Search results for rxrg

81 hits were found for rxrg

#	Family	MCID	Name	MIFTS	Score
1	P	LNG032	Lung Cancer	98	21.851

2	P	HYP838	Hyperlipidemia, Familial Combined, 3	61	13.010

3	P	CNR004	Cone-Rod Dystrophy 2	74	12.616

4	P	RTN008	Retinitis Pigmentosa	79	8.921

5	P	BRS047	Breast Cancer	97	2.455

6		ADN018	Adenoma	58	1.263

7	P	PTT006	Pituitary Adenoma	55	1.182

8		PTT048	Pituitary Adenoma, Prolactin-Secreting	64	1.131

9		FML168	Familial Isolated Pituitary Adenoma	33	1.131

10	P	PNC035	Pancreatic Cancer	87	0.602

11		LPD008	Lipid Metabolism Disorder	61	0.509

12	P	CRN300	Coronary Heart Disease 1	73	0.426

13	c	MJR022	Major Affective Disorder 8	37	0.360

14	c	MJR024	Major Affective Disorder 9	40	0.360

15	P	SPR119	Spermatogenic Failure, X-Linked, 1	36	0.360

16	P	MLN007	Male Infertility	56	0.360

17	P	BPL003	Bipolar Disorder	56	0.360

18		TXC005	Toxic Shock Syndrome	61	0.360

19	P	INF032	Infertility	60	0.360

20		ANX010	Anxiety	70	0.322

21		RCK004	Rickets	64	0.322

22	P	END046	Endometritis	46	0.322

23	P	MLN008	Melanoma	75	0.322

24		THY029	Thyroid Carcinoma	55	0.322

25	P	MLN069	Melanoma, Uveal	59	0.279

26		FLL031	Follicular Adenoma	40	0.279

27		GST033	Gestational Diabetes	60	0.279

28		SKN019	Skin Melanoma	70	0.279

29	c	FTL070	Fetal Akinesia Deformation Sequence 2	36	0.228

30		CRY035	Cryptorchidism, Unilateral or Bilateral	57	0.228

31	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	0.228

32	P	HRT032	Heart Disease	84	0.228

33		ALL003	Allergic Rhinitis	66	0.161

34		AND014	Androgenic Alopecia	46	0.161

35	P	PRM051	Primary Pigmented Nodular Adrenocortical Disease	55	0.161

36		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	0.161

37		NRL016	Neural Tube Defects	80	0.161

38	P	ALP061	Alopecia, Androgenetic, 1	48	0.161

39	c	BRN108	Branchiootic Syndrome 1	63	0.161

40	c	DFN163	Deafness, Autosomal Dominant 7	31	0.161

41		AGN016	Aging	53	0.161

42	P	FML012	Familial Partial Lipodystrophy	54	0.161

43	c	MCR133	Microvascular Complications of Diabetes 4	41	0.161

44	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	0.161

45		CNG495	Congenital Anomalies of Kidney and Urinary Tract Syndrome with or Without Hearing Loss, Abnormal Ears, or Developmental Delay	26	0.161

46	c	MCR113	Microvascular Complications of Diabetes 3	52	0.161

47	c	MCR130	Microvascular Complications of Diabetes 6	41	0.161

48	c	MCR120	Microvascular Complications of Diabetes 7	47	0.161

49		HLX001	Helix Syndrome	47	0.161

50	c	THY107	Thymoma, Familial	42	0.161

51		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	0.161

52		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	0.161

53	P	MNR014	Menarche, Age at, Quantitative Trait Locus 2	7	0.161

54	c	MNR015	Menarche, Age at, Quantitative Trait Locus 3	6	0.161

55	c	AMY091	Amyotrophic Lateral Sclerosis 1	87	0.161

56		IGR001	Ige Responsiveness, Atopic	58	0.161

57	c	LPD015	Lipodystrophy, Familial Partial, Type 2	61	0.161

58		HMN044	Human Immunodeficiency Virus Type 1	76	0.161

59	P	THY023	Thymoma	64	0.161

60		END035	Endocrine Gland Cancer	42	0.161

61	P	LTR001	Lateral Sclerosis	57	0.161

62	P	MYP006	Myopia	55	0.161

63		RNL025	Renal Hypoplasia	46	0.161

64		NNL005	Non-Alcoholic Fatty Liver Disease	63	0.161

65	P	RHN004	Rhinitis	56	0.161

66		THY123	Thyroid Gland Follicular Carcinoma	53	0.161

67		ALL029	Allergic Disease	61	0.161

68	P	HYP040	Hypospadias	51	0.161

69	P	MCR010	Microcephaly	59	0.161

70	P	ART022	Arthritis	70	0.161

71		SCR011	Scrapie	39	0.161

72	P	PRN023	Prion Disease	60	0.161

73	P	NRF002	Neurofibromatosis	60	0.161

74		END086	End Stage Renal Disease	54	0.161

75		CYT002	Cytokine Deficiency	43	0.161

76		FTT001	Fatty Liver Disease	61	0.161

77	P	HYP076	Hyperthyroidism	53	0.161

78		DFF036	Differentiated Thyroid Carcinoma	51	0.161

79		ORL011	Oral Cancer	60	0.161

80	P	ALP008	Alopecia	53	0.161

81	P	ENC018	Encephalopathy	62	0.161