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86 hits were found for 'alloimmunization'

#		Family	MCID	Name	MIFTS	Score
1			FTL012	Fetal and Neonatal Alloimmune Thrombocytopenia	32	4.783
2		c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	20	4.624
3			NTR014	Neutropenia, Alloimmune Neonatal	7	3.981
4			THR095	Thrombocytopenia, Neonatal Alloimmune	8	3.453
5			THR094	Thrombocytopenia, Neonatal Alloimmune, Bak Antigen Related	5	3.250
6		c	MMB010	Membranous Congenital Glomerulonephritis Due to Anti-Maternal Neutral Endopeptidase Alloimmunization	3	3.250
7			ATM004	Autoimmune Thrombocytopenic Purpura	68	2.383
8		c	THR014	Thrombocytopenia	67	0.376
9			THR013	Thoracic Outlet Syndrome	54	0.201
10			SCK005	Sickle Cell Disease	62	0.174
11			PRP030	Purpura	67	0.164
12		c	NTR004	Neutropenia	65	0.164
13			FCT013	Factor V Leiden Thrombophilia	35	0.164
14			NNT016	Neonatal Hemochromatosis	44	0.153
15			RPP001	Rapp-Hodgkin Syndrome	34	0.153
16			ANK002	Ankylosing Spondylitis	75	0.130
17		P	CNG052	Congenital Amegakaryocytic Thrombocytopenia	45	0.130
18		P	ATX002	Ataxia Telangiectasia	93	0.116
19		P	HMC003	Hemochromatosis	80	0.116
20			SCK003	Sickle Cell Anemia	73	0.116
21		P	HML002	Hemolytic Anemia	68	0.116
22		P	GRF002	Graft Versus Host Disease	65	0.116
23			GRY002	Gray Platelet Syndrome	51	0.116
24		c	ESS003	Essential Thrombocythemia	50	0.116
25			HNM002	Hinman Syndrome	24	0.116
26		P	HMP004	Hemophilia B	80	0.100
27		P	LKM002	Leukemia	79	0.100
28		P	LVR013	Liver Disease	70	0.100
29		c	THL005	Thalassemia	68	0.100
30		c	NPH012	Nephrotic Syndrome	66	0.100
31			THR004	Thrombocytosis	63	0.100
32		P	PNC001	Pancytopenia	55	0.100
33		P	CHR092	Chronic Myeloproliferative Disease	55	0.100
34			EVN001	Evans' Syndrome	54	0.100
35			HPR003	Heparin-Induced Thrombocytopenia	45	0.100
36			SYN053	Syndromic Diarrhea	42	0.100
37			AND002	Androgen Insensitivity Syndrome	88	0.082
38		P	ALP006	Alpha Thalassemia	75	0.082
39			WST001	West Syndrome	64	0.082
40		c	AXN002	Axenfeld-Rieger Syndrome	60	0.082
41		c	ATM010	Autoimmune Hemolytic Anemia	57	0.082
42			MYC002	Mycobacterium Avium Complex Disease	57	0.082
43		P	THR090	Thrombocythemia 1	54	0.082
44			SDR002	Siderosis	53	0.082
45		P	HYP141	Hyperphenylalaninemia	49	0.082
46		c	MYL014	Myeloproliferative Disorder	39	0.082
47			SPL018	Splenomegaly	37	0.082
48		P	KRN003	Kernicterus Due to Isoimmunization	21	0.082
49			RHM007	Rheumatic Congestive Heart Failure	21	0.082
50			FTL004	Fetal Erythroblastosis	20	0.082
51		P	APL001	Aplastic Anemia	83	0.058
52			PLY001	Polycythemia Vera	83	0.058
53			GLN003	Glanzmann's Thrombasthenia	80	0.058
54			LVR012	Liver Cirrhosis	75	0.058
55		P	MYL005	Myelofibrosis	75	0.058
56		c	HPT021	Hepatitis	75	0.058
57			VNW001	Von Willebrand's Disease	74	0.058
58			CHR012	Chronic Granulomatous Disease	72	0.058
59		P	ANG001	Angelman Syndrome	70	0.058
60			ART019	Aortic Valve Stenosis	68	0.058
61		c	HMP007	Hemophilia	68	0.058
62		P	GLM007	Glomerulonephritis	66	0.058
63			HST011	Histoplasmosis	65	0.058
64			HPT022	Hepatoblastoma	65	0.058
65			CHL068	Cholestasis	63	0.058
66			ART001	Arterial Tortuosity Syndrome	62	0.058
67		c	PLY018	Polycythemia	61	0.058
68		P	CNJ013	Conjunctivitis	61	0.058
69			BRN002	Bronchiolitis	61	0.058
70			THR009	Thrombocytopenia-Absent Radius Syndrome	60	0.058
71		c	HPT003	Hepatitis a	60	0.058
72			BRN012	Bronchiolitis Obliterans	59	0.058
73		P	BRN019	Bernard-Soulier Syndrome	59	0.058
74			ALL009	Allergic Conjunctivitis	59	0.058
75			THY033	Thyrotoxicosis	58	0.058
76			PRT018	Portal Vein Thrombosis	57	0.058
77			CHR005	Chorioamnionitis	56	0.058
78		c	ART084	Arteriovenous Fistula	47	0.058
79		c	OPT004	Optic Atrophy	46	0.058
80			HYD028	Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia	43	0.058
81			AND003	Andersen-Tawil Syndrome	43	0.058
82			ADS002	Adie Syndrome	33	0.058
83		c	HMP017	Hemophilia a, Congenital	21	0.058
84		c	BNG076	Benign Exophthalmos Syndrome	21	0.058
85			AND005	Androgen Insensitivity Syndrome, Mild	18	0.058
86			TRN013	Transient Neonatal Thrombocytopenia	9	0.058

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Version 1.05.265 18 May 2014