Search results for alloimmunization

208 hits were found for alloimmunization

#	Family	MCID	Name	MIFTS	Score
1		FTL012	Fetal and Neonatal Alloimmune Thrombocytopenia	36	4.968

2	c	CNG407	Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization	10	4.581

3	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	53	3.995

4		NNT054	Neonatal Alloimmune Neutropenia	15	3.466

5		HML043	Hemolytic Disease of the Newborn with Kell Alloimmunization	4	3.262

6		HMC038	Hemochromatosis, Neonatal	38	2.458

7		THR100	Thrombocytopenic Purpura, Autoimmune	57	2.334

8	P	THR014	Thrombocytopenia	65	0.399

9	P	NTR004	Neutropenia	60	0.225

10		SCK005	Sickle Cell Disease	54	0.162

11	P	THL005	Thalassemia	65	0.143

12		PRP030	Purpura	61	0.114

13		SCK003	Sickle Cell Anemia	73	0.106

14		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	63	0.106

15	P	HML002	Hemolytic Anemia	62	0.106

16	P	LVR013	Liver Disease	76	0.097

17		HYD012	Hydrops Fetalis	50	0.097

18		THR035	Thrombasthenia	46	0.097

19		HYD059	Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect	34	0.097

20	P	GRF003	Graft-Versus-Host Disease	72	0.087

21		GLN010	Glanzmann Thrombasthenia	66	0.087

22	P	MMB011	Membranous Nephropathy	55	0.087

23		PNC001	Pancytopenia	50	0.087

24		HMS001	Hemosiderosis	50	0.087

25		BLD053	Blood Platelet Disease	45	0.087

26	P	LKM002	Leukemia	75	0.075

27		AGN016	Aging	65	0.075

28		HMT018	Hematopoietic Stem Cell Transplantation	58	0.075

29		IMM158	Immune Suppression	57	0.075

30	c	ANM038	Anemia, Autoimmune Hemolytic	56	0.075

31		END072	Endotheliitis	46	0.075

32	P	HPT021	Hepatitis	75	0.061

33		APL001	Aplastic Anemia	74	0.061

34	c	BTT014	Beta-Thalassemia	70	0.061

35	P	MYL006	Myeloid Leukemia	69	0.061

36	c	HMP029	Hemophilia a	69	0.061

37	P	ANR048	Aniridia 1	68	0.061

38	c	CHR417	Chronic Graft Versus Host Disease	65	0.061

39	P	CHR285	Chronic Myelomonocytic Leukemia	63	0.061

40	P	HMP007	Hemophilia	61	0.061

41	P	GLM007	Glomerulonephritis	61	0.061

42	c	ALP101	Alpha-Thalassemia	60	0.061

43	P	BRN019	Bernard-Soulier Syndrome	60	0.061

44	P	PRN026	Porencephaly	50	0.061

45		PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	48	0.061

46	P	SDR002	Siderosis	48	0.061

47	P	BLD051	Blood Coagulation Disease	38	0.061

48	P	BLD124	Bleeding Disorder, Platelet-Type, 11	38	0.061

49	c	BLD140	Blood Group, I System	37	0.061

50	c	PRM225	Primary Thrombocytopenia	37	0.061

51	c	MLT151	Multiple Mitochondrial Dysfunctions Syndrome 5	36	0.061

52		FTL004	Fetal Erythroblastosis	35	0.061

53		ATM012	Autoimmune Disease of Blood	31	0.061

54		ALR002	Al-Raqad Syndrome	30	0.061

55		PDG002	Pdgfrb-Associated Chronic Eosinophilic Leukemia	29	0.061

56		ATS208	Autosomal Dominant Macrothrombocytopenia	27	0.061

57		ANR038	Anorexia Nervosa 1	21	0.061

58	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	21	0.061

59		BLD137	Blood Group--Ahonen	17	0.061

60	P	LNG032	Lung Cancer	99	0.043

61	c	SYS001	Systemic Lupus Erythematosus	86	0.043

62	P	MLT020	Multiple Sclerosis	85	0.043

63	c	LKM061	Leukemia, Acute Myeloid	81	0.043

64	P	ART022	Arthritis	77	0.043

65		MYL009	Myelodysplastic Syndrome	75	0.043

66		ALP046	Alport Syndrome, X-Linked	74	0.043

67		PFF001	Pfeiffer Syndrome	74	0.043

68		LVR012	Liver Cirrhosis	73	0.043

69	P	HRD008	Hereditary Hemorrhagic Telangiectasia	72	0.043

70		VSC007	Vascular Disease	71	0.043

71	c	HMC039	Hemochromatosis, Type 1	71	0.043

72	P	LYM118	Lymphoma	71	0.043

73		BRC012	Brucellosis	71	0.043

74	P	ESS003	Essential Thrombocythemia	71	0.043

75	P	PNM007	Pneumonia	70	0.043

76		PRT037	Pertussis	70	0.043

77	P	LPS004	Lupus Erythematosus	69	0.043

78	P	KDN018	Kidney Disease	69	0.043

79	P	CHR012	Chronic Granulomatous Disease	69	0.043

80		LNG099	Lung Disease	67	0.043

81	P	CNJ013	Conjunctivitis	67	0.043

82	P	PRD008	Periodontitis	67	0.043

83		ATM095	Autoimmune Disease	66	0.043

84	P	ENC004	Encephalitis	66	0.043

85	c	DNG003	Dengue Disease	66	0.043

86	c	PRC016	Pre-Eclampsia	65	0.043

87		TTN003	Tetanus	65	0.043

88		VLC001	Velocardiofacial Syndrome	64	0.043

89		HYP066	Hyperglycemia	64	0.043

90		CRB011	Cerebrotendinous Xanthomatosis	64	0.043

91		ACT119	Acute Promyelocytic Leukemia	64	0.043

92	c	HPT003	Hepatitis a	63	0.043

93		DPH001	Diphtheria	63	0.043

94	c	ATM011	Autoimmune Hepatitis	63	0.043

95	c	ADL017	Adult T-Cell Leukemia	63	0.043

96	P	MYS005	Myositis	63	0.043

97	P	THR005	Thrombotic Thrombocytopenic Purpura	63	0.043

98		INT066	Interstitial Lung Disease	63	0.043

99	P	ART021	Arteriosclerosis	62	0.043

100		GST033	Gestational Diabetes	62	0.043

101	P	GRV001	Graves' Disease	62	0.043

102	P	ACT074	Acute Lymphocytic Leukemia	61	0.043

103		MCS002	Mucositis	61	0.043

104		VNW001	Von Willebrand's Disease	61	0.043

105		TNS005	Tonsillitis	61	0.043

106		CHL068	Cholestasis	60	0.043

107	P	PLY018	Polycythemia	60	0.043

108		BRN012	Bronchiolitis Obliterans	60	0.043

109		BRN002	Bronchiolitis	59	0.043

110	P	ANT006	Antiphospholipid Syndrome	59	0.043

111		LGG001	Legg-Calve-Perthes Disease	59	0.043

112		JPN002	Japanese Encephalitis	59	0.043

113		RLP002	Relapsing-Remitting Multiple Sclerosis	59	0.043

114		THR009	Thrombocytopenia-Absent Radius Syndrome	58	0.043

115		LYM040	Lymphoblastic Lymphoma	58	0.043

116	P	THR015	Thrombophilia	58	0.043

117		URN009	Urinary System Disease	58	0.043

118	P	ECL001	Eclampsia	57	0.043

119	P	LPD010	Lipodystrophy	57	0.043

120		VND007	Van Der Woude Syndrome 1	57	0.043

121		SPT005	Spotted Fever	57	0.043

122		INF034	Infective Endocarditis	56	0.043

123		HST011	Histoplasmosis	56	0.043

124	P	THY032	Thyroiditis	56	0.043

125		GRY002	Gray Platelet Syndrome	56	0.043

126		THR004	Thrombocytosis	55	0.043

127	P	SYP003	Syphilis	55	0.043

128		INT007	Intermediate Coronary Syndrome	55	0.043

129	P	TRC086	Trichohepatoenteric Syndrome 1	54	0.043

130		MCR004	Macroglobulinemia	54	0.043

131	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	54	0.043

132		ALL009	Allergic Conjunctivitis	53	0.043

133		XNT003	Xanthomatosis	53	0.043

134		RNP003	Renpenning Syndrome 1	53	0.043

135		HMG005	Hemoglobinopathy	53	0.043

136		HPT082	Hepatic Adenomas, Familial	52	0.043

137		CHR005	Chorioamnionitis	52	0.043

138		PRR002	Pure Red-Cell Aplasia	52	0.043

139	c	GRV008	Graves Disease 1	52	0.043

140	c	AMG001	Amegakaryocytic Thrombocytopenia, Congenital	51	0.043

141		BBS001	Babesiosis	51	0.043

142	c	ACQ014	Acquired Hemophilia	51	0.043

143		CLD007	Cold Agglutinin Disease	50	0.043

144	P	MRC003	Mercury Poisoning	50	0.043

145	P	TCL004	T-Cell Leukemia	50	0.043

146		THR013	Thoracic Outlet Syndrome	50	0.043

147	c	ART119	Arthrogryposis, Distal, Type 5	49	0.043

148		MTC056	Mitochondrial Dna Depletion Syndrome 4a	49	0.043

149		AND020	Androgen Insensitivity, Partial	49	0.043

150		GRN017	Granulocytopenia	49	0.043

151		HPR003	Heparin-Induced Thrombocytopenia	48	0.043

152	P	PLM085	Pulmonary Hemosiderosis	48	0.043

153		HNC001	Henoch-Schoenlein Purpura	48	0.043

154		BSC001	Buschke-Ollendorff Syndrome	48	0.043

155		ISC002	Ischemic Optic Neuropathy	48	0.043

156		PLC008	Placenta Disease	48	0.043

157		CRN017	Coronary Thrombosis	48	0.043

158		LKC005	Leukocyte Adhesion Deficiency, Type Iii	47	0.043

159		PTT041	Pituitary Stalk Interruption Syndrome	47	0.043

160		PTT004	Pituitary Apoplexy	47	0.043

161		EHR002	Ehrlichiosis	45	0.043

162	P	ACQ022	Acquired Generalized Lipodystrophy	45	0.043

163	c	ACQ042	Acquired Hemophilia a	44	0.043

164		RTR011	Retroperitoneal Fibrosis	43	0.043

165		RCK002	Rocky Mountain Spotted Fever	42	0.043

166		SPL012	Splenic Disease	42	0.043

167		EXN001	Exanthema Subitum	42	0.043

168	c	HMC010	Hemochromatosis, Type 3	42	0.043

169		GLC106	Glucocorticoid Resistance, Generalized	41	0.043

170	c	ALZ056	Alzheimer Disease 3	41	0.043

171		ADP007	Adie Pupil	41	0.043

172	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	41	0.043

173		MYH012	Myhre Syndrome	41	0.043

174	P	PRC031	Preeclampsia/eclampsia 1	41	0.043

175	c	CNG033	Congenital Syphilis	40	0.043

176		LYM010	Lymph Node Tuberculosis	40	0.043

177		PMP002	Pemphigoid Gestationis	40	0.043

178		CPL005	Capillary Disease	38	0.043

179		HST017	Histiocytosis-Lymphadenopathy Plus Syndrome	38	0.043

180		CRT004	Carotid Artery Thrombosis	37	0.043

181		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	37	0.043

182	c	THR090	Thrombocythemia 1	37	0.043

183	P	ANX007	Anauxetic Dysplasia 1	36	0.043

184		ANG037	Angiomatosis	36	0.043

185		PRC005	Pericardial Tuberculosis	35	0.043

186		ASY002	Asymptomatic Neurosyphilis	34	0.043

187	c	BLD152	Bleeding Disorder, Platelet-Type, 16	34	0.043

188	c	DYS174	Dyskeratosis Congenita, Autosomal Dominant 6	34	0.043

189		MNG003	Mungan Syndrome	34	0.043

190		SCL025	Scleromyxedema	34	0.043

191		ACT118	Acute Non Lymphoblastic Leukemia	32	0.043

192	c	PRM022	Primary Syphilis	32	0.043

193	c	THR111	Thrombocytopenia 3	32	0.043

194		ART110	Arteritic Anterior Ischemic Optic Neuropathy	31	0.043

195		OCL033	Oculocerebral Syndrome with Hypopigmentation	31	0.043

196	c	SRC023	Sarcoidosis 2	30	0.043

197	c	INH004	Inherited Blood Coagulation Disease	29	0.043

198		TRT002	Tertiary Neurosyphilis	29	0.043

199		LTN001	Latent Syphilis	29	0.043

200		TRT003	Tertiary Syphilis	29	0.043

201		BLD052	Blood Group Incompatibility	26	0.043

202	c	ERL002	Early Congenital Syphilis	24	0.043

203		BLD163	Blood Group, Dombrock System	23	0.043

204		MXD035	Mixed-Type Autoimmune Hemolytic Anemia	22	0.043

205		TRN017	Transient Neonatal Neutropenia	19	0.043

206		IMM162	Immunoglobulin E Concentration, Serum	16	0.043

207		LRY021	Laryngeal Adductor Paralysis	15	0.043

208		TRN013	Transient Neonatal Thrombocytopenia	11	0.043