Search results for tbx20

89 hits were found for tbx20

#	Family	MCID	Name	MIFTS	Score
1	c	ATR031	Atrial Septal Defect 4	30	40.897

2		INT276	Interatrial Communication	51	22.038

3	c	DLT002	Dilated Cardiomyopathy	78	21.012

4		HYP223	Hypoplastic Right Heart Syndrome	32	20.510

5		PTN001	Patent Foramen Ovale	62	20.330

6	P	HYP055	Hypoplastic Left Heart Syndrome	65	19.344

7	P	HRT032	Heart Disease	81	17.803

8		WLF001	Wolff-Parkinson-White Syndrome	65	16.482

9	P	TTR001	Tetralogy of Fallot	69	16.140

10	c	ART115	Aortic Valve Disease 1	74	13.731

11		HRT011	Heart Septal Defect	49	13.375

12	P	VNT002	Ventricular Septal Defect	58	13.014

13		DBL002	Double Outlet Right Ventricle	57	12.432

14	P	ATR010	Atrial Heart Septal Defect	58	12.387

15		LPP008	Lipoprotein Quantitative Trait Locus	65	9.773

16	c	HYP543	Hypoplastic Left Heart Syndrome 1	46	9.572

17		TRC062	Tricuspid Atresia	55	7.862

18	P	ATR001	Atrioventricular Septal Defect	55	7.862

19	P	PTN014	Patent Ductus Arteriosus 1	59	7.862

20		ULN003	Ulnar-Mammary Syndrome	56	7.583

21	P	ATR066	Atrial Septal Defect 2	42	6.910

22		CHR101	Char Syndrome	53	6.910

23		RGH009	Right Atrial Isomerism	57	6.910

24	P	TRC087	Tricuspid Valve Disease	48	6.910

25	c	ATR034	Atrial Septal Defect 6	29	6.910

26		RSP023	Rasopathy	53	6.910

27		CHR103	Charge Syndrome	66	6.910

28		HLT001	Holt-Oram Syndrome	66	6.910

29	c	HRM007	Hermansky-Pudlak Syndrome 4	46	6.910

30	c	MCR241	Microphthalmia, Syndromic 3	55	6.910

31		EBS001	Ebstein Anomaly	55	6.910

32		VLC001	Velocardiofacial Syndrome	57	6.910

33		DGR001	Digeorge Syndrome	62	6.910

34		JCB001	Jacobsen Syndrome	50	6.910

35	P	LFT003	Left Ventricular Noncompaction	57	6.910

36	P	PLM040	Pulmonary Valve Disease	40	6.910

37		PLM041	Pulmonary Valve Stenosis	50	6.910

38		LTM001	Lutembacher's Syndrome	23	6.910

39	c	ATR087	Atrial Standstill 1	74	5.894

40		CRD132	Cardiac Conduction Defect	60	4.394

41		CNG034	Congestive Heart Failure	69	3.588

42		CNT061	Conotruncal Heart Malformations	66	3.496

43	P	MYC007	Myocardial Infarction	70	3.448

44		LMB062	Limb Ischemia	55	3.088

45	P	LNG028	Long Qt Syndrome	64	2.884

46		BLP046	Blepharophimosis, Ptosis, and Epicanthus Inversus	56	2.405

47	P	RTN008	Retinitis Pigmentosa	80	2.405

48		NRR001	Neuroretinitis	42	2.405

49		BLP004	Blepharophimosis	36	2.405

50		RTN023	Retinitis	46	2.405

51		HLX001	Helix Syndrome	48	2.261

52		HYP066	Hyperglycemia	61	1.708

53	P	MTR012	Mitral Valve Disease	57	1.708

54		DSS032	Disease by Infectious Agent	55	1.166

55		SNG003	Single Ventricular Heart	30	0.952

56	P	ATS364	Autism	69	0.673

57		ATH013	Atherosclerosis Susceptibility	63	0.673

58	c	ORF037	Orofaciodigital Syndrome I	59	0.673

59		CRV035	Cervical Cancer	73	0.673

60		MCR037	Macroglossia	44	0.673

61		PLY150	Polykaryocytosis Inducer	29	0.673

62	P	BCK002	Beckwith-Wiedemann Syndrome	62	0.673

63	P	APL001	Aplastic Anemia	73	0.673

64	P	MGL010	Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a	40	0.673

65		UMB002	Umbilical Hernia	47	0.673

66		NRL016	Neural Tube Defects	81	0.673

67	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.673

68	c	VNT027	Ventricular Tachycardia, Catecholaminergic Polymorphic, 3	33	0.673

69	P	SPP010	Suppressor of Tumorigenicity 3	51	0.673

70	P	CNG499	Congenital Anomalies of Kidney and Urinary Tract 2	52	0.673

71	P	NNN008	Noonan Syndrome 1	77	0.673

72	P	CTC001	Catecholaminergic Polymorphic Ventricular Tachycardia	63	0.673

73		ADN012	Adenocarcinoma in Situ	43	0.673

74	P	CRV031	Cervical Adenocarcinoma	48	0.673

75	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.673

76	P	LNG064	Lung Cancer Susceptibility 3	70	0.673

77	P	ADN016	Adenocarcinoma	63	0.673

78		FCL012	Facial Paralysis	49	0.673

79	c	PSD047	Pseudo-Turner Syndrome	52	0.673

80	P	BRS047	Breast Cancer	98	0.602

81	P	PNC035	Pancreatic Cancer	86	0.602

82	c	GLM047	Glioma Susceptibility 3	33	0.464

83	c	MSM022	Mismatch Repair Cancer Syndrome 1	70	0.464

84	c	GLM025	Glioma Susceptibility 2	30	0.464

85	c	GLM043	Glioma Susceptibility 9	30	0.464

86	P	GLM040	Glioma Susceptibility 1	71	0.464

87		MNN043	Meningioma, Familial	79	0.464

88	P	OLG002	Oligodendroglioma	66	0.464

89		GLM045	Glioma	63	0.464