Search results for six3

76 hits were found for six3

#	Family	MCID	Name	MIFTS	Score
1	c	HLP024	Holoprosencephaly 2	49	5.509

2		SCH018	Schizencephaly	52	4.998

3	P	HLP001	Holoprosencephaly	67	4.846

4		MCR013	Microphthalmia	57	2.442

5		ANN002	Anencephaly	56	2.442

6	P	HYP083	Hypopituitarism	53	2.442

7	c	HLP023	Holoprosencephaly 1	53	2.442

8		SLT005	Solitary Median Maxillary Central Incisor	49	2.442

9		SML028	Semilobar Holoprosencephaly	44	2.442

10	c	HLP026	Holoprosencephaly 3	48	1.767

11		CLB026	Colobomatous Microphthalmia	47	1.767

12	c	HLP028	Holoprosencephaly 5	45	1.767

13		ALB014	Alobar Holoprosencephaly	42	1.767

14		ATL016	Atelencephaly	13	1.767

15		SPT006	Septooptic Dysplasia	64	1.727

16	P	ANR048	Aniridia 1	63	1.727

17		MCR173	Microform Holoprosencephaly	44	1.727

18		LBR025	Lobar Holoprosencephaly	43	1.727

19		MDL020	Midline Interhemispheric Variant of Holoprosencephaly	40	1.727

20		SPT016	Septopreoptic Holoprosencephaly	33	1.727

21	P	RTN008	Retinitis Pigmentosa	79	1.673

22		PLL001	Pallister-Hall Syndrome	64	1.673

23		PTS001	Patau Syndrome	55	1.673

24		CLB010	Coloboma of Macula	52	1.673

25		CLL036	Culler-Jones Syndrome	51	1.673

26	c	ORF040	Orofaciodigital Syndrome Viii	50	1.673

27	c	HLP025	Holoprosencephaly 9	50	1.673

28	c	HLP016	Holoprosencephaly 11	47	1.673

29	c	HLP029	Holoprosencephaly 4	44	1.673

30	P	ORF002	Orofacial Cleft	44	1.673

31		PHY002	Physical Disorder	42	1.673

32	c	HLP027	Holoprosencephaly 7	40	1.673

33		CRP003	Corpus Callosum Lipoma	34	1.673

34		IRS003	Iris Disease	29	1.673

35		ALT002	Aleutian Mink Disease	28	1.673

36		HLP004	Holoprosencephaly, Recurrent Infections, and Monocytosis	28	1.673

37		CRB034	Cerebral Hemisphere Lipoma	26	1.673

38	c	CNG031	Congenital Nervous System Abnormality	24	1.673

39		CNT024	Central Nervous System Lipoma	21	1.673

40		GLB015	Glioblastoma Multiforme	75	0.091

41	P	INF032	Infertility	57	0.091

42	P	CHN012	Chondrosarcoma	56	0.091

43		HLX001	Helix Syndrome	47	0.091

44		CHN056	Chondrosarcoma, Extraskeletal Myxoid	46	0.091

45	P	EXT030	Extraosseous Chondrosarcoma	35	0.091

46	P	MYX008	Myxoid Chondrosarcoma	32	0.091

47	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.064

48	P	LNG064	Lung Cancer Susceptibility 3	78	0.064

49	P	LYN001	Lynch Syndrome	77	0.064

50		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.064

51	P	ADN016	Adenocarcinoma	64	0.064

52	P	GLM045	Glioma	63	0.064

53	P	KLL001	Kallmann Syndrome	61	0.064

54	P	MCR010	Microcephaly	59	0.064

55		EYD002	Eye Disease	58	0.064

56		LNG108	Langerhans Cell Histiocytosis	58	0.064

57		OPT070	Optic Nerve Hypoplasia, Bilateral	56	0.064

58	P	MRG008	Meier-Gorlin Syndrome 1	55	0.064

59	P	MLN007	Male Infertility	55	0.064

60		BRN015	Bronchiolo-Alveolar Adenocarcinoma	54	0.064

61		CLF001	Cleft Lip	53	0.064

62		FRY006	Fryns Microphthalmia Syndrome	52	0.064

63	P	AST007	Astrocytoma	51	0.064

64		HST010	Histiocytosis	48	0.064

65	c	SPL067	Split-Hand/foot Malformation 1	46	0.064

66		GLL048	Glial Tumor	45	0.064

67		ISL121	Isolated Split Hand-Split Foot Malformation	45	0.064

68		HRT030	Hartsfield Syndrome	44	0.064

69		DWR001	Dwarfism	44	0.064

70	c	RTN041	Retinitis Pigmentosa 11	42	0.064

71		ISL109	Isolated Cleft Lip	38	0.064

72		FML292	Familial Drusen	32	0.064

73		ISL011	Isolated Aniridia	31	0.064

74	c	CNG608	Congenital Hypopituitarism	30	0.064

75	c	MRG014	Meier-Gorlin Syndrome 6	25	0.064

76		RRS010	Rare Soft Tissue Tumor	18	0.064