headache	62	0.059

188	P	NTR004	Neutropenia	60	0.059

189		BRN080	Brain Ischemia	43	0.059

190	c	ACT135	Acute Graft Versus Host Disease	58	0.058

191	P	PRC017	Precursor Lymphoblastic Lymphoma/leukemia	29	0.058

192	c	VRL010	Viral Hepatitis	60	0.058

193	P	CYS018	Cystitis	58	0.058

194	P	RCT021	Rectum Cancer	58	0.058

195		ATM095	Autoimmune Disease	68	0.056

196	P	ENC018	Encephalopathy	65	0.056

197		HMN014	Human Immunodeficiency Virus Infectious Disease	62	0.056

198	c	BCT007	Bacterial Meningitis	61	0.056

199		STT001	Status Epilepticus	60	0.056

200		GST023	Gastric Ulcer	58	0.056

201		GST071	Gastrointestinal Carcinoma	45	0.056

202		6PH001	6-Phosphogluconate Dehydrogenase Deficiency	29	0.056

203	P	PNC035	Pancreatic Cancer	82	0.056

204	P	INF038	Influenza	75	0.056

205	c	WLM018	Wilms Tumor 5	64	0.056

206		PST028	Post-Traumatic Stress Disorder	63	0.056

207	P	OST001	Osteopetrosis	63	0.056

208	P	GLM007	Glomerulonephritis	61	0.056

209	c	PRM005	Primary Hyperparathyroidism	60	0.056

210	P	HYP069	Hyperparathyroidism	59	0.056

211	P	NNL004	Nonalcoholic Fatty Liver Disease	56	0.056

212		ATN002	Autonomic Nervous System Disease	56	0.056

213		NSD001	Nose Disease	52	0.056

214		RSP021	Respiratory Allergy	48	0.056

215	P	DYS021	Dysautonomia	45	0.056

216		OST012	Osteoarthritis	80	0.053

217		ULC004	Ulcerative Colitis	80	0.053

218	P	NRV007	Nervous System Disease	71	0.053

219		THR100	Thrombocytopenic Purpura, Autoimmune	67	0.053

220		DFC004	Deficiency Anemia	66	0.053

221	P	VSC011	Vasculitis	66	0.053

222		GST049	Gastrointestinal System Cancer	62	0.053

223	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	62	0.053

224	P	BPL003	Bipolar Disorder	61	0.053

225	P	PNS012	Paine Syndrome	60	0.053

226		OVR094	Ovarian Epithelial Cancer	41	0.053

227	P	GLY013	Glycogen Storage Disease	61	0.052

228		MCS002	Mucositis	60	0.052

229		TXC002	Toxic Encephalopathy	57	0.052

230		CPL005	Capillary Disease	45	0.052

231		LYM143	Lymphoma, Non-Hodgkin, Familial	73	0.051

232	c	ATM011	Autoimmune Hepatitis	67	0.051

233		CLF027	Cleft Palate, Isolated	64	0.051

234	c	ACT073	Acute Leukemia	62	0.051

235		CLN015	Colon Adenocarcinoma	57	0.051

236	c	GRV008	Graves Disease 1	57	0.051

237		GTR002	Goiter	54	0.051

238		PRT029	Parathyroid Adenoma	52	0.051

239		HDG002	Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance	49	0.051

240		BSL008	Basal Ganglia Disease	48	0.051

241	c	WLM011	Wilms Tumor 6	40	0.051

242		CRV035	Cervical Cancer	76	0.050

243		MYC006	Mycosis Fungoides	73	0.050

244	P	CHR012	Chronic Granulomatous Disease	69	0.050

245	c	MCR129	Microvascular Complications of Diabetes 1	66	0.050

246	P	ENC004	Encephalitis	66	0.050

247		NRF007	Neurofibroma	66	0.050

248	P	END044	Endometriosis	65	0.050

249		MDD011	Mood Disorder	65	0.050

250	P	PLY014	Polycystic Kidney Disease	62	0.050

251		NRM005	Neuromuscular Disease	61	0.050

252	P	CHN012	Chondrosarcoma	56	0.050

253	P	HYP076	Hyperthyroidism	55	0.050

254		CLR109	Colorectal Adenocarcinoma	54	0.050

255	P	NRB010	Neuroblastoma 1	51	0.050

256		PST053	Postherpetic Neuralgia	45	0.050

257		HPT004	Hepatic Coma	45	0.050

258	c	MCR112	Microvascular Complications of Diabetes 2	42	0.050

259		SQM013	Squamous Cell Carcinoma, Head and Neck	82	0.046

260	P	HRP006	Herpes Simplex	71	0.046

261	P	AGM001	Agammaglobulinemia	71	0.046

262	P	DMN001	Diamond-Blackfan Anemia	70	0.046

263		MYL005	Myelofibrosis	69	0.046

264		PNC033	Pancreas Adenocarcinoma	67	0.046

265		LWC002	Lowe Oculocerebrorenal Syndrome	66	0.046

266		MNT002	Mental Depression	65	0.046

267		PRT058	Pure Autonomic Failure	65	0.046

268		PPT005	Peptic Ulcer Disease	63	0.046

269	P	PNC044	Pancreatitis	62	0.046

270		AND002	Androgen Insensitivity Syndrome	61	0.046

271		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	61	0.046

272	c	ACT027	Acute Pancreatitis	59	0.046

273		DSS009	Disseminated Intravascular Coagulation	58	0.046

274	P	AXN002	Axenfeld-Rieger Syndrome	57	0.046

275		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	55	0.046

276		PRP016	Paraplegia	54	0.046

277		NNL002	Nonalcoholic Steatohepatitis	54	0.046

278	c	DMN023	Diamond-Blackfan Anemia 1	53	0.046

279	P	THY032	Thyroiditis	53	0.046

280	P	RNV001	Renovascular Hypertension	52	0.046

281		KRT002	Keratomalacia	51	0.046

282		HMP009	Haemophilus Influenzae	51	0.046

283		MTB004	Metabolic Acidosis	50	0.046

284		MLG086	Malignant Hyperthermia Susceptibility	41	0.046

285		ALR002	Al-Raqad Syndrome	40	0.046

286	P	NPH012	Nephrotic Syndrome	63	0.045

287		CRY035	Cryptorchidism, Unilateral or Bilateral	61	0.045

288		HDG004	Hodgkin's Granuloma	30	0.045

289		HDG006	Hodgkin's Paragranuloma	22	0.045

290		PFF001	Pfeiffer Syndrome	80	0.042

291		PSY004	Psychotic Disorder	74	0.042

292		ADR007	Adrenoleukodystrophy	71	0.042

293		CNN003	Conn's Syndrome	70	0.042

294	c	WLM013	Wilms Tumor 1	68	0.042

295	P	FLL037	Follicular Lymphoma	67	0.042

296		HSH003	Hashimoto Thyroiditis	67	0.042

297		LGH007	Leigh Syndrome	67	0.042

298		GST040	Gastric Adenocarcinoma	66	0.042

299		LPD008	Lipid Metabolism Disorder	65	0.042

300	P	SNS014	Sinusitis	65	0.042

301		BND020	Bone Disease	64	0.042

302	P	MYP004	Myopathy	64	0.042

303		JNT002	Joint Disorders	64	0.042

304	c	LRG017	Large Intestine Cancer	63	0.042

305		CLN019	Colonic Disease	62	0.042

306	P	INT068	Intestinal Disease	62	0.042

307		PLS011	Plasmacytoma	62	0.042

308		SPN404	Spinal and Bulbar Muscular Atrophy, X-Linked 1	61	0.042

309	P	PRT013	Portal Hypertension	61	0.042

310		BRN056	Bronchopulmonary Dysplasia	60	0.042

311	P	INF032	Infertility	60	0.042

312		PLM010	Pulmonary Edema	59	0.042

313		PTT009	Pituitary Gland Disease	59	0.042

314		PNC034	Pancreas Disease	59	0.042

315		BRN004	Brain Edema	59	0.042

316		INT253	Intestinal Benign Neoplasm	57	0.042

317	P	RTN016	Retinal Degeneration	56	0.042

318	P	PTT006	Pituitary Adenoma	54	0.042

319		AMN003	Amnestic Disorder	53	0.042

320	c	HPT015	Hepatitis D	52	0.042

321	P	PRR002	Pure Red-Cell Aplasia	52	0.042

322		IDP024	Idiopathic Inflammatory Myopathy	52	0.042

323	c	PNC106	Pancreatic Agenesis 1	51	0.042

324		OCL069	Ocular Motor Apraxia	49	0.042

325		DNG001	Dengue Shock Syndrome	48	0.042

326		CRZ002	Crouzon Syndrome with Acanthosis Nigricans	46	0.042

327		SLT001	Solitary Osseous Plasmacytoma	44	0.042

328		ADR022	Adrenomyeloneuropathy	43	0.042

329		RCT017	Rectal Disease	43	0.042

330		MRP001	Morphine Dependence	42	0.042

331		ATM052	Autoimmune Disease 1	40	0.042

332	c	PCH010	Pachyonychia Congenita 3	40	0.042

333		CRB079	Cerebrospinal Fluid Leak	38	0.042

334		MYT011	Myotonia	34	0.042

335		PRN021	Paranasal Sinus Disease	32	0.042

336		BLD163	Blood Group, Dombrock System	27	0.042

337	c	MCL042	Macular Degeneration, Age-Related, 1	83	0.036

338	P	RSP003	Respiratory Failure	72	0.036

339	c	THR092	Thrombophilia Due to Thrombin Defect	69	0.036

340	P	HYP098	Hypereosinophilic Syndrome	67	0.036

341		RCK004	Rickets	66	0.036

342		LPD016	Lipoid Proteinosis of Urbach and Wiethe	66	0.036

343	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	66	0.036

344		MCC012	Mccune-Albright Syndrome	65	0.036

345		MLT118	Multiple Acyl-Coa Dehydrogenase Deficiency	64	0.036

346		CLR108	Colorectal Adenoma	64	0.036

347		INC002	Inclusion Body Myositis	63	0.036

348	P	FTL001	Fetal Alcohol Syndrome	63	0.036

349	P	BNC003	Bone Cancer	62	0.036

350		FCT002	Factor Xi Deficiency	62	0.036

351	P	BRG001	Brugada Syndrome	61	0.036

352		HPT019	Hepatic Encephalopathy	60	0.036

353		END041	Endometrial Adenocarcinoma	60	0.036

354		THY121	Thyroid Gland Anaplastic Carcinoma	59	0.036

355		ACT119	Acute Promyelocytic Leukemia	59	0.036

356	P	CTR002	Cataract	59	0.036

357	c	MCP004	Mucopolysaccharidosis Iv	59	0.036

358	c	PRT132	Protoporphyria, Erythropoietic, 1	58	0.036

359	P	PLY041	Polymyositis	58	0.036

360		PTT046	Pituitary Hormone Deficiency, Combined, 2	56	0.036

361	c	GLY004	Glycogen Storage Disease V	56	0.036

362	P	PMP001	Pemphigus	56	0.036

363	P	MSC003	Muscular Atrophy	56	0.036

364		CYS039	Cystic Kidney Disease	55	0.036

365		PLY023	Polycystic Liver Disease	55	0.036

366	P	LMB006	Limb-Girdle Muscular Dystrophy	55	0.036

367	P	END047	Endophthalmitis	54	0.036

368		MYL004	Myelodysplastic Myeloproliferative Cancer	54	0.036

369		ATY042	Atypical Chronic Myeloid Leukemia	53	0.036

370	P	MTC069	Mitochondrial Disorders	53	0.036

371		GNG002	Ganglioneuroma	53	0.036

372		GNG005	Gangliocytoma	52	0.036

373	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	52	0.036

374		ALC009	Alcoholic Liver Cirrhosis	52	0.036

375		LKC003	Leukocyte Disease	52	0.036

376	P	MTC133	Mitochondrial Myopathy	52	0.036

377		GRN017	Granulocytopenia	51	0.036

378		ISL001	Islet Cell Tumor	51	0.036

379		DRR003	Diarrhea 5, with Tufting Enteropathy, Congenital	50	0.036

380	P	RNL017	Renal Oncocytoma	50	0.036

381		CNG028	Congenital Hypoplastic Anemia	50	0.036

382	P	MYT023	Myotonia Congenita	49	0.036

383		RNL011	Renal Osteodystrophy	49	0.036

384		ACT017	Acute Chest Syndrome	48	0.036

385		HRT015	Heritable Pulmonary Arterial Hypertension	48	0.036

386		IDP073	Idiopathic Hypercalciuria	48	0.036

387		OCL052	Ocular Dominance	48	0.036

388	P	OLV001	Olivopontocerebellar Atrophy	48	0.036

389		SGW002	Segawa Syndrome, Autosomal Recessive	48	0.036

390		ANC002	Anca-Associated Vasculitis	47	0.036

391		DWR001	Dwarfism	47	0.036

392		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	47	0.036

393		NDL007	Nodular Goiter	47	0.036

394	P	END039	Endodermal Sinus Tumor	47	0.036

395		SKL017	Skeletal Dysplasias	46	0.036

396	c	ATS282	Autosomal Recessive Malignant Osteopetrosis	46	0.036

397	P	HYP263	Hypersomnia	45	0.036

398	P	MND003	Mandibuloacral Dysplasia with Type a Lipodystrophy	44	0.036

399		MYX004	Myxedema	43	0.036

400	P	HYP265	Hypotonia	43	0.036

401		BWN003	Bowenoid Papulosis	42	0.036

402		HYP026	Hypoglycemic Coma	42	0.036

403		ALC001	Alcohol-Related Birth Defect	42	0.036

404		IDP033	Idiopathic Edema	41	0.036

405		FML063	Familial Glucocorticoid Deficiency	41	0.036

406		SNL007	Senile Cataract	40	0.036

407		ADN022	Adenylosuccinase Deficiency	40	0.036

408		ACR002	Acrocapitofemoral Dysplasia	39	0.036

409		MYP001	Myoepithelioma	39	0.036

410	P	THP004	Thiopurines, Poor Metabolism of, 1	38	0.036

411		GGN002	Gigantism	36	0.036

412		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	35	0.036

413	c	PSD104	Pseudohypoparathyroidism, Type Ii	34	0.036

414	P	MRQ003	Morquio Syndrome	33	0.036

415	c	EPS039	Episodic Pain Syndrome, Familial, 1	31	0.036

416		PTT001	Pituitary Hypoplasia	29	0.036

417	c	PRS080	Prostate Cancer, Hereditary, 7	28	0.036

418		BLD151	Blood Group--Wright Antigen	26	0.036

419		CHR158	Charles Bonnet Syndrome	26	0.036

420		BLD153	Blood Group--Swann System	25	0.036

421		ACT096	Acute Cholinergic Dysautonomia	19	0.036

422		NCL008	Nuclear Ribonucleic Acid	15	0.036