Search results for CNTN4

29 hits were found for CNTN4

#	Family	MCID	Name	MIFTS	Score
1	P	ATS364	Autism	70	3.923

2	c	ATS007	Autism Spectrum Disorder	67	3.341

3	P	SCH015	Schizophrenia	74	3.058

4		CHR667	Chromosome 3pter-P25 Deletion Syndrome	41	2.324

5	P	PRV006	Pervasive Developmental Disorder	57	2.162

6	c	SPN096	Spinocerebellar Ataxia 21	40	2.162

7	c	SPN290	Spinocerebellar Ataxia 15	40	2.162

8		CHR390	Chromosome 14q11-Q22 Deletion Syndrome	38	2.162

9	c	CFF011	Coffin-Siris Syndrome 6	35	2.162

10		CHR523	Chromosome 15q11.2 Deletion Syndrome	33	2.162

11	c	SPN098	Spinocerebellar Ataxia 25	29	2.162

12	c	CHR565	Chromosomal Deletion Syndrome	25	2.162

13		LPN002	Lip and Oral Cavity Cancer	19	0.115

14	P	NRB001	Neuroblastoma	72	0.081

15	c	PRM196	Premature Ovarian Failure 1	67	0.081

16		GT001	Gout	64	0.081

17		NPH091	Nephrolithiasis, Calcium Oxalate	60	0.081

18	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.081

19		ORL011	Oral Cancer	60	0.081

20		VSL002	Visual Epilepsy	59	0.081

21		THR024	Thrombosis	57	0.081

22	P	CRD246	Cardiovascular System Disease	57	0.081

23		NPH009	Nephrolithiasis	55	0.081

24		APR001	Apraxia	52	0.081

25		BKR002	Baker-Gordon Syndrome	49	0.081

26		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.081

27		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.081

28		CHR178	Chromosomal Triplication	35	0.081

29		CHR244	Chromosome 3p Duplication	14	0.081