Search results for "alloimmunization"

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

180 hits were found for 'alloimmunization'

#	Family	MCID	Name	MIFTS	Score
1		FTL012	Fetal and Neonatal Alloimmune Thrombocytopenia	32	4.344

2		THR095	Thrombocytopenia, Neonatal Alloimmune	13	4.040

3	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	42	4.023

4	c	CNG407	Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization	9	3.986

5		NTR014	Neutropenia, Alloimmune Neonatal	7	3.986

6		HML043	Hemolytic Disease of the Newborn with Kell Alloimmunization	4	3.270

7		THR100	Thrombocytopenic Purpura, Autoimmune	54	2.312

8	P	THR014	Thrombocytopenia	64	0.392

9	P	NTR004	Neutropenia	59	0.176

10		SCK005	Sickle Cell Disease	51	0.151

11	P	THL005	Thalassemia	64	0.144

12	P	HMC003	Hemochromatosis	72	0.111

13	P	HML002	Hemolytic Anemia	62	0.111

14		PRP030	Purpura	58	0.111

15		HYD012	Hydrops Fetalis	43	0.111

16	P	LVR013	Liver Disease	75	0.102

17		SCK003	Sickle Cell Anemia	71	0.091

18	P	MMB011	Membranous Nephropathy	54	0.091

19		THL018	Thalassemia Major	48	0.091

20		HMC038	Hemochromatosis, Neonatal	29	0.091

21	c	ATM010	Autoimmune Hemolytic Anemia	61	0.079

22	P	AXN010	Axenfeld-Rieger Syndrome, Type 3	55	0.079

23		BLD053	Blood Platelet Disease	46	0.079

24		CCN007	Cocoon Syndrome	45	0.079

25		END072	Endotheliitis	42	0.079

26		TNP003	Tn Polyagglutination Syndrome, Somatic	41	0.079

27		THR035	Thrombasthenia	39	0.079

28		ALR002	Al-Raqad Syndrome	36	0.079

29		FTL004	Fetal Erythroblastosis	33	0.079

30		DFC004	Deficiency Anemia	64	0.064

31		GLN010	Glanzmann Thrombasthenia	63	0.064

32	P	GLM007	Glomerulonephritis	59	0.064

33	P	PNC001	Pancytopenia	52	0.064

34	c	CHR417	Chronic Graft Versus Host Disease	51	0.064

35		THR013	Thoracic Outlet Syndrome	50	0.064

36	P	PRN026	Porencephaly	48	0.064

37		ACR041	Acromelic Frontonasal Dysostosis	45	0.064

38	P	SDR002	Siderosis	44	0.064

39		BRT030	Birth Defects	43	0.064

40		HMT018	Hematopoietic Stem Cell Transplantation	41	0.064

41	c	PRM225	Primary Thrombocytopenia	39	0.064

42	c	THR037	Thrombocytopenia 2	35	0.064

43		NNT011	Neonatal Anemia	33	0.064

44		PLC008	Placenta Disease	33	0.064

45		BLD052	Blood Group Incompatibility	27	0.064

46	P	APL001	Aplastic Anemia	75	0.046

47	c	LKM061	Leukemia, Acute Myeloid	73	0.046

48		MYL009	Myelodysplastic Syndrome	73	0.046

49	P	LKM002	Leukemia	71	0.046

50	P	HPT021	Hepatitis	69	0.046

51	P	DRV001	Dravet Syndrome	69	0.046

52		LVR012	Liver Cirrhosis	67	0.046

53	P	KDN018	Kidney Disease	66	0.046

54	P	EPL164	Epilepsy	66	0.046

55	P	MYL006	Myeloid Leukemia	66	0.046

56		CHR012	Chronic Granulomatous Disease	65	0.046

57	P	CNJ013	Conjunctivitis	64	0.046

58		HMT002	Hematologic Cancer	64	0.046

59	c	HMP029	Hemophilia a	63	0.046

60		HYP066	Hyperglycemia	61	0.046

61	c	ACT073	Acute Leukemia	60	0.046

62	P	ENC018	Encephalopathy	59	0.046

63		STT001	Status Epilepticus	59	0.046

64		CHL068	Cholestasis	59	0.046

65		ART021	Arteriosclerosis	58	0.046

66		BRN012	Bronchiolitis Obliterans	58	0.046

67	P	HMP007	Hemophilia	57	0.046

68		GST033	Gestational Diabetes	57	0.046

69	c	PRC016	Pre-Eclampsia	56	0.046

70		BRN002	Bronchiolitis	56	0.046

71		CHR285	Chronic Myelomonocytic Leukemia	56	0.046

72		MCS002	Mucositis	55	0.046

73		ESP023	Esophageal Disease	54	0.046

74	P	ECL001	Eclampsia	54	0.046

75		THL016	Thalassemias, Alpha-	53	0.046

76		HMG005	Hemoglobinopathy	52	0.046

77		HST011	Histoplasmosis	52	0.046

78	P	PRC031	Preeclampsia/eclampsia 1	51	0.046

79		ALL009	Allergic Conjunctivitis	51	0.046

80	P	RNL028	Renal Tubular Dysgenesis	51	0.046

81		VND002	Van Der Woude Syndrome	50	0.046

82		NNT012	Neonatal Jaundice	50	0.046

83		HPT074	Hepatic Adenoma, Somatic	50	0.046

84	c	INH020	Inherited Metabolic Disorder	49	0.046

85		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	48	0.046

86		RPP001	Rapp-Hodgkin Syndrome	48	0.046

87		CHR005	Chorioamnionitis	48	0.046

88	P	TRC086	Trichohepatoenteric Syndrome 1	48	0.046

89	c	HMG001	Hemoglobin C Disease	47	0.046

90		HMS001	Hemosiderosis	46	0.046

91		HRT007	Heart Cancer	46	0.046

92		HST017	Histiocytosis-Lymphadenopathy Plus Syndrome	46	0.046

93	P	INF016	Infantile Epileptic Encephalopathy	46	0.046

94		INC022	Inclusion-Cell Disease	46	0.046

95	P	KRN004	Kernicterus	46	0.046

96		GRN017	Granulocytopenia	44	0.046

97	c	HMG003	Hemoglobin E Disease	44	0.046

98		ECT093	Ectopic Cushing Syndrome	43	0.046

99		DRR008	Diarrhea 1, Secretory Chloride, Congenital	42	0.046

100		BLR008	Bilirubin Metabolic Disorder	42	0.046

101	c	CHR064	Chronic Monocytic Leukemia	42	0.046

102		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	41	0.046

103		SPR007	Superior Mesenteric Artery Syndrome	41	0.046

104		IRN002	Iron Metabolism Disease	41	0.046

105		ESP025	Esophagus Adenocarcinoma	41	0.046

106		ESN004	Eosinophilic Gastritis	41	0.046

107		THL017	Thalassemia Intermedia	40	0.046

108	c	SCN005	Secondary Hypertrophic Osteoarthropathy	40	0.046

109		EXN001	Exanthema Subitum	39	0.046

110	c	HMC010	Hemochromatosis, Type 3	39	0.046

111		TTZ003	Tietz Albinism-Deafness Syndrome	39	0.046

112	c	EPL029	Epileptic Encephalopathy, Early Infantile, 9	39	0.046

113		MYH012	Myhre Syndrome	38	0.046

114		BLD054	Blood Protein Disease	37	0.046

115		SHW001	Shwartzman Phenomenon	37	0.046

116		MYP100	Myopathy, X-Linked, with Excessive Autophagy	37	0.046

117		BNS002	Bone Structure Disease	37	0.046

118		CPL005	Capillary Disease	36	0.046

119		IMM003	Immunoglobulin Alpha Deficiency	36	0.046

120		KLN009	Kleine-Levin Hibernation Syndrome	36	0.046

121		NTR005	Nutritional Deficiency Disease	36	0.046

122		PRC005	Pericardial Tuberculosis	36	0.046

123		MTL002	Metal Metabolism Disorder	35	0.046

124		ATM012	Autoimmune Disease of Blood	35	0.046

125		PMP002	Pemphigoid Gestationis	35	0.046

126		ADP007	Adie Pupil	34	0.046

127		PNC028	Pancreatic Steatorrhea	34	0.046

128		PLY131	Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes	34	0.046

129		CNG436	Congenital Disorder of Deglycosylation	34	0.046

130		RMN001	Rumination Disorder	34	0.046

131		LRY017	Laryngeal Disease	34	0.046

132	P	TST001	Testicular Leydig Cell Tumor	33	0.046

133		IMM039	Immune Hydrops Fetalis	33	0.046

134		GLS004	Glossopharyngeal Neuralgia	33	0.046

135		FNC006	Functional Gastric Disease	32	0.046

136		NRD001	Neurodermatitis	32	0.046

137	P	HRT017	Heart Tumor	32	0.046

138		CLC011	Cloacal Exstrophy	32	0.046

139		CLN006	Colonic Pseudo-Obstruction	31	0.046

140	P	ACT080	Acute Pulmonary Heart Disease	31	0.046

141	c	CHR057	Chronic Laryngitis	31	0.046

142		ALB003	Albinism-Deafness Syndrome	30	0.046

143		NNT005	Neonatal Candidiasis	30	0.046

144	c	ACT072	Acute Laryngitis	30	0.046

145		ACT118	Acute Non Lymphoblastic Leukemia	30	0.046

146		GST004	Gastric Neuroendocrine Neoplasm	30	0.046

147		ISC001	Ischemic Neuropathy	30	0.046

148		BLD041	Bladder Calculus	30	0.046

149		MRG013	Mirage Syndrome	29	0.046

150		PNM003	Pneumatosis Cystoides Intestinalis	29	0.046

151		PHT004	Photoallergic Dermatitis	28	0.046

152		SQM005	Squamous Papillomatosis	28	0.046

153		LRY007	Laryngeal Tuberculosis	28	0.046

154		DNT046	Dental Abscess	28	0.046

155		LWR004	Lower Urinary Tract Calculus	28	0.046

156		RHS001	Rh Isoimmunization	28	0.046

157		GRN011	Granulomatous Gastritis	28	0.046

158		THY001	Thyroid Crisis	27	0.046

159		FNG003	Fungal Esophagitis	27	0.046

160		OCL003	Oculomotor Nerve Paralysis	27	0.046

161		FNC005	Functional Colonic Disease	27	0.046

162		ANS018	Anismus	27	0.046

163		HMD003	Hemidystonia	26	0.046

164		VSL003	Visual Agnosia	26	0.046

165		CHR067	Chronic Intestinal Vascular Insufficiency	26	0.046

166		THR010	Third Cranial Nerve Disease	26	0.046

167		HNM002	Hinman Syndrome	25	0.046

168		GST090	Gastroduodenal Crohn's Disease	25	0.046

169		FBR064	Febrile Infection-Related Epilepsy Syndrome	25	0.046

170		IMM025	Immunoglobulin a Deficiency 2	24	0.046

171	c	GST091	Gastrointestinal Neuroendocrine Benign Tumor	24	0.046

172		INF033	Infancy Electroclinical Syndrome	21	0.046

173		ADT001	Auditory Agnosia	20	0.046

174		TRN017	Transient Neonatal Neutropenia	18	0.046

175	c	ADL079	Adult Heart Tumor	16	0.046

176		AND005	Androgen Insensitivity Syndrome, Mild	16	0.046

177		FTL016	Fetal Edema	15	0.046

178		HRT029	Heart Tumor of the Child	15	0.046

179		TRN013	Transient Neonatal Thrombocytopenia	13	0.046

180	c	KRN003	Kernicterus Due to Isoimmunization	12	0.046