Search results for camk2b

#	Family	MCID	Name	MIFTS	Score
1	c	INT562	Intellectual Developmental Disorder, Autosomal Dominant 54	27	39.762

2	c	CNG031	Congenital Nervous System Abnormality	32	18.288

3	P	NRV007	Nervous System Disease	67	18.288

4	P	MCR010	Microcephaly	59	14.108

5	P	ATS364	Autism	74	14.005

6	c	ATS007	Autism Spectrum Disorder	70	14.005

7	P	FRG001	Fragile X Syndrome	69	11.435

8	P	DYS154	Dystonia	66	9.730

9	c	ATS203	Autosomal Dominant Non-Syndromic Intellectual Disability	34	8.558

10	c	ANT085	Anterior Segment Dysgenesis 5	47	8.086

11	P	FCL005	Focal Segmental Glomerulosclerosis	59	8.086

12	c	INT561	Intellectual Developmental Disorder, Autosomal Dominant 53	26	1.527

13		CRB169	Cerebellar Atrophy, Developmental Delay, and Seizures	46	1.527

14		HYP265	Hypotonia	46	1.492

15		OTP003	Oto-Palatal-Digital Syndrome	36	1.382

16		HYP037	Hyperhomocysteinemia	51	1.284

17		RNL114	Renal Cell Carcinoma, Nonpapillary	80	1.161

18		RNL065	Renal Cell Carcinoma, Papillary, 1	79	1.161

19		CLL002	Collecting Duct Carcinoma	64	1.161

20	P	NRB001	Neuroblastoma	62	1.123

21	P	EPS003	Episodic Ataxia	60	1.080

22	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	66	1.028

23	P	SCL018	Scoliosis	56	1.028

24	P	EPL164	Epilepsy	71	1.028

25		MTR086	Motor Stereotypies	31	1.028