Search results for serac1

#	Family	MCID	Name	MIFTS	Score
1		3MT013	3-Methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome	50	79.943

2		SRC031	Serac1 Deficiency	9	30.644

3	c	3MT007	3-Methylglutaconic Aciduria	36	19.407

4	P	DYS154	Dystonia	66	16.463

5	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	66	12.608

6		LGH007	Leigh Syndrome	69	11.773

7	P	CFF008	Coffin-Siris Syndrome 1	64	10.274

8	c	HRD010	Hereditary Spastic Paraplegia	68	9.998

9	P	MTC195	Mitochondrial Oxidative Phosphorylation Disorder	26	9.048

10	c	3MT019	3-Methylglutaconic Aciduria, Type Iv	34	9.004

11	P	MTC010	Mitochondrial Dna Depletion Syndrome	47	8.448

12	c	3MT015	3-Methylglutaconic Aciduria, Type I	47	8.337

13		BRT005	Barth Syndrome	57	7.690

14		SNG007	Sengers Syndrome	48	7.525

15	c	3MT014	3-Methylglutaconic Aciduria, Type V	49	7.477

16	c	MTC058	Mitochondrial Dna Depletion Syndrome 6	51	7.477

17		ORG002	Organic Acidemia	46	7.477

18	c	MTC056	Mitochondrial Dna Depletion Syndrome 4a	63	7.265

19	c	SPS071	Spastic Paraplegia 48, Autosomal Recessive	43	7.265

20		MHM001	Mehmo Syndrome	49	7.265

21	c	SPS148	Spastic Paraplegia 31, Autosomal Dominant	46	7.265

22		CHR568	Chromosome 6q24-Q25 Deletion Syndrome	37	7.265

23	c	TRC100	Trichothiodystrophy 3, Photosensitive	45	7.265

24		AMN002	Amino Acid Metabolic Disorder	44	7.265

25	P	SNS001	Sensorineural Hearing Loss	59	3.075