Search results for cer1

39 hits were found for cer1

#	Family	MCID	Name	MIFTS	Score
1		NRR002	Norrie Disease	61	13.648

2		CHR518	Chromosome 9p Deletion Syndrome	40	9.864

3	c	KLF004	Kleefstra Syndrome 1	50	9.135

4		SVR004	Severe Combined Immunodeficiency	72	4.499

5	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	3.511

6	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	3.511

7	P	OST002	Osteoporosis	76	2.638

8	P	FBR017	Fibrosarcoma	56	2.420

9		CSY001	C Syndrome	61	2.310

10	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	2.310

11		SYN005	Synostosis	43	2.310

12	P	CRN037	Craniosynostosis	68	2.310

13		FGF014	Fgfr Craniosynostosis Syndromes	25	2.310

14		CHL098	Childhood Myocerebrohepatopathy Spectrum	21	2.063

15	P	TRT010	Teratoma	51	1.631

16	c	KNN009	Kenny-Caffey Syndrome, Type 1	35	1.459

17		EMB004	Embryonal Carcinoma	56	1.459

18	P	DRM053	Dermatitis, Atopic	65	1.032

19		IMM167	Immune Deficiency Disease	78	1.032

20		CMB007	Combined Immunodeficiency	57	1.032

21	P	BRS047	Breast Cancer	98	0.753

22	P	PNC035	Pancreatic Cancer	86	0.753

23		ART140	Arteries, Anomalies of	53	0.730

24	P	CRN300	Coronary Heart Disease 1	73	0.730

25		LPP008	Lipoprotein Quantitative Trait Locus	65	0.730

26		NNL006	Non-Alcoholic Steatohepatitis	54	0.730

27		NNL005	Non-Alcoholic Fatty Liver Disease	63	0.730

28		TRG015	Trigonocephaly 2	25	0.730

29	P	RNG032	Ring Chromosome	39	0.730

30		CRN030	Coronary Stenosis	50	0.730

31		FTT001	Fatty Liver Disease	62	0.730

32		ISL084	Isolated Trigonocephaly	26	0.730

33		FRM011	Frem1 Autosomal Recessive Disorders	8	0.730

34	P	HYP265	Hypotonia	42	0.730

35	c	RNG025	Ring Chromosome 9	19	0.730

36	P	OLG002	Oligodendroglioma	66	0.614

37	P	ATS364	Autism	69	0.533

38	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.533

39	P	EPL164	Epilepsy	68	0.533