Search results for nog

60 hits were found for nog

#	Family	MCID	Name	MIFTS	Score
1		TRS002	Tarsal-Carpal Coalition Syndrome	36	13.666

2	P	PRX021	Proximal Symphalangism	49	5.665

3	c	MLT059	Multiple Synostoses Syndrome 1	30	5.406

4	c	BRC052	Brachydactyly, Type B2	44	5.356

5	c	SYM022	Symphalangism, Proximal, 1a	28	5.252

6	P	MLT072	Multiple Synostoses Syndrome	45	4.705

7		STP011	Stapes Ankylosis with Broad Thumbs and Toes	40	4.685

8		ANK001	Ankylosis	56	4.105

9	P	BRC006	Brachydactyly	50	3.955

10		SYN005	Synostosis	51	3.600

11		FBR011	Fibrodysplasia Ossificans Progressiva	65	3.570

12		ESP020	Esophageal Atresia	53	3.570

13	P	OTS001	Otosclerosis	53	3.570

14	P	CRN037	Craniosynostosis	66	3.538

15		NRL016	Neural Tube Defects	79	3.101

16	P	OST002	Osteoporosis	74	3.101

17	c	BRC051	Brachydactyly, Type B1	54	3.101

18		TRC040	Tracheoesophageal Fistula	48	3.101

19	P	SCL048	Sclerosteosis	48	3.064

20	P	HLP001	Holoprosencephaly	65	2.545

21		CHR619	Chromosome 2q35 Duplication Syndrome	60	2.545

22		SPN060	Spondylocarpotarsal Synostosis Syndrome	59	2.501

23		OSS012	Osseous Heteroplasia, Progressive	58	2.501

24		SYN031	Synovial Chondromatosis	48	2.501

25	c	BRC079	Brachydactyly, Type A2	46	2.501

26	c	BRC081	Brachydactyly, Type C	45	2.501

27		FBL002	Fibular Hypoplasia and Complex Brachydactyly	42	2.501

28		SYN086	Synostoses, Tarsal, Carpal, and Digital	37	2.501

29		FRS019	Farsightedness	36	2.501

30		ABR009	Abruzzo-Erickson Syndrome	33	2.501

31		HMR015	Humeroradial Synostosis	28	2.501

32		CHM005	Chemical Colitis	23	2.501

33		BND014	Bone Development Disease	30	1.769

34		MLN008	Melanoma	63	0.120

35	P	PNC035	Pancreatic Cancer	82	0.098

36	c	ACT134	Acute Liver Failure	53	0.098

37	c	INF145	Infantile Liver Failure Syndrome 1	47	0.098

38	P	BRS047	Breast Cancer	100	0.069

39		MYL069	Myeloma, Multiple	85	0.069

40	c	LKM061	Leukemia, Acute Myeloid	81	0.069

41	P	LKM002	Leukemia	72	0.069

42	P	GRF003	Graft-Versus-Host Disease	71	0.069

43		MYL005	Myelofibrosis	69	0.069

44	c	PRM196	Premature Ovarian Failure 1	68	0.069

45	P	MYL006	Myeloid Leukemia	67	0.069

46		CLF027	Cleft Palate, Isolated	64	0.069

47		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	62	0.069

48	P	CTR002	Cataract	59	0.069

49	P	PLY006	Polydactyly	57	0.069

50	P	RHB003	Rhabdomyosarcoma	57	0.069

51		CLF001	Cleft Lip	56	0.069

52		END081	Endosteal Hyperostosis, Autosomal Dominant	56	0.069

53		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	55	0.069

54		BLR001	Biliary Atresia	55	0.069

55	c	HMN021	Human T-Cell Leukemia Virus Type 1	53	0.069

56	P	PLY147	Polydactyly, Postaxial, Type A1	48	0.069

57		NRL018	Neural Tube Defects, Folate-Sensitive	47	0.069

58		TRC109	Tracheoesophageal Fistula with or Without Esophageal Atresia	46	0.069

59	c	CHR020	Chronic Interstitial Cystitis	39	0.069

60		HPT070	Hepatosplenic T-Cell Lymphoma	35	0.069