Search results for pbx1

#	Family	MCID	Name	MIFTS	Score
1		CNG495	Congenital Anomalies of Kidney and Urinary Tract Syndrome with or Without Hearing Loss, Abnormal Ears, or Developmental Delay	37	42.286

2		BLY008	B-Lymphoblastic Leukemia/lymphoma with Tcf3-Pbx1	16	35.528

3	P	LKM002	Leukemia	65	28.530

4	P	LKM062	Leukemia, Acute Lymphoblastic	69	20.739

5	c	BLY015	B-Lymphoblastic Leukemia/lymphoma with T(1;19)(q23;p13.3)	12	19.537

6	c	ACT073	Acute Leukemia	58	16.592

7	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	50	15.841

8	c	TYP009	Type 2 Diabetes Mellitus	91	10.787

9		CLF027	Cleft Palate, Isolated	63	10.192

10	P	DSR090	Disorder of Sexual Development	52	9.839

11	c	LKM061	Leukemia, Acute Myeloid	82	9.554

12		CKT002	Cakut	51	9.460

13		CHL061	Childhood Leukemia	43	9.058

14	c	ADL052	Adult Acute Lymphocytic Leukemia	45	8.854

15		RNL109	Renal Hypoplasia, Bilateral	19	8.781

16	c	DPH024	Diaphragmatic Hernia, Congenital	66	8.384

17	P	MYR002	Mayer-Rokitansky-Kuster-Hauser Syndrome	59	8.152

18		CYS013	Cystinuria	65	7.858

19	c	46X082	46,xy Sex Reversal	50	7.769

20	P	BCL013	B-Cell Adult Acute Lymphocytic Leukemia	36	7.332

21		MYP002	Myoepithelial Carcinoma	43	7.263

22		BLY005	B-Lymphoblastic Leukemia/lymphoma with Hyperdiploidy	22	7.134

23		BLY006	B-Lymphoblastic Leukemia/lymphoma with Hypodiploidy	23	7.134

24		BLY010	B-Lymphoblastic Leukemia/lymphoma with Iamp21	24	7.134

25		CHN056	Chondrosarcoma, Extraskeletal Myxoid	44	7.082