MalaCards: Search human diseases

The MalaCard for "alloimmunization" has been retired.
Searching MalaCards for entries containing "alloimmunization"

72 hits were found for 'alloimmunization'

#	F	MCID	Name	MIFTS	Score
1		NNT014	Neonatal Alloimmune Thrombocytopenia	43.3	5.751
2		THR001	Thrombocytopenia Due to Platelet Alloimmunization	19.7	4.331
3		NTR020	Neutropenia, Neonatal Alloimmune	3.0	4.272
4		FTL012	Fetal and Neonatal Alloimmune Thrombocytopenia	8.0	3.654
5	P	THR014	Thrombocytopenia	78.7	0.242
6	c	THR037	Thrombocytopenia 2	24.9	0.185
7		NTR004	Neutropenia	78.3	0.131
8		AND005	Androgen Insensitivity Syndrome, Mild	16.3	0.117
9		GT1007	Gata1-related Thrombocytopenia with Beta-thalassemia	9.6	0.117
10		THR042	Thrombocytopenia, X-linked	23.3	0.117
11		CNG052	Congenital Amegakaryocytic Thrombocytopenia	44.1	0.101
12		CYC007	Cyclic Thrombocytopenia	39.5	0.101
13		EVN001	Evans' Syndrome	47.8	0.101
14		GT1006	Gata1-related Thrombocytopenia	13.4	0.101
15		PRS052	Paris-trousseau Thrombocytopenia	17.0	0.101
16		THR013	Thoracic Outlet Syndrome	33.0	0.101
17		THR038	Thrombocytopenia Cerebellar Hypoplasia Short Stature	7.3	0.101
18		THR040	Thrombocytopenia with Elevated Serum Iga and Renal Disease	6.3	0.101
19		THR041	Thrombocytopenia, Acquired Amegakaryocytic	16.0	0.101
20	c	THR048	Thrombocytopenia 4	12.6	0.101
21		THR051	Thrombocytopenia with Beta-thalassemia, X-linked	17.4	0.101
22		THR065	Thrombocytopenia, X-linked, Intermittent	18.7	0.101
23		AND002	Androgen Insensitivity Syndrome	65.7	0.083
24		ART001	Arterial Tortuosity Syndrome	41.1	0.083
25	P	AXN002	Axenfeld-rieger Syndrome	47.1	0.083
26		GRF002	Graft Versus Host Disease	74.8	0.083
27		IMM010	Immunodeficiency	88.7	0.083
28		KRN003	Kernicterus Due to Isoimmunization	16.5	0.083
29		MYC002	Mycobacterium Avium Complex Disease	54.9	0.083
30		NPH015	Nephropathy	77.0	0.083
31		PRP030	Purpura	76.6	0.083
32		SCK005	Sickle Cell Disease	74.2	0.083
33		TRC078	Trichohepatoenteric Syndrome 2	15.5	0.083
34		WST001	West Syndrome	44.8	0.083
35		ADS002	Adie Syndrome	29.8	0.059
36		AND003	Andersen-tawil Syndrome	32.2	0.059
37		ANG001	Angelman Syndrome	57.8	0.059
38		ANK002	Ankylosing Spondylitis	88.2	0.059
39		ANM004	Anemia	87.0	0.059
40		ART019	Aortic Valve Stenosis	64.8	0.059
41		ATX002	Ataxia Telangiectasia	82.4	0.059
42		BCK002	Beckwith-wiedemann Syndrome	56.7	0.059
43		CHR417	Chronic Graft Versus Host Disease	59.6	0.059
44		CWD001	Cowden Disease	67.3	0.059
45		CYC004	Cyclic Hematopoiesis	28.0	0.059
46		ELN001	Elane-related Neutropenia	18.6	0.059
47	P	FCT013	Factor V Leiden Thrombophilia	28.0	0.059
48		GT1005	Gata1-related Neutropenia	12.4	0.059
49	P	HMP007	Hemophilia	72.1	0.059
50		HMT003	Hematopoiesis	69.9	0.059
51		HYP141	Hyperphenylalaninemia	47.9	0.059
52		NPH051	Nephritis	68.6	0.059
53		NTR001	Neutral Lipid Storage Disease	37.0	0.059
54		NTR009	Neutropenia Lethal Congenital with Eosinophilia	14.4	0.059
55		NTR010	Neutropenia Monocytopenia Deafness	6.9	0.059
56		NTR013	Neutropenia, Nonimmune Chronic Idiopathic, of Adults	16.6	0.059
57	c	NTR015	Neutropenia, Severe Congenital, Autosomal Dominant 1	17.0	0.059
58		PRM041	Primary Cortisol Resistance	13.7	0.059
59		PRN023	Prion Disease	78.3	0.059
60		RCR005	Recurrent Fever Multi-gene Panels	19.1	0.059
61		RHM007	Rheumatic Congestive Heart Failure	16.6	0.059
62		RPP001	Rapp-hodgkin Syndrome	19.2	0.059
63		SPN210	Spontaneous Abortion	65.3	0.059
64		SVR003	Severe Congenital Neutropenia	67.7	0.059
65	P	SVR013	Severe Congenital Neutropenia Autosomal Recessive 3	20.5	0.059
66		SVR014	Severe Congenital Neutropenia X-linked	17.2	0.059
67	P	SVR026	Severe Congenital Neutropenia, Autosomal Dominant, 2	17.0	0.059
68	c	SVR027	Severe Congenital Neutropenia, Autosomal Recessive, 4	18.9	0.059
69	c	THL005	Thalassemia	75.8	0.059
70		TTN001	Tetanus Neonatorum	23.0	0.059
71	c	USH002	Usher Syndrome Type I	36.0	0.059
72	c	USH004	Usher Syndrome Type 2a	22.2	0.059