Search results for gnb1

#	Family	MCID	Name	MIFTS	Score
1	c	INT453	Intellectual Developmental Disorder, Autosomal Dominant 42	36	45.048

2		HYP265	Hypotonia	46	30.498

3		GNB001	Gnb1 Encephalopathy	7	24.951

4		MYL009	Myelodysplastic Syndrome	64	24.175

5	P	DYS154	Dystonia	66	23.407

6	P	LKM062	Leukemia, Acute Lymphoblastic	69	19.775

7	P	STR020	Strabismus	57	19.343

8		CRB037	Cerebral Palsy	66	17.853

9	P	RTN008	Retinitis Pigmentosa	80	14.425

10	c	ATS007	Autism Spectrum Disorder	70	13.291

11	P	MCR010	Microcephaly	59	12.455

12		CRB159	Cerebral Visual Impairment	44	10.820

13		CLF027	Cleft Palate, Isolated	63	9.950

14		WST001	West Syndrome	64	9.433

15	P	HYP086	Hypothyroidism	68	9.260

16		CHR222	Chromosome 1p36 Deletion Syndrome	48	8.167

17	P	CNR004	Cone-Rod Dystrophy 2	78	7.976

18	c	OPT060	Optic Atrophy 8	25	7.650

19	c	NGH024	Night Blindness, Congenital Stationary, Type 1h	34	7.650

20	c	CHR035	Chronic Dacryoadenitis	16	7.650

21	P	ENC018	Encephalopathy	64	2.911

22		MST024	Mastocytosis, Cutaneous	65	2.730

23	P	MST009	Mastocytosis	66	2.730

24		SGC002	Sgce Myoclonus-Dystonia	23	2.049

25		VSL002	Visual Epilepsy	47	2.034