Search results for kirrel3

#	Family	MCID	Name	MIFTS	Score
1	P	ATS364	Autism	74	14.647

2	P	FCL005	Focal Segmental Glomerulosclerosis	59	12.074

3		JCB001	Jacobsen Syndrome	48	11.036

4	c	INT515	Intellectual Developmental Disorder, Autosomal Dominant 4	26	10.722

5	c	ATS203	Autosomal Dominant Non-Syndromic Intellectual Disability	34	9.475

6		HML046	Heimler Syndrome 2	33	8.538

7	c	FML015	Familial Nephrotic Syndrome	47	8.538

8	c	ATS007	Autism Spectrum Disorder	70	5.621

9		CRB169	Cerebellar Atrophy, Developmental Delay, and Seizures	46	3.802

10		ESP021	Esophageal Cancer	83	1.424

11		ESP027	Esophagus Squamous Cell Carcinoma	58	1.424

12		DND001	Dandy-Walker Syndrome	50	1.303

13	P	ATT013	Attention Deficit-Hyperactivity Disorder	66	1.303

14	P	CRB045	Cerebellar Hypoplasia	40	1.303

15	P	MCR010	Microcephaly	59	1.268

16	c	INT514	Intellectual Developmental Disorder, Autosomal Dominant 3	32	1.187

17	P	BRS047	Breast Cancer	97	0.712

18	P	GLM040	Glioma Susceptibility 1	71	0.630

19		NRF008	Neurofibromatosis-Noonan Syndrome	79	0.630

20	c	MSM022	Mismatch Repair Cancer Syndrome 1	73	0.630

21		MNN043	Meningioma, Familial	81	0.630

22	c	GLM025	Glioma Susceptibility 2	32	0.630

23	c	GLM047	Glioma Susceptibility 3	34	0.630

24	c	GLM043	Glioma Susceptibility 9	31	0.630

25	P	OLG002	Oligodendroglioma	66	0.630