Search results for rab11a

#	Family	MCID	Name	MIFTS	Score
1		CYS001	Cystic Fibrosis	78	11.527

2	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	68	10.759

3	P	PRK057	Parkinson Disease, Late-Onset	81	10.690

4	P	CHR654	Charcot-Marie-Tooth Disease, Axonal, Type 2e	67	10.454

5	P	CHR071	Charcot-Marie-Tooth Disease	64	10.454

6	c	PNT034	Pontocerebellar Hypoplasia, Type 2e	53	10.454

7	c	ATS203	Autosomal Dominant Non-Syndromic Intellectual Disability	34	9.475

8		MCR094	Microvillus Inclusion Disease	54	9.070

9	c	AMY091	Amyotrophic Lateral Sclerosis 1	87	8.293

10	c	CNG478	Congenital Diarrhea	29	8.193

11	P	GRS003	Griscelli Syndrome	56	7.585

12	P	HRM001	Hermansky-Pudlak Syndrome	63	7.528

13	P	JBR020	Joubert Syndrome 1	72	7.392

14	P	CRP023	Carpenter Syndrome 1	57	7.392

15	P	CNR004	Cone-Rod Dystrophy 2	78	7.392

16	P	WRB002	Warburg Micro Syndrome 1	56	7.392

17	c	CHR516	Charcot-Marie-Tooth Disease, Type 4c	51	7.392

18	c	CHR646	Charcot-Marie-Tooth Disease, Axonal, Type 2b	51	7.392

19	P	RTN008	Retinitis Pigmentosa	80	7.392

20	c	HRD010	Hereditary Spastic Paraplegia	68	7.392

21	c	CNG031	Congenital Nervous System Abnormality	32	7.392

22		FND002	Fundus Dystrophy	55	7.392

23	P	INF038	Influenza	68	2.499

24	P	BRS047	Breast Cancer	97	2.201

25	P	PNC035	Pancreatic Cancer	91	1.798