Search results for mtm1

#	Family	MCID	Name	MIFTS	Score
1		MYP136	Myopathy, Centronuclear, X-Linked	62	98.986

2	P	MYP004	Myopathy	67	35.434

3	P	CNT004	Centronuclear Myopathy	54	32.021

4		PLY012	Polyhydramnios	47	17.714

5		RSP006	Respiratory System Disease	52	15.474

6		BTT016	Batten-Turner Congenital Myopathy	59	13.037

7	c	MYP123	Myopathy, Centronuclear, 1	53	12.508

8		NRM005	Neuromuscular Disease	63	12.368

9	P	CHR071	Charcot-Marie-Tooth Disease	64	12.166

10	P	PTS002	Ptosis	53	11.469

11		HYP265	Hypotonia	46	11.286

12	P	LMB006	Limb-Girdle Muscular Dystrophy	56	10.788

13	P	MSC003	Muscular Atrophy	55	10.442

14		TTH006	Tooth Disease	47	9.955

15	c	CHR521	Charcot-Marie-Tooth Disease, Type 4b1	47	9.939

16	c	PRM212	Primary Microcephaly	39	9.704

17	P	MYT021	Myotonic Dystrophy 1	74	9.697

18		MYT025	Myotubular Myopathy with Abnormal Genital Development	22	9.597

19	P	DST002	Distal Arthrogryposis	61	9.567

20		SNS003	Sensory Peripheral Neuropathy	51	9.567

21	c	AMY091	Amyotrophic Lateral Sclerosis 1	87	9.464

22	P	CHR654	Charcot-Marie-Tooth Disease, Axonal, Type 2e	67	9.464

23	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	73	9.322

24		MSC190	Muscular Disease	35	8.057

25	P	PRP019	Peripheral Nervous System Disease	63	7.781