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113 hits were found for 'alloimmunization'

#	++	Fam	MCID	Name	MIFTS	Score
1			FTL012	Fetal and Neonatal Alloimmune Thrombocytopenia	26	4.832
2		c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	14	4.581
3			NTR014	Neutropenia, Alloimmune Neonatal	9	4.119
4			THR095	Thrombocytopenia, Neonatal Alloimmune	13	3.709
5			THR094	Thrombocytopenia, Neonatal Alloimmune, Bak Antigen Related	3	3.239
6		c	MMB010	Membranous Congenital Glomerulonephritis Due to Anti-Maternal Neutral Endopeptidase Alloimmunization	1	3.239
7			ATM004	Autoimmune Thrombocytopenic Purpura	62	2.368
8		c	THR014	Thrombocytopenia	66	0.349
9			THR013	Thoracic Outlet Syndrome	53	0.206
10			SDR002	Siderosis	50	0.192
11			THR035	Thrombasthenia	49	0.192
12		c	NTR004	Neutropenia	59	0.160
13			SCK005	Sickle Cell Disease	58	0.160
14			DND005	Dandy-Walker Complex	22	0.160
15			PRP030	Purpura	60	0.151
16			VND002	Van Der Woude Syndrome	34	0.151
17			FCT013	Factor V Leiden Thrombophilia	31	0.151
18			NNT016	Neonatal Hemochromatosis	41	0.141
19			RPP001	Rapp-Hodgkin Syndrome	37	0.141
20			BLD122	Bleeding Disorder, Platelet-Type, 16, Autosomal Dominant	23	0.130
21			RPD005	Rapidly Involuting Congenital Hemangioma	19	0.130
22			ANK002	Ankylosing Spondylitis	75	0.119
23			HYD012	Hydrops Fetalis	61	0.119
24		P	CNG052	Congenital Amegakaryocytic Thrombocytopenia	45	0.119
25			HNM001	Hinman's Syndrome	28	0.119
26			TFT003	Tufting Enteropathy	26	0.119
27			ATX002	Ataxia Telangiectasia	81	0.106
28		P	HMC003	Hemochromatosis	73	0.106
29			SCK003	Sickle Cell Anemia	67	0.106
30		P	GRF002	Graft Versus Host Disease	64	0.106
31		c	ESS003	Essential Thrombocythemia	60	0.106
32			HML002	Hemolytic Anemia	60	0.106
33			GRY002	Gray Platelet Syndrome	51	0.106
34			LKM002	Leukemia	70	0.092
35			THL005	Thalassemia	69	0.092
36			GLN003	Glanzmann's Thrombasthenia	68	0.092
37		P	HMP004	Hemophilia B	66	0.092
38		P	LVR013	Liver Disease	62	0.092
39			THR004	Thrombocytosis	61	0.092
40		c	NPH012	Nephrotic Syndrome	57	0.092
41			HPR003	Heparin-Induced Thrombocytopenia	55	0.092
42		P	PNC001	Pancytopenia	55	0.092
43		P	CHR092	Chronic Myeloproliferative Disease	48	0.092
44		c	OPT004	Optic Atrophy	41	0.092
45		c	PRM041	Primary Cortisol Resistance	19	0.092
46			AND002	Androgen Insensitivity Syndrome	75	0.075
47			ACN002	Acanthosis Nigricans	70	0.075
48			ALP006	Alpha Thalassemia	68	0.075
49			WST001	West Syndrome	64	0.075
50		c	AXN002	Axenfeld-Rieger Syndrome	57	0.075
51			MYC002	Mycobacterium Avium Complex Disease	56	0.075
52			ATM010	Autoimmune Hemolytic Anemia	55	0.075
53		c	MYL014	Myeloproliferative Disorder	54	0.075
54			SPL018	Splenomegaly	50	0.075
55		c	CHR417	Chronic Graft Versus Host Disease	49	0.075
56		P	THR090	Thrombocythemia 1	48	0.075
57		c	PRN026	Porencephaly	40	0.075
58			OP3001	Opa3-Related 3-Methylglutaconic Aciduria	36	0.075
59			PMP002	Pemphigoid Gestationis	35	0.075
60		P	DRR003	Diarrhea 5, with Tufting Enteropathy, Congenital	23	0.075
61			FTL004	Fetal Erythroblastosis	19	0.075
62			RHM007	Rheumatic Congestive Heart Failure	19	0.075
63		c	KRN003	Kernicterus Due to Isoimmunization	18	0.075
64			PLY001	Polycythemia Vera	77	0.053
65			APL001	Aplastic Anemia	77	0.053
66			LVR012	Liver Cirrhosis	69	0.053
67		P	MYL005	Myelofibrosis	67	0.053
68		P	ANG001	Angelman Syndrome	67	0.053
69		P	HPT001	Hepatitis C	66	0.053
70		c	HPT021	Hepatitis	65	0.053
71			BLL006	Bullous Pemphigoid	65	0.053
72			ART019	Aortic Valve Stenosis	64	0.053
73		c	HMP007	Hemophilia	64	0.053
74			CHR012	Chronic Granulomatous Disease	63	0.053
75			BRN002	Bronchiolitis	60	0.053
76		P	GLM007	Glomerulonephritis	60	0.053
77		P	BRN012	Bronchiolitis Obliterans	58	0.053
78		c	HPT003	Hepatitis a	57	0.053
79			NSY001	N Syndrome	57	0.053
80		P	BRN019	Bernard-Soulier Syndrome	56	0.053
81			HPT022	Hepatoblastoma	56	0.053
82		c	EMR001	Emery-Dreifuss Muscular Dystrophy	56	0.053
83		c	ACT135	Acute Graft Versus Host Disease	55	0.053
84			VNW001	Von Willebrand's Disease	55	0.053
85			CHL068	Cholestasis	55	0.053
86		P	CNJ013	Conjunctivitis	55	0.053
87			THR009	Thrombocytopenia-Absent Radius Syndrome	55	0.053
88			THY033	Thyrotoxicosis	55	0.053
89			PLY018	Polycythemia	55	0.053
90			NPH051	Nephritis	55	0.053
91			ALL009	Allergic Conjunctivitis	55	0.053
92			HST011	Histoplasmosis	54	0.053
93			PRT018	Portal Vein Thrombosis	54	0.053
94			CHR285	Chronic Myelomonocytic Leukemia	53	0.053
95			CHR005	Chorioamnionitis	52	0.053
96		c	CNT035	Central Nervous System Disease	52	0.053
97			ART001	Arterial Tortuosity Syndrome	52	0.053
98			TCL004	T-Cell Leukemia	50	0.053
99		c	PRG060	Pregnancy Loss	48	0.053
100			HMT018	Hematopoietic Stem Cell Transplantation	41	0.053
101			GRN017	Granulocytopenia	41	0.053
102			AND003	Andersen-Tawil Syndrome	39	0.053
103			HRP002	Herpes Gestationis	37	0.053
104			HYD028	Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia	37	0.053
105			EMN001	Emanuel Syndrome	34	0.053
106		c	ATX010	Ataxia Neuropathy Spectrum	33	0.053
107			ADS002	Adie Syndrome	32	0.053
108			LKM004	Leukemia, B-Cell, Chronic	29	0.053
109		c	HMP017	Hemophilia a, Congenital	26	0.053
110			AND005	Androgen Insensitivity Syndrome, Mild	19	0.053
111			LKM005	Leukemia, T-Cell, Chronic	18	0.053
112		c	BNG076	Benign Exophthalmos Syndrome	17	0.053
113		P	ISC010	Isochromosome Yp	14	0.053

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The MalaCards human disease database
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Version 1.05.183 02 Mar 2014