Search results for cep63

#	Family	MCID	Name	MIFTS	Score
1	c	SCK032	Seckel Syndrome 6	30	37.981

2	c	PRM031	Primary Autosomal Recessive Microcephaly	51	18.233

3	c	MYP119	Myopathy, Myofibrillar, 7	35	16.209

4	P	MCR010	Microcephaly	59	15.909

5	P	SCK004	Seckel Syndrome	55	14.859

6	P	DYS005	Dyslexia	40	11.979

7	P	CNR004	Cone-Rod Dystrophy 2	78	10.819

8	c	PRM212	Primary Microcephaly	39	9.498

9		ISL014	Isolated Growth Hormone Deficiency, Type Ia	58	8.707

10	P	MCR258	Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii	56	8.633

11	c	HRD010	Hereditary Spastic Paraplegia	68	8.558

12	c	MCR239	Microcephaly 5, Primary, Autosomal Recessive	49	7.827

13	P	MRG008	Meier-Gorlin Syndrome 1	57	7.650

14	c	BRN140	Brain Small Vessel Disease 2	39	7.650

15	P	MSC022	Mosaic Variegated Aneuploidy Syndrome	52	7.650

16	c	CNG031	Congenital Nervous System Abnormality	32	7.650

17		RDN001	Reading Disorder	44	7.650

18	c	THY109	Thyroid Cancer, Nonmedullary, 1	57	2.024

19		THY029	Thyroid Carcinoma	52	2.024

20	P	BLD134	Bladder Cancer	74	1.671

21		PPL002	Papillary Carcinoma	45	1.491

22	P	NRB001	Neuroblastoma	62	1.274

23	P	MLN007	Male Infertility	59	1.202

24	P	INF032	Infertility	59	1.202

25		LRN003	Learning Disability	45	1.160