Search results for leukopenia

228 hits were found for leukopenia

# Family MCID Name MIFTS Score
1
RTC002 Reticular Dysgenesis 51 5.155
2
PRP084 Propionicacidemia 57 3.211
3
P NTR004 Neutropenia 58 2.598
4
c NTR039 Neutropenia, Severe Congenital 4, Autosomal Recessive 32 2.332
5
WHM001 Whim Syndrome 52 2.271
6
FLT011 Felty Syndrome 46 2.271
7
c NTR008 Neutropenia Chronic Familial 16 2.271
8
P THR014 Thrombocytopenia 63 0.343
9
P LKM002 Leukemia 72 0.151
10
c SYS001 Systemic Lupus Erythematosus 86 0.126
11
P LNG032 Lung Cancer 94 0.111
12
CRH001 Crohn's Disease 73 0.111
13
P HPT021 Hepatitis 68 0.111
14
GRN017 Granulocytopenia 38 0.111
15
P ART022 Arthritis 72 0.103
16
P LPS004 Lupus Erythematosus 63 0.103
17
P RHM011 Rheumatoid Arthritis 87 0.094
18
P PNM007 Pneumonia 66 0.094
19
P INF037 Inflammatory Bowel Disease 62 0.094
20
P ANR007 Anorexia Nervosa 60 0.094
21
P BRS047 Breast Cancer 100 0.084
22
VSC011 Vasculitis 62 0.084
23
GNG013 Gingivitis 61 0.084
24
ACQ007 Acquired Immunodeficiency Syndrome 60 0.084
25
VRL011 Viral Infectious Disease 59 0.084
26
LYM027 Lymphopenia 54 0.084
27
BRN106 Burns 52 0.084
28
HMN014 Human Immunodeficiency Virus Infectious Disease 45 0.084
29
MTH039 Methylmalonic Aciduria, Mut(0) Type 35 0.084
30
P PLM037 Pulmonary Hypertension 77 0.073
31
P APL001 Aplastic Anemia 74 0.073
32
c FNC027 Fanconi Anemia, Complementation Group a 71 0.073
33
TBR010 Tuberculosis 69 0.073
34
DRM006 Dermatitis 63 0.073
35
P ENC004 Encephalitis 61 0.073
36
c ACT073 Acute Leukemia 61 0.073
37
P LYM026 Lymphoblastic Leukemia 60 0.073
38
P PNC044 Pancreatitis 60 0.073
39
P CMR001 Camurati-Engelmann Disease 59 0.073
40
PRP030 Purpura 57 0.073
41
CHN016 Cohen Syndrome 54 0.073
42
MCS002 Mucositis 54 0.073
43
BCT015 Bacteremia 47 0.073
44
TCK001 Tick-Borne Encephalitis 47 0.073
45
c DYS143 Dyskeratosis Congenita, Autosomal Dominant 2 30 0.073
46
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 28 0.073
47
MLR004 Malaria 82 0.059
48
HV1006 Hiv-1 80 0.059
49
P MYC007 Myocardial Infarction 77 0.059
50
P ALP004 Alport Syndrome 70 0.059
51
MLN008 Melanoma 70 0.059
52
LVR012 Liver Cirrhosis 66 0.059
53
SRC014 Sarcoma 66 0.059
54
CHD001 Chediak-Higashi Syndrome 65 0.059
55
HMT002 Hematologic Cancer 62 0.059
56
P SRC025 Sarcoidosis 1 61 0.059
57
P HML002 Hemolytic Anemia 61 0.059
58
MXD005 Mixed Connective Tissue Disease 61 0.059
59
ISC004 Ischemia 59 0.059
60
P DRR001 Diarrhea 59 0.059
61
ADL002 Adult Syndrome 57 0.059
62
P GRV001 Graves' Disease 57 0.059
63
CRM001 Crimean-Congo Hemorrhagic Fever 55 0.059
64
c GCH015 Gaucher Disease, Type I 54 0.059
65
P GRS003 Griscelli Syndrome 54 0.059
66
LYS003 Lysinuric Protein Intolerance 53 0.059
67
ISV001 Isovaleric Acidemia 51 0.059
68
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 51 0.059
69
P ADM011 Adams-Oliver Syndrome 50 0.059
70
BBS001 Babesiosis 47 0.059
71
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 46 0.059
72
LKC003 Leukocyte Disease 46 0.059
73
P CRV039 Cervicitis 45 0.059
74
SPL018 Splenomegaly 45 0.059
75
AGG002 Aggressive Systemic Mastocytosis 43 0.059
76
EBL001 Ebola Hemorrhagic Fever 43 0.059
77
DYS164 Dyskeratosis Congenita, X-Linked 42 0.059
78
LSS003 Lassa Fever 41 0.059
79
FMR004 Fumarase Deficiency 40 0.059
80
MRB001 Marburg Hemorrhagic Fever 40 0.059
81
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 38 0.059
82
LKS001 Leukostasis 35 0.059
83
KKC001 Kikuchi Disease 34 0.059
84
FLT009 Folate Malabsorption, Hereditary 32 0.059
85
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 30 0.059
86
INS009 Insulin-Resistance Type B 26 0.059
87
c DYS147 Dyskeratosis Congenita, Autosomal Dominant 3 26 0.059
88
PLY112 Polyarteritis Nodosa, Childhood-Onset 26 0.059
89
BNM011 Bone Marrow Failure Syndrome 2 26 0.059
90
STN012 Sting-Associated Vasculopathy, Infantile-Onset 26 0.059
91
GHS004 Ghosal Hematodiaphyseal Syndrome 25 0.059
92
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 24 0.059
93
P ATM067 Autoimmune Polyendocrinopathy Type 3 21 0.059
94
c ATM066 Autoimmune Polyendocrinopathy Type 4 17 0.059
95
TNP003 Tn Polyagglutination Syndrome, Somatic 15 0.059
96
P CLR023 Colorectal Cancer 95 0.042
97
P HPT023 Hepatocellular Carcinoma 89 0.042
98
P PRS040 Prostate Cancer 88 0.042
99
CYS001 Cystic Fibrosis 86 0.042
100
P PNC035 Pancreatic Cancer 84 0.042
101
P RNL014 Renal Cell Carcinoma 80 0.042
102
INS024 Insulin-Like Growth Factor I 75 0.042
103
P LVR013 Liver Disease 72 0.042
104
ULC004 Ulcerative Colitis 72 0.042
105
P SCH015 Schizophrenia 71 0.042
106
P INF038 Influenza 71 0.042
107
MYL009 Myelodysplastic Syndrome 71 0.042
108
CNG034 Congestive Heart Failure 70 0.042
109
SQM006 Squamous Cell Carcinoma 69 0.042
110
P LYM118 Lymphoma 69 0.042
111
SVR004 Severe Combined Immunodeficiency 69 0.042
112
KPS004 Kaposi Sarcoma 67 0.042
113
LSH001 Leishmaniasis 66 0.042
114
P MNN013 Meningitis 65 0.042
115
ATH003 Atherosclerosis 65 0.042
116
P MYL006 Myeloid Leukemia 64 0.042
117
c HPT001 Hepatitis C 62 0.042
118
c HPT016 Hepatitis B 62 0.042
119
P THL005 Thalassemia 61 0.042
120
TYP007 Typhoid Fever 61 0.042
121
P ASP006 Aspergillosis 60 0.042
122
DFC004 Deficiency Anemia 60 0.042
123
DNG003 Dengue Disease 60 0.042
124
SYS004 Systemic Mastocytosis 60 0.042
125
BRS051 Breast Disease 60 0.042
126
c ATM010 Autoimmune Hemolytic Anemia 60 0.042
127
P TXP001 Toxoplasmosis 60 0.042
128
CHL071 Child Syndrome 59 0.042
129
c ACT075 Acute Myocardial Infarction 59 0.042
130
P PRT013 Portal Hypertension 58 0.042
131
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 58 0.042
132
CLT003 Colitis 58 0.042
133
MYL031 Myeloproliferative Neoplasm 57 0.042
134
GST045 Gastroenteritis 57 0.042
135
P ALC004 Alcohol Abuse 57 0.042
136
P THR005 Thrombotic Thrombocytopenic Purpura 57 0.042
137
KDS001 Kid Syndrome 57 0.042
138
P NRP001 Neuropathy 57 0.042
139
SVR066 Severe Combined Immunodeficiency, X-Linked 57 0.042
140
HYP266 Hypoxia 55 0.042
141
PRS047 Prostatitis 55 0.042
142
HRP004 Herpes Zoster 54 0.042
143
ALP008 Alopecia 54 0.042
144
RTN017 Retinal Detachment 54 0.042
145
P HYP076 Hyperthyroidism 53 0.042
146
CSY001 C Syndrome 53 0.042
147
THL018 Thalassemia Major 52 0.042
148
P ENC018 Encephalopathy 52 0.042
149
PLV003 Pelvic Inflammatory Disease 51 0.042
150
P FNC043 Fanconi Anemia, Complementation Group E 51 0.042
151
HMG005 Hemoglobinopathy 51 0.042
152
BLM002 Bulimia Nervosa 51 0.042
153
CRY005 Cryptococcosis 50 0.042
154
MST005 Mastitis 50 0.042
155
ASP003 Aseptic Meningitis 50 0.042
156
PNC001 Pancytopenia 49 0.042
157
PSD007 Pseudomyxoma Peritonei 49 0.042
158
RTN023 Retinitis 49 0.042
159
DRG003 Drug Dependence 48 0.042
160
SCH012 Schizoaffective Disorder 48 0.042
161
c FNC042 Fanconi Anemia, Complementation Group D2 48 0.042
162
P LPM005 Lipomatosis 48 0.042
163
HMG002 Hemoglobinuria 48 0.042
164
P FNC044 Fanconi Anemia, Complementation Group C 47 0.042
165
PNM001 Pneumocystosis 47 0.042
166
BLD053 Blood Platelet Disease 46 0.042
167
SPL012 Splenic Disease 46 0.042
168
HMN032 Human Herpesvirus 8 46 0.042
169
GDS001 Good Syndrome 46 0.042
170
PLR001 Pleural Tuberculosis 46 0.042
171
P END047 Endophthalmitis 45 0.042
172
DWR001 Dwarfism 45 0.042
173
c FNC032 Fanconi Anemia, Complementation Group B 43 0.042
174
OST003 Osteonecrosis 43 0.042
175
ANC002 Anca-Associated Vasculitis 42 0.042
176
c PRM225 Primary Thrombocytopenia 42 0.042
177
c FNC045 Fanconi Anemia, Complementation Group F 42 0.042
178
TLR001 Tularemia 41 0.042
179
THL017 Thalassemia Intermedia 40 0.042
180
SVR033 Severe Combined Immunodeficiency, B Cell-Negative 39 0.042
181
EHR002 Ehrlichiosis 39 0.042
182
THL010 Thalassemia Minor 38 0.042
183
SVR031 Severe Combined Immunodeficiency, Athabascan Type 38 0.042
184
MNN021 Meningococcemia 38 0.042
185
OST115 Osteonecrosis of the Jaw 38 0.042
186
SVR006 Severe Combined Immunodeficiency Due to Ada Deficiency 37 0.042
187
c THR037 Thrombocytopenia 2 37 0.042
188
SHW001 Shwartzman Phenomenon 37 0.042
189
SVR029 Severe Combined Immunodeficiency, T Cell-Negative, B-Cell/natural Killer-Cell Positive 37 0.042
190
CHR078 Chorioretinitis 37 0.042
191
MRG013 Mirage Syndrome 36 0.042
192
BNS002 Bone Structure Disease 36 0.042
193
NTR006 Neutrophil Immunodeficiency Syndrome 35 0.042
194
c VRL017 Viral Hemorrhagic Fever 35 0.042
195
TRP004 Tropical Sprue 35 0.042
196
TXC007 Toxic Pneumonitis 34 0.042
197
c FNC028 Fanconi Anemia, Complementation Group L 32 0.042
198
c HRM012 Hermansky-Pudlak Syndrome 9 32 0.042
199
CHR463 Chronic Actinic Dermatitis 31 0.042
200
FNC030 Fanconi Anemia, Complementation Group G 30 0.042
201
c FNC046 Fanconi Anemia, Complementation Group P 30 0.042
202
c FNC024 Fanconi Anemia, Complementation Group D1 30 0.042
203
c DMN018 Diamond-Blackfan Anemia 5 30 0.042
204
ARG001 Argentine Hemorrhagic Fever 30 0.042
205
c FNC029 Fanconi Anemia, Complementation Group I 29 0.042
206
DNG004 Dengue Fever, Protection Against 28 0.042
207
c THR110 Thrombocytopenia 6 28 0.042
208
c FNC023 Fanconi Anemia, Complementation Group N 28 0.042
209
P KLZ004 Kala-Azar 1 28 0.042
210
PRX008 Paroxysmal Cold Hemoglobinuria 28 0.042
211
SCD002 Scid, Autosomal Recessive, T-Negative/b-Positive Type 27 0.042
212
SVR032 Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation 26 0.042
213
CLR007 Colorado Tick Fever 26 0.042
214
NLL002 Null Syndrome 26 0.042
215
c FNC025 Fanconi Anemia, Complementation Group J 25 0.042
216
EXF003 Exfoliative Dermatitis 25 0.042
217
c FNC048 Fanconi Anemia, Complementation Group O 24 0.042
218
P MYL064 Myeloproliferative/lymphoproliferative Neoplasms, Familial 24 0.042
219
c FNC047 Fanconi Anemia, Complementation Group Q 23 0.042
220
c FNC058 Fanconi Anemia, Complementation Group R 22 0.042
221
IMM140 Immunodeficiency 47 22 0.042
222
P FNC052 Fanconi Anemia, Complementation Group T 21 0.042
223
ARG004 Argyria 19 0.042
224
c FNC057 Fanconi Anemia, Complementation Group U 19 0.042
225
c FNC056 Fanconi Anemia, Complementation Group V 18 0.042
226
THR112 Thrombocytopenia, Anemia, and Myelofibrosis 18 0.042
227
CD4004 Cd4 Deficiency 17 0.042
228
TYP004 Typhoidal Tularemia 8 0.042
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