Search results for ITD 1

44 hits were found for ITD 1

#	Family	MCID	Name	MIFTS	Score
1	c	LKM061	Leukemia, Acute Myeloid	84	0.389

2	P	MYL006	Myeloid Leukemia	60	0.363

3	P	LKM002	Leukemia	68	0.178

4	P	CRD119	Cardiac Arrest	67	0.148

5		MYL069	Myeloma, Multiple	85	0.123

6	P	HYP086	Hypothyroidism	69	0.120

7		ATS010	Autosomal Recessive Disease	48	0.120

8		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.112

9	c	BRN108	Branchiootic Syndrome 1	62	0.111

10		ACT119	Acute Promyelocytic Leukemia	63	0.109

11	P	KDN017	Kidney Cancer	60	0.107

12		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.106

13		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.106

14	c	CHR064	Chronic Monocytic Leukemia	33	0.105

15		PLS009	Plasma Cell Neoplasm	51	0.105

16	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.103

17		CYT019	Cytogenetically Normal Acute Myeloid Leukemia	33	0.098

18		FCT007	Factor Vii Deficiency	67	0.096

19	P	EXN002	Exanthem	57	0.096

20		GTR002	Goiter	53	0.096

21		CHR178	Chromosomal Triplication	35	0.094

22		CRB039	Cerebrovascular Disease	67	0.093

23		STR067	Stroke, Ischemic	81	0.092

24	c	CNG006	Congenital Hypothyroidism	64	0.088

25	P	DYS154	Dystonia	65	0.086

26	c	LKM063	Leukemia, Chronic Myeloid	72	0.085

27		SPL018	Splenomegaly	48	0.081

28		CRD132	Cardiac Conduction Defect	58	0.081

29		CVD001	Covid-19	44	0.079

30		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.079

31		MYL031	Myeloproliferative Neoplasm	66	0.072

32		PNC001	Pancytopenia	54	0.071

33		PRT058	Pure Autonomic Failure	59	0.070

34	P	RRT020	Rare Tumor	41	0.067

35		MSN004	Mesenchymal Cell Neoplasm	41	0.066

36	c	DYS191	Dystonia 1, Torsion, Autosomal Dominant	50	0.065

37	P	MST009	Mastocytosis	64	0.064

38		CHL149	Childhood Acute Myeloid Leukemia	44	0.062

39	c	CLR017	Clear Cell Sarcoma	45	0.061

40	c	SYS004	Systemic Mastocytosis	63	0.060

41		ACT114	Acute Myeloblastic Leukemia Without Maturation	33	0.060

42	c	ORT011	Orthostatic Hypotension 1	44	0.059

43		ACT162	Acute Sensory Ataxic Neuropathy	26	0.058

44		LNG105	Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome	37	0.057