Search results for "leukopenia"

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

224 hits were found for 'leukopenia'

# Family MCID Name MIFTS Score
1
RTC002 Reticular Dysgenesis 50 4.597
2
PRP084 Propionicacidemia 59 3.202
3
P NTR004 Neutropenia 59 2.616
4
WHM001 Whim Syndrome 53 2.264
5
c NTR039 Neutropenia, Severe Congenital 4, Autosomal Recessive 28 2.264
6
FLT011 Felty Syndrome 48 2.264
7
c NTR008 Neutropenia Chronic Familial 14 2.264
8
P THR014 Thrombocytopenia 63 0.343
9
P LKM002 Leukemia 70 0.145
10
c SYS001 Systemic Lupus Erythematosus 87 0.111
11
P HPT021 Hepatitis 74 0.111
12
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.111
13
GRN017 Granulocytopenia 39 0.111
14
P LNG032 Lung Cancer 92 0.103
15
P ART022 Arthritis 73 0.103
16
P LPS004 Lupus Erythematosus 63 0.103
17
LKC003 Leukocyte Disease 45 0.103
18
P RHM011 Rheumatoid Arthritis 87 0.094
19
CRH001 Crohn's Disease 76 0.094
20
P ANR007 Anorexia Nervosa 63 0.094
21
P PNM007 Pneumonia 67 0.094
22
P BRS047 Breast Cancer 100 0.084
23
GNG013 Gingivitis 61 0.084
24
IMM102 Immunodeficiency 14 33 0.084
25
VSC011 Vasculitis 62 0.084
26
ACQ007 Acquired Immunodeficiency Syndrome 60 0.084
27
ADM013 Adamantinoma of Long Bones 57 0.084
28
LYM027 Lymphopenia 54 0.084
29
HMN014 Human Immunodeficiency Virus Infectious Disease 46 0.084
30
BRN106 Burns 52 0.084
31
P APL001 Aplastic Anemia 74 0.073
32
P CMR001 Camurati-Engelmann Disease 63 0.073
33
P PLM037 Pulmonary Hypertension 78 0.073
34
c FNC027 Fanconi Anemia, Complementation Group a 71 0.073
35
DRM006 Dermatitis 58 0.073
36
MTH039 Methylmalonic Aciduria, Mut(0) Type 34 0.073
37
PRP030 Purpura 60 0.073
38
TCK001 Tick-Borne Encephalitis 49 0.073
39
P LYM026 Lymphoblastic Leukemia 60 0.073
40
P PNC044 Pancreatitis 62 0.073
41
c ACT073 Acute Leukemia 61 0.073
42
P ENC004 Encephalitis 60 0.073
43
BCT015 Bacteremia 50 0.073
44
P MYC007 Myocardial Infarction 80 0.059
45
MLR004 Malaria 80 0.059
46
HV1006 Hiv-1 80 0.059
47
WST001 West Syndrome 61 0.059
48
c GCH015 Gaucher Disease, Type I 52 0.059
49
MLN008 Melanoma 61 0.059
50
FMR004 Fumarase Deficiency 38 0.059
51
CHN016 Cohen Syndrome 55 0.059
52
TBR010 Tuberculosis 70 0.059
53
VRL011 Viral Infectious Disease 56 0.059
54
P ADM011 Adams-Oliver Syndrome 51 0.059
55
P HML002 Hemolytic Anemia 60 0.059
56
LVR012 Liver Cirrhosis 71 0.059
57
P GRV001 Graves' Disease 62 0.059
58
SRC014 Sarcoma 66 0.059
59
TYP007 Typhoid Fever 61 0.059
60
MRB001 Marburg Hemorrhagic Fever 41 0.059
61
EBL001 Ebola Hemorrhagic Fever 40 0.059
62
BBS001 Babesiosis 45 0.059
63
CRM001 Crimean-Congo Hemorrhagic Fever 53 0.059
64
LSS003 Lassa Fever 37 0.059
65
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 21 0.059
66
P DRR001 Diarrhea 60 0.059
67
ARG001 Argentine Hemorrhagic Fever 35 0.059
68
MXD005 Mixed Connective Tissue Disease 63 0.059
69
DNG004 Dengue Fever, Protection Against 27 0.059
70
P GRS003 Griscelli Syndrome 48 0.059
71
SPL018 Splenomegaly 45 0.059
72
LKS001 Leukostasis 39 0.059
73
ISC004 Ischemia 56 0.059
74
AGG002 Aggressive Systemic Mastocytosis 42 0.059
75
P CRV039 Cervicitis 45 0.059
76
P PRS040 Prostate Cancer 89 0.042
77
HPT023 Hepatocellular Carcinoma 90 0.042
78
P SCH015 Schizophrenia 78 0.042
79
P PNC035 Pancreatic Cancer 86 0.042
80
P CLR023 Colorectal Cancer 96 0.042
81
P LFR001 Li-Fraumeni Syndrome 79 0.042
82
P OVR042 Ovarian Cancer 73 0.042
83
P RNL014 Renal Cell Carcinoma 80 0.042
84
KPS004 Kaposi Sarcoma 69 0.042
85
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 61 0.042
86
P KDN017 Kidney Cancer 67 0.042
87
P LVR013 Liver Disease 76 0.042
88
ISV001 Isovaleric Acidemia 52 0.042
89
CNG034 Congestive Heart Failure 72 0.042
90
LYS003 Lysinuric Protein Intolerance 51 0.042
91
CHD001 Chediak-Higashi Syndrome 66 0.042
92
c GCH017 Gaucher Disease, Type Iii 44 0.042
93
DYS164 Dyskeratosis Congenita, X-Linked 45 0.042
94
P ALP004 Alport Syndrome 68 0.042
95
DFC004 Deficiency Anemia 64 0.042
96
P MYL005 Myelofibrosis 67 0.042
97
MYL009 Myelodysplastic Syndrome 73 0.042
98
INS024 Insulin-Like Growth Factor I 75 0.042
99
CSY001 C Syndrome 49 0.042
100
ULC004 Ulcerative Colitis 74 0.042
101
FLT009 Folate Malabsorption, Hereditary 31 0.042
102
SVR031 Severe Combined Immunodeficiency, Athabascan Type 37 0.042
103
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 31 0.042
104
CHL071 Child Syndrome 58 0.042
105
SVR006 Severe Combined Immunodeficiency Due to Ada Deficiency 35 0.042
106
NTR005 Nutritional Deficiency Disease 51 0.042
107
SVR033 Severe Combined Immunodeficiency, B Cell-Negative 36 0.042
108
ADL002 Adult Syndrome 53 0.042
109
P ASP006 Aspergillosis 61 0.042
110
SVR029 Severe Combined Immunodeficiency, T Cell-Negative, B-Cell/natural Killer-Cell Positive 37 0.042
111
c HPT001 Hepatitis C 68 0.042
112
SVR004 Severe Combined Immunodeficiency 71 0.042
113
P FNC043 Fanconi Anemia, Complementation Group E 45 0.042
114
HRP004 Herpes Zoster 56 0.042
115
c ATM010 Autoimmune Hemolytic Anemia 59 0.042
116
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 34 0.042
117
SVR032 Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation 26 0.042
118
PNM001 Pneumocystosis 50 0.042
119
P SJG001 Sjogren's Syndrome 55 0.042
120
P LYM118 Lymphoma 68 0.042
121
c HPT016 Hepatitis B 61 0.042
122
c DYS143 Dyskeratosis Congenita, Autosomal Dominant 2 32 0.042
123
P MYL006 Myeloid Leukemia 67 0.042
124
P FNC044 Fanconi Anemia, Complementation Group C 43 0.042
125
c THR037 Thrombocytopenia 2 36 0.042
126
BNM001 Bone Marrow Cancer 56 0.042
127
GHS004 Ghosal Hematodiaphyseal Syndrome 25 0.042
128
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 28 0.042
129
P INF038 Influenza 71 0.042
130
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 27 0.042
131
P THL005 Thalassemia 61 0.042
132
c FNC042 Fanconi Anemia, Complementation Group D2 32 0.042
133
c FNC024 Fanconi Anemia, Complementation Group D1 24 0.042
134
KDS001 Kid Syndrome 53 0.042
135
SPL012 Splenic Disease 48 0.042
136
SPN041 Spinal Cord Disease 50 0.042
137
INC022 Inclusion-Cell Disease 46 0.042
138
c FNC032 Fanconi Anemia, Complementation Group B 41 0.042
139
c DYS147 Dyskeratosis Congenita, Autosomal Dominant 3 24 0.042
140
c FNC048 Fanconi Anemia, Complementation Group O 23 0.042
141
P HYP076 Hyperthyroidism 59 0.042
142
ATH003 Atherosclerosis 63 0.042
143
c FNC028 Fanconi Anemia, Complementation Group L 27 0.042
144
c FNC047 Fanconi Anemia, Complementation Group Q 24 0.042
145
c FNC023 Fanconi Anemia, Complementation Group N 27 0.042
146
c FNC046 Fanconi Anemia, Complementation Group P 24 0.042
147
P MNN013 Meningitis 66 0.042
148
c FNC025 Fanconi Anemia, Complementation Group J 27 0.042
149
PSD007 Pseudomyxoma Peritonei 51 0.042
150
FNC030 Fanconi Anemia, Complementation Group G 24 0.042
151
P OST001 Osteopetrosis 63 0.042
152
P TXP001 Toxoplasmosis 61 0.042
153
TLR001 Tularemia 46 0.042
154
c FNC045 Fanconi Anemia, Complementation Group F 38 0.042
155
c FNC029 Fanconi Anemia, Complementation Group I 26 0.042
156
c SYS004 Systemic Mastocytosis 60 0.042
157
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 41 0.042
158
HMT002 Hematologic Cancer 62 0.042
159
CRY005 Cryptococcosis 50 0.042
160
P PRT013 Portal Hypertension 61 0.042
161
EHR002 Ehrlichiosis 44 0.042
162
STN012 Sting-Associated Vasculopathy, Infantile-Onset 21 0.042
163
NTR006 Neutrophil Immunodeficiency Syndrome 36 0.042
164
SVR066 Severe Combined Immunodeficiency, X-Linked 43 0.042
165
c DMN018 Diamond-Blackfan Anemia 5 29 0.042
166
OST003 Osteonecrosis 45 0.042
167
RTN017 Retinal Detachment 58 0.042
168
CLR007 Colorado Tick Fever 33 0.042
169
GST045 Gastroenteritis 59 0.042
170
SPL011 Spleen Cancer 38 0.042
171
TRP004 Tropical Sprue 36 0.042
172
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.042
173
BNM011 Bone Marrow Failure Syndrome 2 29 0.042
174
DWR001 Dwarfism 42 0.042
175
HMG002 Hemoglobinuria 49 0.042
176
c CHR092 Chronic Myeloproliferative Disease 50 0.042
177
P FNC052 Fanconi Anemia, Complementation Group T 19 0.042
178
BLM002 Bulimia Nervosa 54 0.042
179
PLY112 Polyarteritis Nodosa, Childhood-Onset 22 0.042
180
BRS051 Breast Disease 57 0.042
181
MYL004 Myelodysplastic Myeloproliferative Cancer 46 0.042
182
SCD002 Scid, Autosomal Recessive, T-Negative/b-Positive Type 21 0.042
183
KKC001 Kikuchi Disease 34 0.042
184
PLR001 Pleural Tuberculosis 47 0.042
185
CNG028 Congenital Hypoplastic Anemia 48 0.042
186
MST005 Mastitis 53 0.042
187
c CNG027 Congenital Hemolytic Anemia 46 0.042
188
HMG005 Hemoglobinopathy 49 0.042
189
P END047 Endophthalmitis 46 0.042
190
PRX008 Paroxysmal Cold Hemoglobinuria 26 0.042
191
P ALC004 Alcohol Abuse 57 0.042
192
GDS001 Good Syndrome 46 0.042
193
PLV003 Pelvic Inflammatory Disease 52 0.042
194
DRG003 Drug Dependence 53 0.042
195
P NRP001 Neuropathy 57 0.042
196
LPM005 Lipomatosis 46 0.042
197
CHR463 Chronic Actinic Dermatitis 33 0.042
198
CLT003 Colitis 56 0.042
199
BLD053 Blood Platelet Disease 44 0.042
200
PRS047 Prostatitis 56 0.042
201
ASP003 Aseptic Meningitis 51 0.042
202
c VRL005 Viral Pneumonia 44 0.042
203
c ACT075 Acute Myocardial Infarction 61 0.042
204
c VRL017 Viral Hemorrhagic Fever 28 0.042
205
TXC007 Toxic Pneumonitis 36 0.042
206
HMN032 Human Herpesvirus 8 42 0.042
207
HYP266 Hypoxia 55 0.042
208
CHR078 Chorioretinitis 41 0.042
209
ANC002 Anca-Associated Vasculitis 43 0.042
210
EXF003 Exfoliative Dermatitis 25 0.042
211
INS009 Insulin-Resistance Type B 21 0.042
212
SHW001 Shwartzman Phenomenon 38 0.042
213
TYP004 Typhoidal Tularemia 11 0.042
214
ARG004 Argyria 20 0.042
215
THL017 Thalassemia Intermedia 38 0.042
216
RTN023 Retinitis 49 0.042
217
c PRM225 Primary Thrombocytopenia 42 0.042
218
OST115 Osteonecrosis of the Jaw 37 0.042
219
THL010 Thalassemia Minor 38 0.042
220
BNS002 Bone Structure Disease 37 0.042
221
c PRM023 Pre-Malignant Neoplasm 42 0.042
222
MNN021 Meningococcemia 35 0.042
223
THL018 Thalassemia Major 31 0.042
224
CD4004 Cd4 Deficiency 15 0.042