Search results for leukopenia

235 hits were found for leukopenia

# Family MCID Name MIFTS Score
1
RTC002 Reticular Dysgenesis 50 5.132
2
PRP084 Propionicacidemia 58 3.205
3
P NTR004 Neutropenia 59 2.629
4
WHM001 Whim Syndrome 53 2.267
5
FLT011 Felty Syndrome 46 2.267
6
c NTR039 Neutropenia, Severe Congenital 4, Autosomal Recessive 27 2.267
7
c NTR008 Neutropenia Chronic Familial 14 2.267
8
P THR014 Thrombocytopenia 64 0.339
9
P LKM002 Leukemia 71 0.149
10
P LNG032 Lung Cancer 95 0.109
11
c SYS001 Systemic Lupus Erythematosus 86 0.109
12
CRH001 Crohn's Disease 75 0.109
13
P HPT021 Hepatitis 69 0.109
14
GRN017 Granulocytopenia 44 0.109
15
P ART022 Arthritis 75 0.101
16
P LPS004 Lupus Erythematosus 64 0.101
17
LKC003 Leukocyte Disease 43 0.101
18
P RHM011 Rheumatoid Arthritis 89 0.092
19
P PNM007 Pneumonia 68 0.092
20
P INF037 Inflammatory Bowel Disease 63 0.092
21
P ANR007 Anorexia Nervosa 61 0.092
22
P BRS047 Breast Cancer 100 0.083
23
VSC011 Vasculitis 62 0.083
24
GNG013 Gingivitis 61 0.083
25
ACQ007 Acquired Immunodeficiency Syndrome 60 0.083
26
PRM097 Primary Immunodeficiency Disease 60 0.083
27
ADM013 Adamantinoma of Long Bones 57 0.083
28
LYM027 Lymphopenia 56 0.083
29
BRN106 Burns 52 0.083
30
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.083
31
P PLM037 Pulmonary Hypertension 79 0.072
32
P APL001 Aplastic Anemia 75 0.072
33
c FNC027 Fanconi Anemia, Complementation Group a 71 0.072
34
TBR010 Tuberculosis 70 0.072
35
DRM006 Dermatitis 66 0.072
36
HMT002 Hematologic Cancer 64 0.072
37
P ENC004 Encephalitis 63 0.072
38
P LYM026 Lymphoblastic Leukemia 62 0.072
39
P PNC044 Pancreatitis 61 0.072
40
c ACT073 Acute Leukemia 60 0.072
41
PRP030 Purpura 58 0.072
42
P CMR001 Camurati-Engelmann Disease 58 0.072
43
MCS002 Mucositis 55 0.072
44
TCK001 Tick-Borne Encephalitis 50 0.072
45
BCT015 Bacteremia 48 0.072
46
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.072
47
MTH039 Methylmalonic Aciduria, Mut(0) Type 34 0.072
48
MLR004 Malaria 83 0.058
49
HV1006 Hiv-1 80 0.058
50
P MYC007 Myocardial Infarction 79 0.058
51
P ALP004 Alport Syndrome 69 0.058
52
LVR012 Liver Cirrhosis 67 0.058
53
SRC014 Sarcoma 66 0.058
54
MLN008 Melanoma 62 0.058
55
P HML002 Hemolytic Anemia 62 0.058
56
MXD005 Mixed Connective Tissue Disease 62 0.058
57
ISC004 Ischemia 61 0.058
58
c SRC025 Sarcoidosis 1 61 0.058
59
TYP007 Typhoid Fever 61 0.058
60
P DRR001 Diarrhea 60 0.058
61
P GRV001 Graves' Disease 59 0.058
62
c GCH015 Gaucher Disease, Type I 59 0.058
63
WST001 West Syndrome 57 0.058
64
VRL011 Viral Infectious Disease 55 0.058
65
CRM001 Crimean-Congo Hemorrhagic Fever 55 0.058
66
CHN016 Cohen Syndrome 54 0.058
67
P GRS003 Griscelli Syndrome 51 0.058
68
P ADM011 Adams-Oliver Syndrome 48 0.058
69
BBS001 Babesiosis 46 0.058
70
P CRV039 Cervicitis 45 0.058
71
SPL018 Splenomegaly 44 0.058
72
AGG002 Aggressive Systemic Mastocytosis 42 0.058
73
MRB001 Marburg Hemorrhagic Fever 41 0.058
74
EBL001 Ebola Hemorrhagic Fever 40 0.058
75
LSS003 Lassa Fever 40 0.058
76
FMR004 Fumarase Deficiency 38 0.058
77
LKS001 Leukostasis 35 0.058
78
KKC001 Kikuchi Disease 35 0.058
79
ARG001 Argentine Hemorrhagic Fever 33 0.058
80
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 26 0.058
81
INS009 Insulin-Resistance Type B 22 0.058
82
P ATM067 Autoimmune Polyendocrinopathy Type 3 18 0.058
83
c ATM066 Autoimmune Polyendocrinopathy Type 4 14 0.058
84
P CLR023 Colorectal Cancer 97 0.041
85
P HPT023 Hepatocellular Carcinoma 92 0.041
86
P PRS040 Prostate Cancer 90 0.041
87
P PNC035 Pancreatic Cancer 87 0.041
88
CYS001 Cystic Fibrosis 83 0.041
89
P RNL014 Renal Cell Carcinoma 82 0.041
90
P SCH015 Schizophrenia 77 0.041
91
P OVR042 Ovarian Cancer 76 0.041
92
ULC004 Ulcerative Colitis 76 0.041
93
P LVR013 Liver Disease 75 0.041
94
INS024 Insulin-Like Growth Factor I 75 0.041
95
MYL009 Myelodysplastic Syndrome 73 0.041
96
CNG034 Congestive Heart Failure 72 0.041
97
P INF038 Influenza 72 0.041
98
SQM006 Squamous Cell Carcinoma 70 0.041
99
P LYM118 Lymphoma 69 0.041
100
SVR004 Severe Combined Immunodeficiency 69 0.041
101
c HPT001 Hepatitis C 68 0.041
102
KPS004 Kaposi Sarcoma 67 0.041
103
P MYL005 Myelofibrosis 67 0.041
104
P MNN013 Meningitis 67 0.041
105
P MYL006 Myeloid Leukemia 66 0.041
106
LSH001 Leishmaniasis 66 0.041
107
ATH003 Atherosclerosis 65 0.041
108
P KDN017 Kidney Cancer 65 0.041
109
c HPT016 Hepatitis B 64 0.041
110
P THL005 Thalassemia 64 0.041
111
CHD001 Chediak-Higashi Syndrome 64 0.041
112
DFC004 Deficiency Anemia 64 0.041
113
P TXP001 Toxoplasmosis 61 0.041
114
P ASP006 Aspergillosis 61 0.041
115
c ATM010 Autoimmune Hemolytic Anemia 60 0.041
116
c ACT075 Acute Myocardial Infarction 60 0.041
117
P PRT013 Portal Hypertension 60 0.041
118
CLT003 Colitis 60 0.041
119
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.041
120
DNG003 Dengue Disease 60 0.041
121
c SYS004 Systemic Mastocytosis 60 0.041
122
GST045 Gastroenteritis 59 0.041
123
P ENC018 Encephalopathy 59 0.041
124
P NRP001 Neuropathy 59 0.041
125
P ALC004 Alcohol Abuse 59 0.041
126
MYL031 Myeloproliferative Neoplasm 58 0.041
127
CHL071 Child Syndrome 58 0.041
128
ALP008 Alopecia 57 0.041
129
SVR066 Severe Combined Immunodeficiency, X-Linked 57 0.041
130
RTN017 Retinal Detachment 56 0.041
131
HRP004 Herpes Zoster 56 0.041
132
HYP266 Hypoxia 56 0.041
133
PRS047 Prostatitis 56 0.041
134
P FNC043 Fanconi Anemia, Complementation Group E 55 0.041
135
P HYP076 Hyperthyroidism 55 0.041
136
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.041
137
PLV003 Pelvic Inflammatory Disease 54 0.041
138
KDS001 Kid Syndrome 53 0.041
139
BLM002 Bulimia Nervosa 52 0.041
140
P PNC001 Pancytopenia 52 0.041
141
HMG005 Hemoglobinopathy 52 0.041
142
LYS003 Lysinuric Protein Intolerance 52 0.041
143
ISV001 Isovaleric Acidemia 51 0.041
144
ASP003 Aseptic Meningitis 51 0.041
145
MST005 Mastitis 51 0.041
146
BNM001 Bone Marrow Cancer 51 0.041
147
CRY005 Cryptococcosis 50 0.041
148
RTN023 Retinitis 50 0.041
149
PNM001 Pneumocystosis 50 0.041
150
DRG003 Drug Dependence 50 0.041
151
CSY001 C Syndrome 50 0.041
152
PLR001 Pleural Tuberculosis 49 0.041
153
HMG002 Hemoglobinuria 48 0.041
154
PSD007 Pseudomyxoma Peritonei 48 0.041
155
THL018 Thalassemia Major 48 0.041
156
CNG028 Congenital Hypoplastic Anemia 48 0.041
157
c CNG027 Congenital Hemolytic Anemia 48 0.041
158
DWR001 Dwarfism 47 0.041
159
LPM005 Lipomatosis 47 0.041
160
HMN032 Human Herpesvirus 8 46 0.041
161
P FNC044 Fanconi Anemia, Complementation Group C 46 0.041
162
BLD053 Blood Platelet Disease 46 0.041
163
INC022 Inclusion-Cell Disease 46 0.041
164
SPL012 Splenic Disease 46 0.041
165
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 45 0.041
166
MYL004 Myelodysplastic Myeloproliferative Cancer 45 0.041
167
P END047 Endophthalmitis 45 0.041
168
OST003 Osteonecrosis 45 0.041
169
GDS001 Good Syndrome 44 0.041
170
DYS164 Dyskeratosis Congenita, X-Linked 44 0.041
171
c FNC032 Fanconi Anemia, Complementation Group B 43 0.041
172
ANC002 Anca-Associated Vasculitis 42 0.041
173
c FNC045 Fanconi Anemia, Complementation Group F 42 0.041
174
c VRL005 Viral Pneumonia 42 0.041
175
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 41 0.041
176
c PRM023 Pre-Malignant Neoplasm 41 0.041
177
THL017 Thalassemia Intermedia 40 0.041
178
CHR078 Chorioretinitis 40 0.041
179
TLR001 Tularemia 39 0.041
180
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 39 0.041
181
c PRM225 Primary Thrombocytopenia 39 0.041
182
THL010 Thalassemia Minor 39 0.041
183
MNN021 Meningococcemia 39 0.041
184
SVR033 Severe Combined Immunodeficiency, B Cell-Negative 38 0.041
185
EHR002 Ehrlichiosis 38 0.041
186
OST115 Osteonecrosis of the Jaw 38 0.041
187
SHW001 Shwartzman Phenomenon 37 0.041
188
c FNC042 Fanconi Anemia, Complementation Group D2 37 0.041
189
SVR029 Severe Combined Immunodeficiency, T Cell-Negative, B-Cell/natural Killer-Cell Positive 36 0.041
190
SVR031 Severe Combined Immunodeficiency, Athabascan Type 36 0.041
191
NTR005 Nutritional Deficiency Disease 36 0.041
192
SPL011 Spleen Cancer 36 0.041
193
c THR037 Thrombocytopenia 2 35 0.041
194
SVR006 Severe Combined Immunodeficiency Due to Ada Deficiency 35 0.041
195
NTR006 Neutrophil Immunodeficiency Syndrome 35 0.041
196
TRP004 Tropical Sprue 35 0.041
197
TXC007 Toxic Pneumonitis 33 0.041
198
CHR463 Chronic Actinic Dermatitis 31 0.041
199
c FNC028 Fanconi Anemia, Complementation Group L 30 0.041
200
c VRL017 Viral Hemorrhagic Fever 30 0.041
201
CLR007 Colorado Tick Fever 29 0.041
202
MRG013 Mirage Syndrome 29 0.041
203
FNC030 Fanconi Anemia, Complementation Group G 29 0.041
204
c DMN018 Diamond-Blackfan Anemia 5 29 0.041
205
PRM243 Primary Bone Cancer 29 0.041
206
c FNC046 Fanconi Anemia, Complementation Group P 28 0.041
207
c FNC024 Fanconi Anemia, Complementation Group D1 28 0.041
208
FLT009 Folate Malabsorption, Hereditary 28 0.041
209
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 28 0.041
210
P KLZ004 Kala-Azar 1 28 0.041
211
c FNC023 Fanconi Anemia, Complementation Group N 28 0.041
212
DNG004 Dengue Fever, Protection Against 28 0.041
213
c FNC029 Fanconi Anemia, Complementation Group I 27 0.041
214
c DYS143 Dyskeratosis Congenita, Autosomal Dominant 2 27 0.041
215
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 26 0.041
216
PRX008 Paroxysmal Cold Hemoglobinuria 26 0.041
217
SVR032 Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation 25 0.041
218
c FNC025 Fanconi Anemia, Complementation Group J 25 0.041
219
EXF003 Exfoliative Dermatitis 25 0.041
220
BNM011 Bone Marrow Failure Syndrome 2 25 0.041
221
GHS004 Ghosal Hematodiaphyseal Syndrome 24 0.041
222
c DYS147 Dyskeratosis Congenita, Autosomal Dominant 3 24 0.041
223
c FNC047 Fanconi Anemia, Complementation Group Q 23 0.041
224
c FNC048 Fanconi Anemia, Complementation Group O 23 0.041
225
STN012 Sting-Associated Vasculopathy, Infantile-Onset 22 0.041
226
PLY112 Polyarteritis Nodosa, Childhood-Onset 21 0.041
227
SCD002 Scid, Autosomal Recessive, T-Negative/b-Positive Type 21 0.041
228
c FNC052 Fanconi Anemia, Complementation Group T 20 0.041
229
c THR110 Thrombocytopenia 6 20 0.041
230
ARG004 Argyria 20 0.041
231
c FNC055 Fanconi Anemia Complementation Group R 19 0.041
232
c FNC053 Fanconi Anemia Complementation Group V 15 0.041
233
CD4004 Cd4 Deficiency 14 0.041
234
P FNC054 Fanconi Anemia Complementation Group U 14 0.041
235
TYP004 Typhoidal Tularemia 11 0.041
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