Search results for NADP

97 hits were found for NADP

#	Family	MCID	Name	MIFTS	Score
1		HLX001	Helix Syndrome	47	0.170

2	P	GLM045	Glioma	63	0.107

3	P	CTR002	Cataract	60	0.107

4		HYP266	Hypoxia	57	0.107

5		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.107

6		LPT001	Leptospirosis	66	0.093

7	P	HML002	Hemolytic Anemia	63	0.093

8		FTT001	Fatty Liver Disease	61	0.093

9	P	TXP001	Toxoplasmosis	60	0.093

10		GLL048	Glial Tumor	45	0.093

11		24D001	2,4-Dienoyl-Coa Reductase Deficiency	34	0.093

12		MLR004	Malaria	81	0.076

13		GLB015	Glioblastoma Multiforme	75	0.076

14	P	NRB001	Neuroblastoma	72	0.076

15	P	MYC084	Mycobacterium Tuberculosis 1	68	0.076

16		HYP056	Hypoglycemia	66	0.076

17		PRT037	Pertussis	65	0.076

18	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.076

19		HYP066	Hyperglycemia	61	0.076

20	P	MYC008	Myocarditis	59	0.076

21		CHL014	Cholera	59	0.076

22		ISC004	Ischemia	58	0.076

23	P	AST007	Astrocytoma	51	0.076

24	P	PLL002	Pellagra	46	0.076

25		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.076

26		ANX004	Anoxia	40	0.076

27		PPL052	Papillomatosis, Confluent and Reticulated	33	0.076

28		CND006	Candida Glabrata	32	0.076

29		PST092	Posttransplant Acute Limbic Encephalitis	29	0.076

30	P	CLR023	Colorectal Cancer	99	0.054

31	P	GLM040	Glioma Susceptibility 1	81	0.054

32		MSC157	Muscular Dystrophy, Duchenne Type	72	0.054

33		PLM001	Pulmonary Tuberculosis	69	0.054

34	P	MLN008	Melanoma	69	0.054

35	c	BSL007	Basal Cell Carcinoma	68	0.054

36		RCK004	Rickets	68	0.054

37	P	MSC005	Muscular Dystrophy	66	0.054

38		CRN036	Craniopharyngioma	65	0.054

39		ATH013	Atherosclerosis Susceptibility	65	0.054

40		CLN015	Colon Adenocarcinoma	65	0.054

41	P	VSC007	Vascular Disease	63	0.054

42	P	PSR002	Psoriasis	62	0.054

43		TXC005	Toxic Shock Syndrome	62	0.054

44		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.054

45		DRM006	Dermatitis	61	0.054

46	P	ENC018	Encephalopathy	61	0.054

47		LNG099	Lung Disease	60	0.054

48	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.054

49		INS001	Insulinoma	60	0.054

50		QFV001	Q Fever	60	0.054

51		GRD007	Grade Iii Astrocytoma	59	0.054

52		ADN018	Adenoma	59	0.054

53		ANT024	Anthrax Disease	58	0.054

54	P	URT039	Urticaria	58	0.054

55		IRN002	Iron Metabolism Disease	57	0.054

56		AGN016	Aging	56	0.054

57		HYP005	Hypokalemia	55	0.054

58		DBT010	Diabetic Neuropathy	54	0.054

59		HMS001	Hemosiderosis	54	0.054

60	P	RTN016	Retinal Degeneration	53	0.054

61		NNT012	Neonatal Jaundice	53	0.054

62	c	MCR113	Microvascular Complications of Diabetes 3	52	0.054

63	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.054

64		PST011	Pustulosis of Palm and Sole	52	0.054

65		OCL069	Ocular Motor Apraxia	51	0.054

66	P	HRD144	Hereditary Mixed Polyposis Syndrome	51	0.054

67	P	LCT001	Lactic Acidosis	51	0.054

68		CCC002	Coccidiosis	51	0.054

69		ANM045	Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency	49	0.054

70		VLV047	Volvulus of Midgut	49	0.054

71		47X002	47,xyy	49	0.054

72	P	CTN015	Cutaneous T Cell Lymphoma	49	0.054

73	c	MCR120	Microvascular Complications of Diabetes 7	47	0.054

74	P	CRC039	Coarctation of Aorta	47	0.054

75		RTN023	Retinitis	46	0.054

76	P	TRM004	Trimethylaminuria	46	0.054

77	c	MLG068	Malignant Glioma	46	0.054

78		GRD001	Giardiasis	45	0.054

79		MYX004	Myxedema	43	0.054

80		DVR002	Diverticulitis	43	0.054

81	P	HYP265	Hypotonia	43	0.054

82		HMP009	Haemophilus Influenzae	43	0.054

83		SNL007	Senile Cataract	42	0.054

84		NRR001	Neuroretinitis	42	0.054

85	P	HYP769	Hyperlysinemia, Type I	41	0.054

86	c	MCR130	Microvascular Complications of Diabetes 6	41	0.054

87	c	MCR133	Microvascular Complications of Diabetes 4	41	0.054

88	P	RRH023	Rare Hereditary Hemochromatosis	41	0.054

89		48X005	48,xyyy	39	0.054

90		HYP026	Hypoglycemic Coma	36	0.054

91		PYR009	Pyridoxine Deficiency Anemia	34	0.054

92		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.054

93		CYT014	Cytochrome P450 Oxidoreductase Deficiency	32	0.054

94		CMB083	Combined Immunodeficiency and Megaloblastic Anemia with or Without Hyperhomocysteinemia	28	0.054

95	c	RNG015	Ring Chromosome 2	26	0.054

96		CRT066	Cortisone Reductase Deficiency 2	24	0.054

97	c	PRM209	Primary Trimethylaminuria	18	0.054