Search results for [ge] HDAC8

#	Family	MCID	Name	MIFTS	Score
1	c	CRN209	Cornelia De Lange Syndrome 5	40	29.267

2	P	CRN015	Cornelia De Lange Syndrome	66	26.296

3	c	CRN139	Cornelia De Lange Syndrome 1	62	19.071

4		INT449	Intellectual Developmental Disorder, X-Linked, Syndromic, Wilson-Turner Type	49	15.601

5	P	MCR010	Microcephaly	59	15.601

6	P	FRN036	Frontonasal Dysplasia 1	55	10.218

7	P	RTT002	Rett Syndrome	78	10.218

8	P	ATR010	Atrial Heart Septal Defect	58	10.218

9	P	FNC044	Fanconi Anemia, Complementation Group C	56	7.225

10	P	SYN060	Syndactyly, Type Iii	44	7.225

11		RBR002	Roberts-Sc Phocomelia Syndrome	66	7.225

12		HYP748	Hypertelorism	50	7.225

13		KBG001	Kbg Syndrome	55	7.225

14		MTR088	Mature T-Cell and Nk-Cell Lymphoma	43	7.225

15		CHR593	Chromosome 16p13.3 Deletion Syndrome, Proximal	67	7.225

16		CRN320	Cornelia De Lange Syndrome 3 with or Without Midline Brain Defects	43	7.225

17	P	CRN321	Cornelia De Lange Syndrome 4 with or Without Midline Brain Defects	45	7.225

18		WHT019	White-Sutton Syndrome	46	7.225

19	c	CNG031	Congenital Nervous System Abnormality	32	7.225

20		FML286	Familial Isolated Trichomegaly	34	7.225

21		OPT062	Optic Atrophy 10 with or Without Ataxia, Mental Retardation, and Seizures	43	7.225

22		CHR515	Chronic Atrial and Intestinal Dysrhythmia	44	7.225

23	P	PLY014	Polycystic Kidney Disease	70	7.225

24		EYL005	Eyelid Disease	41	7.225

25		INT276	Interatrial Communication	51	7.225