Search results for FAD

241 hits were found for FAD

#	Family	MCID	Name	MIFTS	Score
1	P	FTL069	Fetal Akinesia Deformation Sequence 1	55	6.012

2		MLT118	Multiple Acyl-Coa Dehydrogenase Deficiency	64	2.717

3	c	ERL029	Early-Onset, Autosomal Dominant Alzheimer Disease	42	2.717

4	c	FTL070	Fetal Akinesia Deformation Sequence 2	33	0.267

5	P	ALZ034	Alzheimer Disease	90	0.156

6	c	FTL071	Fetal Akinesia Deformation Sequence 3	23	0.150

7		RBF001	Riboflavin Deficiency	46	0.102

8	P	HYP724	Hyperlipoproteinemia, Type Iii	74	0.093

9	P	CHR012	Chronic Granulomatous Disease	69	0.093

10	P	CRN018	Coronary Artery Anomaly	67	0.093

11	P	BDY004	Body Mass Index Quantitative Trait Locus 11	78	0.083

12		DRM006	Dermatitis	63	0.083

13		ART140	Arteries, Anomalies of	60	0.083

14	c	BDY020	Body Mass Index Quantitative Trait Locus 19	51	0.083

15	c	BDY021	Body Mass Index Quantitative Trait Locus 20	50	0.083

16	c	BDY005	Body Mass Index Quantitative Trait Locus 9	49	0.083

17	c	BDY010	Body Mass Index Quantitative Trait Locus 4	48	0.083

18	c	BDY015	Body Mass Index Quantitative Trait Locus 12	48	0.083

19	c	BDY019	Body Mass Index Quantitative Trait Locus 18	48	0.083

20	c	BDY011	Body Mass Index Quantitative Trait Locus 10	47	0.083

21	c	BDY017	Body Mass Index Quantitative Trait Locus 14	46	0.083

22	c	BDY006	Body Mass Index Quantitative Trait Locus 8	45	0.083

23	c	BDY012	Body Mass Index Quantitative Trait Locus 7	45	0.083

24		BCK006	Back Pain	44	0.083

25		ALK024	Alkuraya-Kucinskas Syndrome	41	0.083

26		CNG506	Congenital Amyoplasia	26	0.083

27	P	LYM118	Lymphoma	70	0.072

28		CLF027	Cleft Palate, Isolated	67	0.072

29		IRR002	Irritable Bowel Syndrome	65	0.072

30		ETN001	Eating Disorder	61	0.072

31		PLY012	Polyhydramnios	48	0.072

32	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	91	0.059

33	c	DLT002	Dilated Cardiomyopathy	81	0.059

34	c	ATR087	Atrial Standstill 1	76	0.059

35	P	ATS364	Autism	68	0.059

36	P	DRM053	Dermatitis, Atopic	68	0.059

37	P	MCR115	Microvascular Complications of Diabetes 5	67	0.059

38	P	CLC063	Celiac Disease 1	66	0.059

39		CHG001	Chagas Disease	66	0.059

40		LPD008	Lipid Metabolism Disorder	64	0.059

41	P	ENC018	Encephalopathy	64	0.059

42		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	63	0.059

43	P	PSR002	Psoriasis	63	0.059

44	P	MYP004	Myopathy	63	0.059

45		HYP066	Hyperglycemia	63	0.059

46	P	ANP001	Anaplastic Large Cell Lymphoma	62	0.059

47	P	CTR002	Cataract	62	0.059

48	P	SCL018	Scoliosis	61	0.059

49	P	MYC008	Myocarditis	60	0.059

50		IRN002	Iron Metabolism Disease	58	0.059

51		AGN016	Aging	58	0.059

52		TCL023	T-Cell Lymphoma, Subcutaneous Panniculitis-Like	57	0.059

53		CHR081	Choroideremia	54	0.059

54		PRP036	Peripheral T-Cell Lymphoma	53	0.059

55		MCL006	Macular Retinal Edema	52	0.059

56		ATX038	Ataxia and Polyneuropathy, Adult-Onset	51	0.059

57		PST011	Pustulosis of Palm and Sole	51	0.059

58		ATS010	Autosomal Recessive Disease	49	0.059

59		47X002	47,xyy	49	0.059

60		LYM019	Lymphosarcoma	48	0.059

61		DBT006	Diabetic Macular Edema	46	0.059

62		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.059

63		ACY011	Acyl-Coa Dehydrogenase Deficiency	38	0.059

64		PRN039	Paraneoplastic Syndromes	37	0.059

65		CND006	Candida Glabrata	33	0.059

66	P	CLR023	Colorectal Cancer	100	0.042

67	P	BRS047	Breast Cancer	99	0.042

68	c	HYP595	Hypertension, Essential	87	0.042

69		MYL069	Myeloma, Multiple	85	0.042

70		STR067	Stroke, Ischemic	82	0.042

71	P	HRT032	Heart Disease	78	0.042

72	P	NRF023	Neurofibromatosis, Type Ii	77	0.042

73	c	CWD006	Cowden Syndrome 1	76	0.042

74	P	EPL164	Epilepsy	73	0.042

75		PHN003	Phenylketonuria	73	0.042

76	P	HNT016	Huntington Disease	72	0.042

77		OTT002	Otitis Media	71	0.042

78	P	ART022	Arthritis	71	0.042

79	P	LVR013	Liver Disease	71	0.042

80		CRB039	Cerebrovascular Disease	71	0.042

81	P	HYP086	Hypothyroidism	70	0.042

82	c	ATS007	Autism Spectrum Disorder	69	0.042

83	P	MYC084	Mycobacterium Tuberculosis 1	69	0.042

84		LGH007	Leigh Syndrome	69	0.042

85	P	MJR001	Major Depressive Disorder	69	0.042

86	P	MYS003	Myasthenia Gravis	68	0.042

87	P	DMN002	Dementia	68	0.042

88		HYP056	Hypoglycemia	68	0.042

89		SKN019	Skin Melanoma	68	0.042

90		MLN008	Melanoma	68	0.042

91		CRP001	Carpal Tunnel Syndrome	68	0.042

92	c	CRB175	Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1	67	0.042

93	P	FLL037	Follicular Lymphoma	67	0.042

94	P	DBT009	Diabetes Mellitus	66	0.042

95		NPH091	Nephrolithiasis, Calcium Oxalate	66	0.042

96	P	MTR004	Maturity-Onset Diabetes of the Young	66	0.042

97		PRT037	Pertussis	66	0.042

98	P	PRS038	Personality Disorder	66	0.042

99	P	CWD010	Cowden Syndrome	66	0.042

100	P	NRB010	Neuroblastoma 1	66	0.042

101		DSS008	Disease of Mental Health	66	0.042

102		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	0.042

103		ANG054	Angina Pectoris	66	0.042

104	P	SPN046	Spinal Muscular Atrophy	65	0.042

105		DPR016	Depression	64	0.042

106		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.042

107	P	VSC011	Vasculitis	64	0.042

108		SKN016	Skin Disease	64	0.042

109		INT323	Intraocular Pressure Quantitative Trait Locus	64	0.042

110		ART002	Arts Syndrome	63	0.042

111	P	CNG001	Congenital Myasthenic Syndrome	63	0.042

112		FTT001	Fatty Liver Disease	63	0.042

113		LNG099	Lung Disease	62	0.042

114		ACY010	Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of	62	0.042

115		NNL005	Non-Alcoholic Fatty Liver Disease	62	0.042

116		THY029	Thyroid Carcinoma	62	0.042

117		STT001	Status Epilepticus	61	0.042

118	P	DST002	Distal Arthrogryposis	61	0.042

119		CRY035	Cryptorchidism, Unilateral or Bilateral	61	0.042

120		CHR066	Chronic Fatigue Syndrome	61	0.042

121		CRB172	Cerebral Amyloid Angiopathy, Cst3-Related	61	0.042

122	P	MYL006	Myeloid Leukemia	61	0.042

123		APP008	Appendicitis	61	0.042

124	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	61	0.042

125		PPT005	Peptic Ulcer Disease	60	0.042

126		MNT002	Mental Depression	60	0.042

127		LPT001	Leptospirosis	60	0.042

128		END030	End Stage Renal Failure	60	0.042

129	P	CRN300	Coronary Heart Disease 1	59	0.042

130		NRN004	Neuroendocrine Tumor	59	0.042

131	P	BPL003	Bipolar Disorder	59	0.042

132		CNS004	Constipation	59	0.042

133	P	SYP003	Syphilis	59	0.042

134	c	ACT210	Acute Respiratory Distress Syndrome	59	0.042

135		URN010	Urinary Tract Obstruction	59	0.042

136	P	PLY011	Polycystic Ovary Syndrome	58	0.042

137		CNT047	Contact Dermatitis	58	0.042

138	P	EXN002	Exanthem	58	0.042

139	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	58	0.042

140		CHL014	Cholera	58	0.042

141	P	SLP005	Sleep Disorder	58	0.042

142	P	INF037	Inflammatory Bowel Disease	57	0.042

143		BCT022	Bacterial Infectious Disease	57	0.042

144		APH002	Aphasia	56	0.042

145		ALL010	Allergic Contact Dermatitis	56	0.042

146	c	SVR001	Severe Acute Respiratory Syndrome	56	0.042

147		PRT038	Protein-Energy Malnutrition	56	0.042

148		AMN003	Amnestic Disorder	55	0.042

149	P	VNS003	Venous Insufficiency	55	0.042

150		HYP060	Hyperinsulinism	55	0.042

151	P	RST001	Restless Legs Syndrome	54	0.042

152	c	SCN036	Secondary Progressive Multiple Sclerosis	54	0.042

153		HMC014	Homocysteinemia	54	0.042

154	c	MTR020	Maturity-Onset Diabetes of the Young, Type 3	54	0.042

155		SPP010	Suppressor of Tumorigenicity 3	54	0.042

156	c	MTR019	Maturity-Onset Diabetes of the Young, Type 2	54	0.042

157		HYP014	Hyperuricemia	52	0.042

158		FDL002	Food Allergy	52	0.042

159		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.042

160	P	HMC002	Homocystinuria	52	0.042

161		DNT012	Dental Caries	52	0.042

162	P	CHR345	Chronic Pain	52	0.042

163	P	MYT002	Myotonic Dystrophy	52	0.042

164	P	MSC003	Muscular Atrophy	52	0.042

165		MCR088	Microscopic Polyangiitis	51	0.042

166		RST011	Restrictive Dermopathy, Lethal	51	0.042

167		STM007	Stomatitis	51	0.042

168	c	INH020	Inherited Metabolic Disorder	51	0.042

169		HYP748	Hypertelorism	50	0.042

170	P	DRM007	Dermatitis Herpetiformis	50	0.042

171		HYD012	Hydrops Fetalis	49	0.042

172	c	L2H001	L-2-Hydroxyglutaric Aciduria	49	0.042

173		THM002	Thiamine-Responsive Megaloblastic Anemia Syndrome	49	0.042

174	P	TRM004	Trimethylaminuria	49	0.042

175		PTH002	Pathological Gambling	48	0.042

176		CHR001	Churg-Strauss Syndrome	48	0.042

177		CYS002	Cystic Lymphangioma	47	0.042

178		ESN020	Eosinophilic Granulomatosis with Polyangiitis	47	0.042

179	c	ALZ056	Alzheimer Disease 3	47	0.042

180	c	CRV002	Cervix Uteri Carcinoma in Situ	47	0.042

181	P	MYC033	Myoclonus	47	0.042

182	P	MTH007	Methemoglobinemia	47	0.042

183		MCL027	Macular Dystrophy, Dominant Cystoid	47	0.042

184		CYT002	Cytokine Deficiency	46	0.042

185		HLX001	Helix Syndrome	46	0.042

186		FLL008	Folliculitis	46	0.042

187		KWS001	Kwashiorkor	46	0.042

188	c	ACT076	Acute Myocarditis	45	0.042

189		HMC041	Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity	45	0.042

190		RSP021	Respiratory Allergy	45	0.042

191	c	DRM054	Dermatitis, Atopic, 2	45	0.042

192		CYN002	Cyanosis, Transient Neonatal	45	0.042

193		MLK006	Milk Allergy	44	0.042

194		OBS082	Obstructive Nephropathy	44	0.042

195	c	ATS307	Autosomal Recessive Cerebellar Ataxia	44	0.042

196		ANC002	Anca-Associated Vasculitis	43	0.042

197		ANT003	Antley-Bixler Syndrome	43	0.042

198	c	PCH010	Pachyonychia Congenita 3	43	0.042

199	c	MJR024	Major Affective Disorder 9	42	0.042

200		GRD001	Giardiasis	42	0.042

201		CRV045	Cervical Intraepithelial Neoplasia	41	0.042

202		ARB001	Ariboflavinosis	41	0.042

203		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	41	0.042

204	c	MLT010	Multiple Personality Disorder	41	0.042

205		SPS019	Spastic Paraparesis	40	0.042

206	c	2HY001	2-Hydroxyglutaric Aciduria	40	0.042

207		URM005	Uremic Pruritus	40	0.042

208		CRN048	Craniofacial-Deafness-Hand Syndrome	39	0.042

209	c	MJR022	Major Affective Disorder 8	39	0.042

210		CVT001	Cavitary Optic Disc Anomalies	39	0.042

211	c	PLY105	Polycystic Ovary Syndrome 1	38	0.042

212		TBS001	Tabes Dorsalis	38	0.042

213		48X005	48,xyyy	37	0.042

214	c	DRM040	Dermatitis Herpetiformis, Familial	36	0.042

215		MLR009	Miliaria	35	0.042

216		AST003	Asthenopia	34	0.042

217		SPT023	Septate Uterus	34	0.042

218		RRS014	Rare Surgical Neurologic Disease	33	0.042

219		MLR001	Miliaria Rubra	32	0.042

220		CNG538	Congenital Arthrogryposis with Anterior Horn Cell Disease	30	0.042

221		FGF001	Fgfr-Related Craniosynostosis Syndromes	30	0.042

222		WHT017	Wheat Allergy	30	0.042

223		PTL002	Patellofemoral Pain Syndrome	30	0.042

224	c	HRD146	Hereditary Methemoglobinemia	29	0.042

225		ARG004	Argyria	28	0.042

226		CNG065	Congenital Contractures	28	0.042

227		MTC015	Mitochondrial Dna-Associated Leigh Syndrome and Narp	27	0.042

228		STN013	Stenotrophomonas Maltophilia Infection	26	0.042

229		ESN016	Eosinophilic Pustular Folliculitis	26	0.042

230	c	CNG223	Congenital Methemoglobinemia	25	0.042

231		MYT026	Myotonia Atrophica	25	0.042

232		ALL012	Allergic Angiitis	25	0.042

233		ALP089	Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality	24	0.042

234		NCL007	Nuclear Gene-Encoded Leigh Syndrome	24	0.042

235		FTL016	Fetal Edema	24	0.042

236		SYP005	Syphilitic Myelopathy	22	0.042

237		LPD042	Lipid Storage Myopathy Due to Flavin Adenine Dinucleotide Synthetase Deficiency	21	0.042

238		MTC166	Mitochondrial Complex I Deficiency, Nuclear Type 19	20	0.042

239	c	FTL072	Fetal Akinesia Deformation Sequence 4	20	0.042

240	c	PRM209	Primary Trimethylaminuria	19	0.042

241		ALP025	Alopecia, Epilepsy, Pyorrhea, Mental Subnormality	16	0.042