Search results for sec61a1

#	Family	MCID	Name	MIFTS	Score
1	c	TBL034	Tubulointerstitial Kidney Disease, Autosomal Dominant, 5	24	32.898

2	P	KDN018	Kidney Disease	75	15.483

3		PLY023	Polycystic Liver Disease	62	12.861

4		CYS001	Cystic Fibrosis	78	11.435

5		BRL010	Buruli Ulcer	47	9.250

6	c	ATS483	Autosomal Dominant Severe Congenital Neutropenia	33	8.457

7	P	TBL031	Tubulointerstitial Kidney Disease, Autosomal Dominant, 1	51	8.417

8	c	RTN144	Retinitis Pigmentosa 61	31	8.086

9		UTR037	Uterine Corpus Sarcoma	38	8.086

10	P	ZLL001	Zellweger Syndrome	64	8.086

11	P	CNT116	Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a	54	1.756

12		AGM019	Agammaglobulinemia, X-Linked	73	1.511

13	P	AGM001	Agammaglobulinemia	65	1.511

14	c	TBL032	Tubulointerstitial Kidney Disease, Autosomal Dominant, 2	45	1.308

15		CLN015	Colon Adenocarcinoma	55	1.308

16	P	NTR004	Neutropenia	61	1.197

17		PYR037	Pyruvate Carboxylase Deficiency	48	1.164

18		SKN016	Skin Disease	67	1.129

19		CLB003	Coloboma of Optic Nerve	54	1.090

20	P	ADN016	Adenocarcinoma	64	1.090

21		GLB002	Glioblastoma	67	1.090

22	P	NSP012	Nasopharyngeal Carcinoma	62	1.045

23		DFC004	Deficiency Anemia	74	0.992

24		17Q009	17q12 Recurrent Deletion Syndrome	19	0.992

25	c	PSR023	Psoriasis 1	55	0.924