Search results for "alloimmunization"

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

95 hits were found for 'alloimmunization'

#	Family	MCID	Name	MIFTS	Score
1		FTL012	Fetal and Neonatal Alloimmune Thrombocytopenia	34	4.781

2	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	21	4.600

3		CNG407	Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization	8	4.600

4		NTR014	Neutropenia, Alloimmune Neonatal	8	3.984

5		HML043	Hemolytic Disease of the Newborn with Kell Alloimmunization	4	3.984

6		THR095	Thrombocytopenia, Neonatal Alloimmune	8	3.370

7		THR094	Thrombocytopenia, Neonatal Alloimmune, Bak Antigen Related	5	3.253

8	c	THR014	Thrombocytopenia	69	0.378

9	c	NTR004	Neutropenia	65	0.218

10	c	NNT047	Neonatal Neutropenia	28	0.195

11		SCK005	Sickle Cell Disease	61	0.169

12		NNT016	Neonatal Hemochromatosis	49	0.149

13		PRP030	Purpura	65	0.138

14	c	HML002	Hemolytic Anemia	65	0.126

15		HYD012	Hydrops Fetalis	61	0.126

16	P	HMC003	Hemochromatosis	85	0.113

17		SCK003	Sickle Cell Anemia	84	0.113

18	c	THL005	Thalassemia	71	0.113

19	P	LVR013	Liver Disease	68	0.113

20	P	GRF002	Graft Versus Host Disease	64	0.113

21		THR013	Thoracic Outlet Syndrome	52	0.113

22		PYR007	Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia	43	0.113

23	P	ATM010	Autoimmune Hemolytic Anemia	66	0.098

24		END072	Endotheliitis	50	0.098

25		THR035	Thrombasthenia	44	0.098

26		SYN053	Syndromic Diarrhea	34	0.098

27		AND002	Androgen Insensitivity Syndrome	80	0.080

28	P	LKM002	Leukemia	76	0.080

29	P	ALP006	Alpha Thalassemia	74	0.080

30	c	AXN002	Axenfeld-Rieger Syndrome	69	0.080

31	P	SDR002	Siderosis	57	0.080

32	P	PNC001	Pancytopenia	48	0.080

33	c	PRN026	Porencephaly	47	0.080

34	c	CHR417	Chronic Graft Versus Host Disease	42	0.080

35		HMT018	Hematopoietic Stem Cell Transplantation	40	0.080

36		FTL004	Fetal Erythroblastosis	19	0.080

37	P	ATX002	Ataxia Telangiectasia	87	0.056

38		PLY001	Polycythemia Vera	85	0.056

39	P	APL001	Aplastic Anemia	84	0.056

40	c	BTT002	Beta Thalassemia	82	0.056

41		MYL040	Myelodysplastic Syndromes	79	0.056

42		GLN003	Glanzmann's Thrombasthenia	76	0.056

43		LVR012	Liver Cirrhosis	76	0.056

44		ANK002	Ankylosing Spondylitis	76	0.056

45		CHR012	Chronic Granulomatous Disease	74	0.056

46	P	MYL005	Myelofibrosis	74	0.056

47		HST011	Histoplasmosis	73	0.056

48	c	PRM002	Primary Hyperoxaluria	73	0.056

49	P	ANG001	Angelman Syndrome	71	0.056

50		ATM004	Autoimmune Thrombocytopenic Purpura	69	0.056

51		ART021	Arteriosclerosis	67	0.056

52	c	NPH012	Nephrotic Syndrome	67	0.056

53	c	HMP007	Hemophilia	64	0.056

54	P	BRN019	Bernard-Soulier Syndrome	64	0.056

55		ART019	Aortic Valve Stenosis	63	0.056

56	c	HPT021	Hepatitis	63	0.056

57		GRY002	Gray Platelet Syndrome	63	0.056

58	P	CNJ013	Conjunctivitis	61	0.056

59	c	ESS003	Essential Thrombocythemia	61	0.056

60		THR004	Thrombocytosis	60	0.056

61		BRN002	Bronchiolitis	60	0.056

62		BRN012	Bronchiolitis Obliterans	59	0.056

63	c	PLY018	Polycythemia	59	0.056

64	P	THR090	Thrombocythemia 1	58	0.056

65		CHL068	Cholestasis	58	0.056

66		MYC002	Mycobacterium Avium Complex Disease	58	0.056

67		THY033	Thyrotoxicosis	57	0.056

68	P	CNG052	Congenital Amegakaryocytic Thrombocytopenia	56	0.056

69		ART001	Arterial Tortuosity Syndrome	55	0.056

70		VND002	Van Der Woude Syndrome	55	0.056

71	c	CHR285	Chronic Myelomonocytic Leukemia	55	0.056

72		NPH051	Nephritis	53	0.056

73		AND003	Andersen-Tawil Syndrome	53	0.056

74		MMB002	Membranous Glomerulonephritis	52	0.056

75		HVD003	Hiv/aids	51	0.056

76		RPP001	Rapp-Hodgkin Syndrome	50	0.056

77		CHR005	Chorioamnionitis	50	0.056

78	P	CHR092	Chronic Myeloproliferative Disease	49	0.056

79	c	OPT004	Optic Atrophy	49	0.056

80		ALL009	Allergic Conjunctivitis	47	0.056

81		PRG060	Pregnancy Loss	47	0.056

82		GRN017	Granulocytopenia	46	0.056

83	P	ART084	Arteriovenous Fistula	46	0.056

84		SPL018	Splenomegaly	46	0.056

85		PMP002	Pemphigoid Gestationis	41	0.056

86		ADS002	Adie Syndrome	35	0.056

87		FCT013	Factor V Leiden Thrombophilia	34	0.056

88		DRR003	Diarrhea 5, with Tufting Enteropathy, Congenital	29	0.056

89		HNM002	Hinman Syndrome	28	0.056

90		TFT003	Tufting Enteropathy	28	0.056

91	c	BNG076	Benign Exophthalmos Syndrome	22	0.056

92		RHM007	Rheumatic Congestive Heart Failure	21	0.056

93		AND005	Androgen Insensitivity Syndrome, Mild	21	0.056

94		HRD137	Hereditary Isolated Aplastic Anemia	20	0.056

95		TRN013	Transient Neonatal Thrombocytopenia	7	0.056