Search results for NADP

93 hits were found for NADP

#	Family	MCID	Name	MIFTS	Score
1		HLX001	Helix Syndrome	46	0.173

2	P	GLM045	Glioma	64	0.110

3	P	CTR002	Cataract	62	0.110

4		HYP266	Hypoxia	58	0.110

5		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.110

6	P	HML002	Hemolytic Anemia	64	0.095

7		FTT001	Fatty Liver Disease	63	0.095

8	P	TXP001	Toxoplasmosis	61	0.095

9		LPT001	Leptospirosis	60	0.095

10		GLL048	Glial Tumor	48	0.095

11		24D001	2,4-Dienoyl-Coa Reductase Deficiency	32	0.095

12		MLR004	Malaria	82	0.078

13		GLB002	Glioblastoma	74	0.078

14	P	MYC084	Mycobacterium Tuberculosis 1	69	0.078

15		HYP056	Hypoglycemia	68	0.078

16		PRT037	Pertussis	66	0.078

17	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	65	0.078

18		HYP066	Hyperglycemia	63	0.078

19		ISC004	Ischemia	62	0.078

20		GLB015	Glioblastoma Multiforme	60	0.078

21	P	MYC008	Myocarditis	60	0.078

22		CHL014	Cholera	58	0.078

23	P	AST007	Astrocytoma	52	0.078

24		ATX038	Ataxia and Polyneuropathy, Adult-Onset	51	0.078

25	P	PLL002	Pellagra	47	0.078

26		ANX004	Anoxia	44	0.078

27		PPL052	Papillomatosis, Confluent and Reticulated	34	0.078

28		PST092	Posttransplant Acute Limbic Encephalitis	29	0.078

29	P	CLR023	Colorectal Cancer	100	0.055

30		PLM001	Pulmonary Tuberculosis	72	0.055

31		MSC157	Muscular Dystrophy, Duchenne Type	70	0.055

32		RCK004	Rickets	70	0.055

33	P	MSC005	Muscular Dystrophy	68	0.055

34	c	BSL007	Basal Cell Carcinoma	68	0.055

35	P	NRB010	Neuroblastoma 1	66	0.055

36	P	VSC007	Vascular Disease	65	0.055

37		CRN036	Craniopharyngioma	65	0.055

38		CLN015	Colon Adenocarcinoma	65	0.055

39	P	ENC018	Encephalopathy	64	0.055

40		DRM006	Dermatitis	63	0.055

41	P	PSR002	Psoriasis	63	0.055

42		TXC005	Toxic Shock Syndrome	63	0.055

43		LNG099	Lung Disease	62	0.055

44		NNL005	Non-Alcoholic Fatty Liver Disease	62	0.055

45	P	URT039	Urticaria	61	0.055

46		INS001	Insulinoma	60	0.055

47		ADN018	Adenoma	60	0.055

48		GRD007	Grade Iii Astrocytoma	59	0.055

49	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	58	0.055

50		IRN002	Iron Metabolism Disease	58	0.055

51		AGN016	Aging	58	0.055

52		ANT024	Anthrax Disease	56	0.055

53	P	RTN016	Retinal Degeneration	56	0.055

54		DBT010	Diabetic Neuropathy	56	0.055

55	c	MCR113	Microvascular Complications of Diabetes 3	55	0.055

56		HYP005	Hypokalemia	55	0.055

57		HMS001	Hemosiderosis	54	0.055

58		OCL069	Ocular Motor Apraxia	53	0.055

59	P	CTN015	Cutaneous T Cell Lymphoma	52	0.055

60	P	LCT001	Lactic Acidosis	52	0.055

61		PST011	Pustulosis of Palm and Sole	51	0.055

62		47X002	47,xyy	49	0.055

63	P	TRM004	Trimethylaminuria	49	0.055

64	c	MCR120	Microvascular Complications of Diabetes 7	48	0.055

65		NNT012	Neonatal Jaundice	48	0.055

66		ANM045	Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency	47	0.055

67		RTN023	Retinitis	46	0.055

68		NRR001	Neuroretinitis	46	0.055

69		HMP009	Haemophilus Influenzae	46	0.055

70	c	MLG068	Malignant Glioma	46	0.055

71		CCC002	Coccidiosis	46	0.055

72		ART031	Aortic Coarctation	45	0.055

73		DVR002	Diverticulitis	44	0.055

74		INT052	Intestinal Volvulus	44	0.055

75	P	HYP265	Hypotonia	43	0.055

76	c	MCR130	Microvascular Complications of Diabetes 6	42	0.055

77	c	MCR133	Microvascular Complications of Diabetes 4	42	0.055

78		SNL007	Senile Cataract	41	0.055

79		MYX004	Myxedema	41	0.055

80		HYP026	Hypoglycemic Coma	41	0.055

81	P	RRH023	Rare Hereditary Hemochromatosis	41	0.055

82	P	HYP769	Hyperlysinemia, Type I	38	0.055

83	P	HRD144	Hereditary Mixed Polyposis Syndrome	38	0.055

84		48X005	48,xyyy	37	0.055

85		TRD008	Triiodothyronine Receptor Auxiliary Protein	35	0.055

86		CND006	Candida Glabrata	33	0.055

87		CYT014	Cytochrome P450 Oxidoreductase Deficiency	33	0.055

88		PYR009	Pyridoxine Deficiency Anemia	32	0.055

89	c	RNG015	Ring Chromosome 2	27	0.055

90		OBS168	Obsolete: Atypical Teratoid/rhabdoid Tumor	25	0.055

91		CRT066	Cortisone Reductase Deficiency 2	24	0.055

92		CMB083	Combined Immunodeficiency and Megaloblastic Anemia with or Without Hyperhomocysteinemia	23	0.055

93	c	PRM209	Primary Trimethylaminuria	19	0.055