Search results for OSM

65 hits were found for OSM

#	Family	MCID	Name	MIFTS	Score
1	c	OTS013	Otospondylomegaepiphyseal Dysplasia, Autosomal Recessive	57	8.860

2	P	OTS014	Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant	52	6.227

3	P	ART022	Arthritis	69	4.304

4	P	RHM011	Rheumatoid Arthritis	80	3.764

5		KPS004	Kaposi Sarcoma	75	3.728

6	P	PSR002	Psoriasis	62	3.728

7		PLS011	Plasmacytoma	56	3.728

8	c	BRS049	Breast Carcinoma in Situ	51	3.087

9	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	3.043

10	c	ART144	Arthrogryposis, Distal, Type 1a	61	3.043

11		NNT012	Neonatal Jaundice	53	3.043

12		CHR563	Chronic Eosinophilic Leukemia	48	3.043

13		OBS082	Obstructive Nephropathy	42	3.043

14		CRB036	Cerebral Meningioma	34	3.043

15		OST016	Osteochondrosis	53	2.152

16		SDK001	Sodoku Disease	40	2.152

17	P	LKM002	Leukemia	68	0.204

18	P	MLN008	Melanoma	69	0.180

19		SKN019	Skin Melanoma	68	0.136

20	c	BRN108	Branchiootic Syndrome 1	62	0.136

21		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.136

22	P	STC001	Stickler Syndrome	56	0.136

23	P	MLT020	Multiple Sclerosis	72	0.118

24		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.118

25		LNG099	Lung Disease	60	0.118

26		END081	Endosteal Hyperostosis, Autosomal Dominant	60	0.118

27	P	SNS001	Sensorineural Hearing Loss	60	0.118

28		LYM027	Lymphopenia	58	0.118

29		THR004	Thrombocytosis	51	0.118

30		MYL069	Myeloma, Multiple	85	0.096

31		OST012	Osteoarthritis	78	0.096

32		MRS002	Marshall Syndrome	58	0.096

33	P	INF037	Inflammatory Bowel Disease	54	0.096

34	P	INS002	in Situ Carcinoma	53	0.096

35		HLX001	Helix Syndrome	47	0.096

36	c	DFN137	Deafness, Autosomal Dominant 13	33	0.096

37	P	BRS047	Breast Cancer	97	0.068

38	c	SYS001	Systemic Lupus Erythematosus	86	0.068

39	P	GLM040	Glioma Susceptibility 1	81	0.068

40	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.068

41		AST005	Asthma	76	0.068

42		GLB015	Glioblastoma Multiforme	75	0.068

43	P	NRB001	Neuroblastoma	72	0.068

44	P	MYC007	Myocardial Infarction	70	0.068

45	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.068

46		CLF027	Cleft Palate, Isolated	64	0.068

47	P	GLM045	Glioma	63	0.068

48		TXC005	Toxic Shock Syndrome	62	0.068

49		LVR012	Liver Cirrhosis	62	0.068

50	P	LPS004	Lupus Erythematosus	61	0.068

51		DCT002	Ductal Carcinoma in Situ	59	0.068

52		ISC004	Ischemia	58	0.068

53		VGT001	Vogt-Koyanagi-Harada Disease	55	0.068

54	P	MYP006	Myopia	55	0.068

55		KNS001	Kniest Dysplasia	53	0.068

56	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.068

57		TCL027	T-Cell Acute Lymphoblastic Leukemia	51	0.068

58		HYP748	Hypertelorism	50	0.068

59		ATS010	Autosomal Recessive Disease	48	0.068

60		CHR074	Choriocarcinoma	47	0.068

61		GLL048	Glial Tumor	45	0.068

62		JNT004	Joint Laxity, Short Stature, and Myopia	45	0.068

63		DWR001	Dwarfism	44	0.068

64		PPL052	Papillomatosis, Confluent and Reticulated	33	0.068

65		MGP001	Megaepiphyseal Dwarfism	15	0.068