Search results for hoxa3

87 hits were found for hoxa3

#	Family	MCID	Name	MIFTS	Score
1		PNL012	Penile Cancer	57	12.140

2		HND004	Hand-Foot-Genital Syndrome	48	8.811

3		DGR001	Digeorge Syndrome	62	8.584

4		PNL025	Penile Benign Neoplasm	31	8.584

5		ECT003	Ectopic Thymus	26	8.584

6		CNG005	Congenital Aphakia	23	8.584

7		CHR100	Chronic Ulcer of Skin	57	1.637

8	P	LKM062	Leukemia, Acute Lymphoblastic	69	1.542

9	P	LNG064	Lung Cancer Susceptibility 3	69	1.445

10	P	ADN016	Adenocarcinoma	63	1.445

11		LNG039	Lung Squamous Cell Carcinoma	57	1.426

12		MLN065	Melanocytic Nevus Syndrome, Congenital	62	1.331

13		BRS099	Breast Ductal Carcinoma	61	1.331

14		SKN019	Skin Melanoma	70	1.331

15		VTR016	Vater/vacterl Association	50	1.246

16		ESP020	Esophageal Atresia	59	1.246

17		VCT001	Vacterl Association	46	1.246

18		RNL114	Renal Cell Carcinoma, Nonpapillary	79	1.157

19		GLB002	Glioblastoma	67	1.157

20		CLR030	Clear Cell Renal Cell Carcinoma	53	1.157

21		LYM040	Lymphoblastic Lymphoma	53	1.123

22		GLM045	Glioma	62	1.123

23		GLL048	Glial Tumor	51	1.123

24	P	GST053	Gastric Cancer	82	1.085

25	P	LKM002	Leukemia	65	1.085

26		HGH043	High Grade Glioma	46	1.085

27		HPT022	Hepatoblastoma	54	1.085

28	P	LYM118	Lymphoma	66	1.042

29		DSS032	Disease by Infectious Agent	55	1.042

30	P	MYC007	Myocardial Infarction	69	1.042

31	c	ACT075	Acute Myocardial Infarction	55	1.042

32		THY029	Thyroid Carcinoma	55	1.042

33	P	BRS047	Breast Cancer	97	0.939

34	P	CLR023	Colorectal Cancer	100	0.778

35	P	PNC035	Pancreatic Cancer	87	0.711

36	c	HYP595	Hypertension, Essential	84	0.424

37	P	ALZ034	Alzheimer Disease	87	0.359

38	c	LKM061	Leukemia, Acute Myeloid	83	0.321

39	c	DPH024	Diaphragmatic Hernia, Congenital	63	0.321

40	P	HYP040	Hypospadias	51	0.321

41	c	HMP012	Hemophagocytic Lymphohistiocytosis, Familial, 2	47	0.278

42		SVR004	Severe Combined Immunodeficiency	70	0.278

43	P	MYL006	Myeloid Leukemia	60	0.278

44	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	0.227

45	c	EPD076	Epidermolysis Bullosa Dystrophica, Autosomal Recessive	51	0.227

46		CRY035	Cryptorchidism, Unilateral or Bilateral	57	0.227

47		AGN016	Aging	53	0.227

48	P	NSP012	Nasopharyngeal Carcinoma	60	0.227

49	c	SPS128	Spastic Paraplegia 7, Autosomal Recessive	58	0.227

50	c	DFN159	Deafness, Autosomal Dominant 5	31	0.227

51	c	RTN041	Retinitis Pigmentosa 11	43	0.227

52	P	RCS002	Recessive Dystrophic Epidermolysis Bullosa	62	0.227

53	P	EPD016	Epidermolysis Bullosa	53	0.227

54	P	EPD009	Epidermolysis Bullosa Dystrophica	66	0.227

55		SKN016	Skin Disease	63	0.227

56		OST012	Osteoarthritis	77	0.227

57	P	FML187	Familial Hypertension	34	0.227

58		PLM134	Pulmonary Fibrosis, Idiopathic	76	0.160

59		VLC001	Velocardiofacial Syndrome	57	0.160

60		DWN001	Down Syndrome	70	0.160

61	c	TYP009	Type 2 Diabetes Mellitus	91	0.160

62	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	58	0.160

63		ATS010	Autosomal Recessive Disease	42	0.160

64		ALP099	Alopecia, Congenital	23	0.160

65		MNN043	Meningioma, Familial	79	0.160

66		CMB007	Combined Immunodeficiency	56	0.160

67	P	BNG030	Benign Ependymoma	51	0.160

68		LYM002	Lymphoplasmacyte-Rich Meningioma	35	0.160

69		CLL010	Cellular Ependymoma	58	0.160

70	P	SPN042	Spinal Cord Ependymoma	30	0.160

71	P	END044	Endometriosis	62	0.160

72		SCR001	Secretory Meningioma	40	0.160

73	P	PLM036	Pulmonary Fibrosis	65	0.160

74		TRT001	Teratocarcinoma	41	0.160

75		INT395	Intracranial Meningioma	47	0.160

76		CRV025	Cervical Incompetence	35	0.160

77		LNG099	Lung Disease	62	0.160

78		48X005	48,xyyy	39	0.160

79		ORL011	Oral Cancer	60	0.160

80	P	ALP008	Alopecia	53	0.160

81		CHR178	Chromosomal Triplication	33	0.160

82		ACT114	Acute Myeloblastic Leukemia Without Maturation	26	0.160

83	P	RRT020	Rare Tumor	39	0.160

84		HYP266	Hypoxia	56	0.160

85		BCR002	Bicornuate Uterus	24	0.160

86	P	OVR082	Overgrowth Syndrome	41	0.160

87		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	44	0.160