Search results for cer1

40 hits were found for cer1

#	Family	MCID	Name	MIFTS	Score
1		NRR002	Norrie Disease	59	13.113

2		CHR518	Chromosome 9p Deletion Syndrome	39	9.326

3	c	KLF004	Kleefstra Syndrome 1	53	9.144

4	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	1.780

5	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	1.780

6		SVR004	Severe Combined Immunodeficiency	70	1.761

7	P	OST002	Osteoporosis	76	1.297

8		CSY001	C Syndrome	61	1.215

9	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	1.215

10	P	CRN037	Craniosynostosis	67	1.215

11		SYN005	Synostosis	43	1.215

12		FGF014	Fgfr Craniosynostosis Syndromes	26	1.215

13	P	BRS047	Breast Cancer	97	0.753

14	P	PNC035	Pancreatic Cancer	87	0.753

15	P	OLG002	Oligodendroglioma	66	0.613

16	P	FBR017	Fibrosarcoma	55	0.603

17	P	ATS364	Autism	72	0.533

18	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.533

19	P	EPL164	Epilepsy	70	0.533

20		CHL098	Childhood Myocerebrohepatopathy Spectrum	21	0.514

21	P	TRT010	Teratoma	50	0.406

22	c	KNN009	Kenny-Caffey Syndrome, Type 1	35	0.364

23		EMB004	Embryonal Carcinoma	55	0.364

24	P	DRM053	Dermatitis, Atopic	65	0.257

25		IMM167	Immune Deficiency Disease	76	0.257

26		CMB007	Combined Immunodeficiency	56	0.257

27	P	CRN300	Coronary Heart Disease 1	73	0.182

28		ART140	Arteries, Anomalies of	52	0.182

29		LPP008	Lipoprotein Quantitative Trait Locus	65	0.182

30		TRG015	Trigonocephaly 2	25	0.182

31		NNL006	Non-Alcoholic Steatohepatitis	54	0.182

32		NNL005	Non-Alcoholic Fatty Liver Disease	63	0.182

33		CRN030	Coronary Stenosis	50	0.182

34		FTT001	Fatty Liver Disease	61	0.182

35		FRM011	Frem1 Autosomal Recessive Disorders	8	0.182

36		SFT003	Soft Tissue Sarcoma	43	0.182

37	c	RNG025	Ring Chromosome 9	19	0.182

38	P	HYP265	Hypotonia	42	0.182

39		ISL084	Isolated Trigonocephaly	26	0.182

40	P	RNG032	Ring Chromosome	39	0.182