Search results for cap2

51 hits were found for cap2

#	Family	MCID	Name	MIFTS	Score
1		FML304	Familial Isolated Dilated Cardiomyopathy	49	9.407

2	c	DLT002	Dilated Cardiomyopathy	78	5.265

3		CRD132	Cardiac Conduction Defect	60	4.759

4	P	GST053	Gastric Cancer	83	4.707

5	c	ATR087	Atrial Standstill 1	74	4.516

6	P	MLN008	Melanoma	76	4.447

7	P	HPT023	Hepatocellular Carcinoma	96	3.862

8	P	OVR042	Ovarian Cancer	88	3.187

9		GLL048	Glial Tumor	52	3.027

10		GLM045	Glioma	63	3.027

11		MCR013	Microphthalmia	60	2.913

12		OVR094	Ovarian Epithelial Cancer	39	2.614

13		NDL001	Nodular Malignant Melanoma	45	2.420

14	P	MYP004	Myopathy	67	2.380

15	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	2.317

16		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	2.317

17	c	MJR022	Major Affective Disorder 8	38	2.215

18	c	MJR024	Major Affective Disorder 9	41	2.215

19	P	BPL003	Bipolar Disorder	56	2.215

20		TRN015	Transient Cerebral Ischemia	63	2.095

21	P	VSC007	Vascular Disease	63	2.095

22	P	PNM007	Pneumonia	67	1.562

23		LNG111	Lung Non-Squamous Non-Small Cell Carcinoma	56	1.442

24	P	LNG021	Lung Occult Small Cell Carcinoma	20	1.442

25		LNG019	Lung Combined Type Small Cell Carcinoma	32	1.442

26	P	PNC035	Pancreatic Cancer	86	1.272

27		ALL029	Allergic Disease	59	1.210

28	P	BND020	Bone Disease	59	1.210

29	P	HRP006	Herpes Simplex	65	0.988

30	P	RNV001	Renovascular Hypertension	49	0.988

31	P	ATR011	Atrial Fibrillation	66	0.857

32	c	FML001	Familial Atrial Fibrillation	65	0.857

33	P	BRS047	Breast Cancer	98	0.811

34		ACR009	Acromesomelic Dysplasia, Hunter-Thompson Type	41	0.698

35	c	DFN137	Deafness, Autosomal Dominant 13	32	0.698

36	c	DFN154	Deafness, Autosomal Dominant 31	22	0.698

37		PRP027	Peripheral Vascular Disease	71	0.698

38		ALV005	Alveolar Soft Part Sarcoma	61	0.698

39		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	0.698

40		MYL005	Myelofibrosis	71	0.698

41		PLY001	Polycythemia Vera	69	0.698

42	P	PRS040	Prostate Cancer	95	0.698

43	c	DFN150	Deafness, Autosomal Dominant 21	24	0.698

44		TRM010	Traumatic Brain Injury	51	0.698

45	P	PLY018	Polycythemia	56	0.698

46		CMB007	Combined Immunodeficiency	57	0.698

47	P	ESS003	Essential Thrombocythemia	69	0.698

48		CNG034	Congestive Heart Failure	69	0.698

49		SVR004	Severe Combined Immunodeficiency	72	0.698

50		CHL068	Cholestasis	61	0.698

51		BRN071	Brain Injury	50	0.698