Search results for ZNF469

51 hits were found for ZNF469

#	Family	MCID	Name	MIFTS	Score
1	P	BRT047	Brittle Cornea Syndrome	42	65.951

2	c	BRT028	Brittle Cornea Syndrome 1	39	61.623

3	c	KRT029	Keratoconus 1	31	30.854

4	P	KRT007	Keratoconus	50	25.621

5	P	MYP006	Myopia	56	19.067

6	P	EHL001	Ehlers-Danlos Syndrome	58	13.559

7		RFR003	Refractive Error	41	12.360

8	P	SCL018	Scoliosis	57	11.994

9	P	CRN276	Corneal Endothelial Dystrophy	53	10.574

10		BRT054	Brittle Bone Disorder	74	9.679

11	c	GLC092	Glaucoma, Primary Open Angle	62	9.607

12		FCH001	Fuchs' Endothelial Dystrophy	50	8.187

13		MRT007	Martsolf Syndrome	48	7.477

14	P	ANT088	Anterior Segment Dysgenesis	55	7.477

15	P	CRN024	Corneal Disease	44	7.477

16		RGL001	Regular Astigmatism	19	7.477

17		CRN009	Corneal Ectasia	29	7.477

18		IRR001	Irregular Astigmatism	32	7.477

19	P	AXN002	Axenfeld-Rieger Syndrome	63	7.477

20	P	CLL015	Collagen Disease	48	7.477

21		HYP706	Hypermobile Ehlers-Danlos Syndrome	55	7.227

22		ATS010	Autosomal Recessive Disease	42	3.857

23		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	3.343

24	P	OPN001	Open-Angle Glaucoma	55	3.138

25		GST092	Gastroesophageal Reflux	61	2.727

26		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	2.694

27		BNN005	Bunion	31	2.336

28	P	STC001	Stickler Syndrome	60	2.203

29		PHN003	Phenylketonuria	76	1.787

30		CNN005	Connective Tissue Disease	67	1.787

31	P	SNS001	Sensorineural Hearing Loss	59	1.787

32	P	HYP265	Hypotonia	42	1.492

33	c	BRN108	Branchiootic Syndrome 1	62	1.421

34		RTN017	Retinal Detachment	60	1.230

35		INT323	Intraocular Pressure Quantitative Trait Locus	64	1.230

36		HRW001	Hair Whorl	35	1.230

37	c	BRT029	Brittle Cornea Syndrome 2	33	1.004

38	P	DVL012	Developmental Dysplasia of the Hip 1	46	1.004

39	P	EYD002	Eye Disease	57	1.004

40	P	CRN025	Corneal Dystrophy	49	1.004

41	c	B4G002	B4galt7-Related Spondylodysplastic Ehlers-Danlos Syndrome	35	0.710

42		MRF001	Marfan Syndrome	76	0.710

43	c	ALB021	Albinism, Oculocutaneous, Type Ii	59	0.710

44		ESP021	Esophageal Cancer	83	0.710

45	c	EHL085	Ehlers-Danlos Syndrome, Spondylodysplastic Type, 2	46	0.710

46	c	CTS044	Cutis Laxa, Autosomal Recessive, Type Iic	24	0.710

47	c	EHL089	Ehlers-Danlos Syndrome, Classic-Like, 2	26	0.710

48	P	ADN016	Adenocarcinoma	63	0.710

49	P	CTS001	Cutis Laxa	65	0.710

50		MYL005	Myelofibrosis	71	0.602

51	P	MLN008	Melanoma	76	0.602