Search results for "leukopenia"

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

221 hits were found for 'leukopenia'

# Family MCID Name MIFTS Score
1
RTC002 Reticular Dysgenesis 49 4.597
2
PRP084 Propionicacidemia 58 3.201
3
P NTR004 Neutropenia 59 2.617
4
WHM001 Whim Syndrome 52 2.264
5
FLT011 Felty Syndrome 45 2.264
6
c NTR039 Neutropenia, Severe Congenital 4, Autosomal Recessive 28 2.264
7
c NTR008 Neutropenia Chronic Familial 16 2.264
8
P THR014 Thrombocytopenia 64 0.345
9
P LKM002 Leukemia 70 0.146
10
c SYS001 Systemic Lupus Erythematosus 87 0.111
11
CRH001 Crohn's Disease 76 0.111
12
P HPT021 Hepatitis 70 0.111
13
GRN017 Granulocytopenia 42 0.111
14
P LNG032 Lung Cancer 94 0.103
15
P ART022 Arthritis 75 0.103
16
P LPS004 Lupus Erythematosus 63 0.103
17
LKC003 Leukocyte Disease 47 0.103
18
P RHM011 Rheumatoid Arthritis 88 0.094
19
P PNM007 Pneumonia 66 0.094
20
P ANR007 Anorexia Nervosa 63 0.094
21
P BRS047 Breast Cancer 100 0.084
22
HV1006 Hiv-1 82 0.084
23
VSC011 Vasculitis 62 0.084
24
PRM097 Primary Immunodeficiency Disease 61 0.084
25
GNG013 Gingivitis 60 0.084
26
ADM013 Adamantinoma of Long Bones 59 0.084
27
LYM027 Lymphopenia 54 0.084
28
BRN106 Burns 52 0.084
29
HMN014 Human Immunodeficiency Virus Infectious Disease 49 0.084
30
P PLM037 Pulmonary Hypertension 79 0.073
31
P APL001 Aplastic Anemia 73 0.073
32
c FNC027 Fanconi Anemia, Complementation Group a 73 0.073
33
HMT002 Hematologic Cancer 64 0.073
34
c ACT073 Acute Leukemia 62 0.073
35
DRM006 Dermatitis 61 0.073
36
P ENC004 Encephalitis 61 0.073
37
P PNC044 Pancreatitis 60 0.073
38
P LYM026 Lymphoblastic Leukemia 60 0.073
39
P CMR001 Camurati-Engelmann Disease 59 0.073
40
PRP030 Purpura 59 0.073
41
TCK001 Tick-Borne Encephalitis 49 0.073
42
BCT015 Bacteremia 48 0.073
43
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.073
44
MTH039 Methylmalonic Aciduria, Mut(0) Type 34 0.073
45
MLR004 Malaria 79 0.060
46
P MYC007 Myocardial Infarction 79 0.060
47
TBR010 Tuberculosis 69 0.060
48
LVR012 Liver Cirrhosis 67 0.060
49
SRC014 Sarcoma 66 0.060
50
c GCH015 Gaucher Disease, Type I 66 0.060
51
WST001 West Syndrome 61 0.060
52
P GRV001 Graves' Disease 61 0.060
53
TYP007 Typhoid Fever 61 0.060
54
P HML002 Hemolytic Anemia 60 0.060
55
VRL011 Viral Infectious Disease 59 0.060
56
MSS002 Mass Syndrome 59 0.060
57
ISC004 Ischemia 59 0.060
58
P GRS014 Griscelli Syndrome, Type 2 55 0.060
59
CHN016 Cohen Syndrome 55 0.060
60
CRM001 Crimean-Congo Hemorrhagic Fever 54 0.060
61
P DRR001 Diarrhea 51 0.060
62
P ADM011 Adams-Oliver Syndrome 48 0.060
63
BBS001 Babesiosis 45 0.060
64
P CRV039 Cervicitis 44 0.060
65
SPL018 Splenomegaly 44 0.060
66
AGG002 Aggressive Systemic Mastocytosis 42 0.060
67
MRB001 Marburg Hemorrhagic Fever 41 0.060
68
EBL001 Ebola Hemorrhagic Fever 41 0.060
69
LKS001 Leukostasis 39 0.060
70
FMR004 Fumarase Deficiency 38 0.060
71
LSS003 Lassa Fever 38 0.060
72
ARG001 Argentine Hemorrhagic Fever 34 0.060
73
DNG004 Dengue Fever, Protection Against 28 0.060
74
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 23 0.060
75
P CLR023 Colorectal Cancer 97 0.042
76
HPT023 Hepatocellular Carcinoma 91 0.042
77
P PRS040 Prostate Cancer 89 0.042
78
P PNC035 Pancreatic Cancer 85 0.042
79
P RNL014 Renal Cell Carcinoma 81 0.042
80
P SCH015 Schizophrenia 76 0.042
81
P OVR042 Ovarian Cancer 75 0.042
82
ULC004 Ulcerative Colitis 75 0.042
83
INS024 Insulin-Like Growth Factor I 74 0.042
84
MYL009 Myelodysplastic Syndrome 74 0.042
85
P INF038 Influenza 74 0.042
86
CMP005 Campomelic Dysplasia 72 0.042
87
P LVR013 Liver Disease 72 0.042
88
CNG034 Congestive Heart Failure 71 0.042
89
P LYM118 Lymphoma 70 0.042
90
P ALP004 Alport Syndrome 68 0.042
91
c HPT001 Hepatitis C 68 0.042
92
SVR004 Severe Combined Immunodeficiency 68 0.042
93
P MYL005 Myelofibrosis 67 0.042
94
P KDN017 Kidney Cancer 67 0.042
95
P MYL006 Myeloid Leukemia 67 0.042
96
KPS004 Kaposi Sarcoma 66 0.042
97
P MNN013 Meningitis 65 0.042
98
DFC004 Deficiency Anemia 65 0.042
99
c HPT016 Hepatitis B 64 0.042
100
CHD001 Chediak-Higashi Syndrome 64 0.042
101
ATH003 Atherosclerosis 62 0.042
102
P OST001 Osteopetrosis 62 0.042
103
P THL005 Thalassemia 61 0.042
104
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 61 0.042
105
c ACT075 Acute Myocardial Infarction 60 0.042
106
P ASP006 Aspergillosis 60 0.042
107
P TXP001 Toxoplasmosis 60 0.042
108
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.042
109
c ATM010 Autoimmune Hemolytic Anemia 60 0.042
110
P NRP001 Neuropathy 60 0.042
111
GST045 Gastroenteritis 60 0.042
112
P ALC004 Alcohol Abuse 60 0.042
113
P PRT013 Portal Hypertension 59 0.042
114
CLT003 Colitis 59 0.042
115
c SYS004 Systemic Mastocytosis 59 0.042
116
CHL071 Child Syndrome 58 0.042
117
RTN017 Retinal Detachment 57 0.042
118
SVR066 Severe Combined Immunodeficiency, X-Linked 57 0.042
119
HRP004 Herpes Zoster 56 0.042
120
P HYP076 Hyperthyroidism 56 0.042
121
PRS047 Prostatitis 56 0.042
122
ALP008 Alopecia 55 0.042
123
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.042
124
HYP266 Hypoxia 55 0.042
125
BLM002 Bulimia Nervosa 54 0.042
126
PLV003 Pelvic Inflammatory Disease 53 0.042
127
DRG003 Drug Dependence 53 0.042
128
P SJG001 Sjogren's Syndrome 53 0.042
129
KDS001 Kid Syndrome 53 0.042
130
BNM001 Bone Marrow Cancer 52 0.042
131
P PNC001 Pancytopenia 52 0.042
132
MST005 Mastitis 52 0.042
133
ISV001 Isovaleric Acidemia 51 0.042
134
ASP003 Aseptic Meningitis 51 0.042
135
CRY005 Cryptococcosis 50 0.042
136
HMG005 Hemoglobinopathy 50 0.042
137
PNM001 Pneumocystosis 50 0.042
138
LYS003 Lysinuric Protein Intolerance 50 0.042
139
CSY001 C Syndrome 49 0.042
140
HMG002 Hemoglobinuria 49 0.042
141
CNG028 Congenital Hypoplastic Anemia 49 0.042
142
RTN023 Retinitis 49 0.042
143
c CNG027 Congenital Hemolytic Anemia 48 0.042
144
SPL012 Splenic Disease 47 0.042
145
PSD007 Pseudomyxoma Peritonei 47 0.042
146
PLR001 Pleural Tuberculosis 47 0.042
147
LPM005 Lipomatosis 47 0.042
148
MYL004 Myelodysplastic Myeloproliferative Cancer 47 0.042
149
DWR001 Dwarfism 46 0.042
150
BLD053 Blood Platelet Disease 46 0.042
151
P END047 Endophthalmitis 46 0.042
152
HMN032 Human Herpesvirus 8 46 0.042
153
OST003 Osteonecrosis 45 0.042
154
GDS001 Good Syndrome 45 0.042
155
c GCH017 Gaucher Disease, Type Iii 45 0.042
156
P FNC043 Fanconi Anemia, Complementation Group E 45 0.042
157
P FNC044 Fanconi Anemia, Complementation Group C 44 0.042
158
DYS164 Dyskeratosis Congenita, X-Linked 44 0.042
159
c PRM023 Pre-Malignant Neoplasm 43 0.042
160
THL018 Thalassemia Major 42 0.042
161
c PRM225 Primary Thrombocytopenia 42 0.042
162
c VRL005 Viral Pneumonia 42 0.042
163
TLR001 Tularemia 42 0.042
164
CHR078 Chorioretinitis 41 0.042
165
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 41 0.042
166
c FNC032 Fanconi Anemia, Complementation Group B 41 0.042
167
EHR002 Ehrlichiosis 41 0.042
168
ANC002 Anca-Associated Vasculitis 41 0.042
169
THL017 Thalassemia Intermedia 40 0.042
170
NTR005 Nutritional Deficiency Disease 39 0.042
171
MNN021 Meningococcemia 38 0.042
172
THL010 Thalassemia Minor 38 0.042
173
SHW001 Shwartzman Phenomenon 37 0.042
174
SPL011 Spleen Cancer 37 0.042
175
OST115 Osteonecrosis of the Jaw 37 0.042
176
c THR037 Thrombocytopenia 2 37 0.042
177
TRP004 Tropical Sprue 36 0.042
178
c FNC045 Fanconi Anemia, Complementation Group F 36 0.042
179
SVR006 Severe Combined Immunodeficiency Due to Ada Deficiency 36 0.042
180
NTR006 Neutrophil Immunodeficiency Syndrome 36 0.042
181
SVR031 Severe Combined Immunodeficiency, Athabascan Type 36 0.042
182
TXC007 Toxic Pneumonitis 36 0.042
183
CLR007 Colorado Tick Fever 35 0.042
184
SVR033 Severe Combined Immunodeficiency, B Cell-Negative 35 0.042
185
c FNC042 Fanconi Anemia, Complementation Group D2 35 0.042
186
SVR029 Severe Combined Immunodeficiency, T Cell-Negative, B-Cell/natural Killer-Cell Positive 35 0.042
187
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 34 0.042
188
CHR463 Chronic Actinic Dermatitis 33 0.042
189
KKC001 Kikuchi Disease 33 0.042
190
c VRL017 Viral Hemorrhagic Fever 32 0.042
191
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 31 0.042
192
c DMN018 Diamond-Blackfan Anemia 5 29 0.042
193
FLT009 Folate Malabsorption, Hereditary 29 0.042
194
c FNC028 Fanconi Anemia, Complementation Group L 29 0.042
195
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 29 0.042
196
c FNC024 Fanconi Anemia, Complementation Group D1 28 0.042
197
c DYS143 Dyskeratosis Congenita, Autosomal Dominant 2 27 0.042
198
c FNC029 Fanconi Anemia, Complementation Group I 27 0.042
199
c FNC023 Fanconi Anemia, Complementation Group N 27 0.042
200
EXF003 Exfoliative Dermatitis 27 0.042
201
MRG013 Mirage Syndrome 26 0.042
202
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 26 0.042
203
BNM011 Bone Marrow Failure Syndrome 2 26 0.042
204
c FNC046 Fanconi Anemia, Complementation Group P 25 0.042
205
PRX008 Paroxysmal Cold Hemoglobinuria 25 0.042
206
SVR032 Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation 25 0.042
207
c FNC025 Fanconi Anemia, Complementation Group J 25 0.042
208
GHS004 Ghosal Hematodiaphyseal Syndrome 25 0.042
209
c DYS147 Dyskeratosis Congenita, Autosomal Dominant 3 24 0.042
210
FNC030 Fanconi Anemia, Complementation Group G 24 0.042
211
c FNC047 Fanconi Anemia, Complementation Group Q 23 0.042
212
INS009 Insulin-Resistance Type B 22 0.042
213
c FNC048 Fanconi Anemia, Complementation Group O 22 0.042
214
c THR110 Thrombocytopenia 6 22 0.042
215
PLY112 Polyarteritis Nodosa, Childhood-Onset 22 0.042
216
STN012 Sting-Associated Vasculopathy, Infantile-Onset 22 0.042
217
ARG004 Argyria 19 0.042
218
P FNC052 Fanconi Anemia, Complementation Group T 19 0.042
219
SCD002 Scid, Autosomal Recessive, T-Negative/b-Positive Type 17 0.042
220
CD4004 Cd4 Deficiency 17 0.042
221
TYP004 Typhoidal Tularemia 11 0.042