Search results for hoxa3

80 hits were found for hoxa3

#	Family	MCID	Name	MIFTS	Score
1		PNL012	Penile Cancer	57	11.938

2		HND004	Hand-Foot-Genital Syndrome	47	9.365

3		TCL025	T-Cell Immunodeficiency with Thymic Aplasia	42	8.442

4		DGR001	Digeorge Syndrome	62	8.442

5		ECT003	Ectopic Thymus	25	8.442

6		CNG005	Congenital Aphakia	23	8.442

7		PNL025	Penile Benign Neoplasm	31	8.442

8	P	LNG064	Lung Cancer Susceptibility 3	70	3.538

9	P	ADN016	Adenocarcinoma	63	3.538

10		LNG039	Lung Squamous Cell Carcinoma	57	3.460

11		CHR100	Chronic Ulcer of Skin	57	3.348

12		VTR016	Vater/vacterl Association	49	2.727

13		ESP020	Esophageal Atresia	60	2.727

14		VCT001	Vacterl Association	47	2.727

15		RNL114	Renal Cell Carcinoma, Nonpapillary	80	2.367

16		GLB002	Glioblastoma	67	2.367

17		CLR030	Clear Cell Renal Cell Carcinoma	54	2.367

18	P	LKM062	Leukemia, Acute Lymphoblastic	69	2.242

19		GLL048	Glial Tumor	52	2.228

20		LYM040	Lymphoblastic Lymphoma	53	2.228

21		GLM045	Glioma	63	2.228

22	P	GST053	Gastric Cancer	83	2.074

23	P	LKM002	Leukemia	67	2.074

24		HGH043	High Grade Glioma	45	2.074

25	P	LYM118	Lymphoma	67	1.899

26	P	MYC007	Myocardial Infarction	70	1.899

27		DSS032	Disease by Infectious Agent	55	1.899

28		THY029	Thyroid Carcinoma	51	1.899

29	c	ACT075	Acute Myocardial Infarction	56	1.899

30	c	HYP595	Hypertension, Essential	85	1.727

31		MLN065	Melanocytic Nevus Syndrome, Congenital	62	1.335

32		SKN019	Skin Melanoma	71	1.335

33		BRS099	Breast Ductal Carcinoma	61	1.335

34	c	LKM061	Leukemia, Acute Myeloid	83	1.306

35	c	DPH024	Diaphragmatic Hernia, Congenital	64	1.306

36	P	HYP040	Hypospadias	51	1.306

37	P	CLR023	Colorectal Cancer	100	1.204

38	P	PNC035	Pancreatic Cancer	86	1.204

39	P	ALZ034	Alzheimer Disease	87	1.131

40	P	MYL006	Myeloid Leukemia	61	1.131

41	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	0.923

42	P	NSP012	Nasopharyngeal Carcinoma	61	0.923

43	c	SPS128	Spastic Paraplegia 7, Autosomal Recessive	58	0.923

44		AGN016	Aging	54	0.923

45	c	DFN159	Deafness, Autosomal Dominant 5	31	0.923

46	c	RTN041	Retinitis Pigmentosa 11	42	0.923

47		CRY035	Cryptorchidism, Unilateral or Bilateral	58	0.923

48		OST012	Osteoarthritis	77	0.923

49	P	FML187	Familial Hypertension	34	0.923

50	P	BRS047	Breast Cancer	98	0.779

51	P	RRT020	Rare Tumor	39	0.653

52	P	OVR082	Overgrowth Syndrome	49	0.653

53		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	45	0.653

54		PLM134	Pulmonary Fibrosis, Idiopathic	76	0.653

55		ALP099	Alopecia, Congenital	23	0.653

56	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	0.653

57		ATS010	Autosomal Recessive Disease	42	0.653

58		DWN001	Down Syndrome	70	0.653

59		VLC001	Velocardiofacial Syndrome	57	0.653

60	c	TYP009	Type 2 Diabetes Mellitus	92	0.653

61		MNN043	Meningioma, Familial	79	0.653

62	P	SPN042	Spinal Cord Ependymoma	29	0.653

63		CLL010	Cellular Ependymoma	57	0.653

64		CRV025	Cervical Incompetence	35	0.653

65	P	ALP008	Alopecia	54	0.653

66		BCR002	Bicornuate Uterus	24	0.653

67		TRT001	Teratocarcinoma	42	0.653

68	P	PLM036	Pulmonary Fibrosis	66	0.653

69		SCR001	Secretory Meningioma	40	0.653

70		LYM002	Lymphoplasmacyte-Rich Meningioma	35	0.653

71		LNG099	Lung Disease	62	0.653

72	P	BNG030	Benign Ependymoma	51	0.653

73		CMB007	Combined Immunodeficiency	57	0.653

74	P	END044	Endometriosis	62	0.653

75		SVR004	Severe Combined Immunodeficiency	72	0.653

76		SPN021	Spinal Meningioma	50	0.653

77		ACT114	Acute Myeloblastic Leukemia Without Maturation	26	0.653

78		48X005	48,xyyy	39	0.653

79		HYP266	Hypoxia	57	0.653

80		CHR178	Chromosomal Triplication	34	0.653