Search results for leukopenia

235 hits were found for leukopenia

# Family MCID Name MIFTS Score
1
RTC002 Reticular Dysgenesis 53 5.033
2
PRP001 Propionic Acidemia 63 3.839
3
P NTR004 Neutropenia 60 3.432
4
MYL071 Myelolymphatic Insufficiency 10 3.183
5
c NTR045 Neutropenia, Chronic Familial 18 3.135
6
c NTR050 Neutropenia, Severe Congenital, 4, Autosomal Recessive 32 2.251
7
WHM001 Whim Syndrome 52 2.216
8
FLT011 Felty Syndrome 51 2.216
9
P THR014 Thrombocytopenia 65 0.342
10
P LKM002 Leukemia 75 0.150
11
NTR018 Neutrophilia, Hereditary 46 0.125
12
c SYS001 Systemic Lupus Erythematosus 86 0.117
13
P LNG032 Lung Cancer 99 0.110
14
CRH001 Crohn's Disease 80 0.110
15
P HPT021 Hepatitis 75 0.110
16
GRN017 Granulocytopenia 49 0.110
17
P ART022 Arthritis 77 0.102
18
P LPS004 Lupus Erythematosus 69 0.102
19
LKC003 Leukocyte Disease 34 0.102
20
P RHM011 Rheumatoid Arthritis 91 0.093
21
P PNM007 Pneumonia 70 0.093
22
c SML038 Small Cell Cancer of the Lung 67 0.093
23
c BLM008 Bulimia Nervosa 2 53 0.093
24
P INF037 Inflammatory Bowel Disease 52 0.093
25
P BRS047 Breast Cancer 100 0.083
26
VSC011 Vasculitis 66 0.083
27
ACQ007 Acquired Immunodeficiency Syndrome 65 0.083
28
VRL011 Viral Infectious Disease 64 0.083
29
GNG013 Gingivitis 64 0.083
30
BRN106 Burns 57 0.083
31
LYM027 Lymphopenia 56 0.083
32
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 36 0.083
33
P PLM037 Pulmonary Hypertension 79 0.072
34
P FNC027 Fanconi Anemia, Complementation Group a 78 0.072
35
APL001 Aplastic Anemia 74 0.072
36
P FML018 Familial Mediterranean Fever 73 0.072
37
BRC012 Brucellosis 71 0.072
38
P MYC084 Mycobacterium Tuberculosis 1 69 0.072
39
DRM006 Dermatitis 67 0.072
40
P LYM026 Lymphoblastic Leukemia 66 0.072
41
P ENC004 Encephalitis 66 0.072
42
P PNC044 Pancreatitis 64 0.072
43
P CMR001 Camurati-Engelmann Disease 62 0.072
44
PRP030 Purpura 61 0.072
45
MCS002 Mucositis 61 0.072
46
c ACT073 Acute Leukemia 61 0.072
47
TCK001 Tick-Borne Encephalitis 55 0.072
48
CHN016 Cohen Syndrome 48 0.072
49
P BCT020 Bacteremia 2 34 0.072
50
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.072
51
MLR004 Malaria 86 0.059
52
P MYC007 Myocardial Infarction 81 0.059
53
ALP046 Alport Syndrome, X-Linked 74 0.059
54
LVR012 Liver Cirrhosis 73 0.059
55
MLN008 Melanoma 72 0.059
56
HMN044 Human Immunodeficiency Virus Type 1 71 0.059
57
SRC014 Sarcoma 68 0.059
58
CHD001 Chediak-Higashi Syndrome 67 0.059
59
TYP007 Typhoid Fever 67 0.059
60
MXD005 Mixed Connective Tissue Disease 66 0.059
61
ISC004 Ischemia 66 0.059
62
P SRC025 Sarcoidosis 1 63 0.059
63
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.059
64
OST003 Osteonecrosis 63 0.059
65
P GRV001 Graves' Disease 62 0.059
66
P DRR001 Diarrhea 60 0.059
67
ALL026 Allergic Hypersensitivity Disease 59 0.059
68
P GRS003 Griscelli Syndrome 58 0.059
69
CRM001 Crimean-Congo Hemorrhagic Fever 58 0.059
70
c GCH015 Gaucher Disease, Type I 57 0.059
71
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 54 0.059
72
LYS003 Lysinuric Protein Intolerance 53 0.059
73
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.059
74
P ADM011 Adams-Oliver Syndrome 52 0.059
75
BBS001 Babesiosis 51 0.059
76
P CRV039 Cervicitis 49 0.059
77
ISV001 Isovaleric Acidemia 49 0.059
78
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 47 0.059
79
AGG002 Aggressive Systemic Mastocytosis 47 0.059
80
EBL001 Ebola Hemorrhagic Fever 45 0.059
81
LSS003 Lassa Fever 45 0.059
82
SPL018 Splenomegaly 45 0.059
83
MRG013 Mirage Syndrome 44 0.059
84
MRB001 Marburg Hemorrhagic Fever 43 0.059
85
DYS164 Dyskeratosis Congenita, X-Linked 40 0.059
86
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 40 0.059
87
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.059
88
LKS001 Leukostasis 39 0.059
89
c BLD140 Blood Group, I System 37 0.059
90
KKC001 Kikuchi Disease 37 0.059
91
FLT009 Folate Malabsorption, Hereditary 36 0.059
92
ARG001 Argentine Hemorrhagic Fever 34 0.059
93
TNP004 Tn Polyagglutination Syndrome 33 0.059
94
c HRM012 Hermansky-Pudlak Syndrome 9 32 0.059
95
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 29 0.059
96
c DYS143 Dyskeratosis Congenita, Autosomal Dominant 2 28 0.059
97
GHS005 Ghosal Hematodiaphyseal Dysplasia 28 0.059
98
STN012 Sting-Associated Vasculopathy, Infantile-Onset 26 0.059
99
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 25 0.059
100
c DYS147 Dyskeratosis Congenita, Autosomal Dominant 3 24 0.059
101
P ATM067 Autoimmune Polyendocrinopathy Type 3 22 0.059
102
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 22 0.059
103
c ATM066 Autoimmune Polyendocrinopathy Type 4 21 0.059
104
IMM169 Immunoerythromyeloid Hypoplasia 20 0.059
105
IMM140 Immunodeficiency 47 20 0.059
106
INS009 Insulin-Resistance Type B 20 0.059
107
BNM011 Bone Marrow Failure Syndrome 2 20 0.059
108
PNC121 Pancytopenia and Occlusive Vascular Disease 10 0.059
109
P CLR023 Colorectal Cancer 98 0.042
110
P HPT023 Hepatocellular Carcinoma 94 0.042
111
P PNC035 Pancreatic Cancer 89 0.042
112
P PRS040 Prostate Cancer 88 0.042
113
CYS001 Cystic Fibrosis 85 0.042
114
INS024 Insulin-Like Growth Factor I 83 0.042
115
P OVR042 Ovarian Cancer 82 0.042
116
c LKM061 Leukemia, Acute Myeloid 81 0.042
117
ULC004 Ulcerative Colitis 80 0.042
118
P NNN008 Noonan Syndrome 1 77 0.042
119
P INF038 Influenza 77 0.042
120
P LVR013 Liver Disease 76 0.042
121
P MYL005 Myelofibrosis 75 0.042
122
MYL009 Myelodysplastic Syndrome 75 0.042
123
SQM006 Squamous Cell Carcinoma 74 0.042
124
CNG034 Congestive Heart Failure 74 0.042
125
KPS004 Kaposi Sarcoma 73 0.042
126
c HPT001 Hepatitis C 73 0.042
127
P CRV035 Cervical Cancer 72 0.042
128
LSH001 Leishmaniasis 71 0.042
129
SVR004 Severe Combined Immunodeficiency 71 0.042
130
P MNN013 Meningitis 71 0.042
131
P LYM118 Lymphoma 71 0.042
132
P SCH015 Schizophrenia 71 0.042
133
c BTT014 Beta-Thalassemia 70 0.042
134
P MYL006 Myeloid Leukemia 69 0.042
135
c HPT016 Hepatitis B 68 0.042
136
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.042
137
BRS051 Breast Disease 67 0.042
138
ATM095 Autoimmune Disease 66 0.042
139
c DNG003 Dengue Disease 66 0.042
140
GST045 Gastroenteritis 65 0.042
141
P THL005 Thalassemia 65 0.042
142
P TXP001 Toxoplasmosis 65 0.042
143
P ASP006 Aspergillosis 65 0.042
144
SYS004 Systemic Mastocytosis 65 0.042
145
MYL031 Myeloproliferative Neoplasm 64 0.042
146
c ACT075 Acute Myocardial Infarction 64 0.042
147
CMB081 Combined Immunodeficiency, X-Linked 64 0.042
148
ACT119 Acute Promyelocytic Leukemia 64 0.042
149
SVR066 Severe Combined Immunodeficiency, X-Linked 63 0.042
150
P NRP001 Neuropathy 63 0.042
151
CLT003 Colitis 63 0.042
152
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.042
153
P ALC004 Alcohol Abuse 63 0.042
154
P HML002 Hemolytic Anemia 62 0.042
155
HYP266 Hypoxia 61 0.042
156
HRP004 Herpes Zoster 61 0.042
157
P PRT013 Portal Hypertension 59 0.042
158
PRS047 Prostatitis 59 0.042
159
RTN017 Retinal Detachment 59 0.042
160
P ENC018 Encephalopathy 58 0.042
161
c ANM038 Anemia, Autoimmune Hemolytic 56 0.042
162
MST005 Mastitis 56 0.042
163
P ALP008 Alopecia 56 0.042
164
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.042
165
PLV003 Pelvic Inflammatory Disease 56 0.042
166
P HYP076 Hyperthyroidism 56 0.042
167
P DNG005 Dengue Virus 56 0.042
168
PNM001 Pneumocystosis 55 0.042
169
PSD007 Pseudomyxoma Peritonei 54 0.042
170
ASP003 Aseptic Meningitis 54 0.042
171
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 54 0.042
172
CRY005 Cryptococcosis 54 0.042
173
HMG005 Hemoglobinopathy 53 0.042
174
P BLM007 Bulimia Nervosa 1 53 0.042
175
RTN023 Retinitis 52 0.042
176
HMG002 Hemoglobinuria 52 0.042
177
P FNC043 Fanconi Anemia, Complementation Group E 52 0.042
178
SCH012 Schizoaffective Disorder 51 0.042
179
DRG003 Drug Dependence 51 0.042
180
P END047 Endophthalmitis 51 0.042
181
P LPM005 Lipomatosis 50 0.042
182
PLR001 Pleural Tuberculosis 50 0.042
183
HMN032 Human Herpesvirus 8 50 0.042
184
PNC001 Pancytopenia 50 0.042
185
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.042
186
DWR001 Dwarfism 48 0.042
187
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 47 0.042
188
EHR002 Ehrlichiosis 45 0.042
189
BLD053 Blood Platelet Disease 45 0.042
190
P FNC044 Fanconi Anemia, Complementation Group C 45 0.042
191
SVR096 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative 44 0.042
192
TLR001 Tularemia 44 0.042
193
MNN021 Meningococcemia 43 0.042
194
ANC002 Anca-Associated Vasculitis 42 0.042
195
c FNC032 Fanconi Anemia, Complementation Group B 42 0.042
196
OST115 Osteonecrosis of the Jaw 41 0.042
197
CHR078 Chorioretinitis 41 0.042
198
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.042
199
SHW001 Shwartzman Phenomenon 40 0.042
200
HMN002 Human Granulocytic Anaplasmosis 40 0.042
201
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.042
202
SVR098 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Positive 39 0.042
203
SVR010 Severe Combined Immunodeficiency with Sensitivity to Ionizing Radiation 38 0.042
204
TRP004 Tropical Sprue 38 0.042
205
GDS001 Good Syndrome 37 0.042
206
c VRL017 Viral Hemorrhagic Fever 37 0.042
207
c FNC045 Fanconi Anemia, Complementation Group F 35 0.042
208
c CRN243 Carney Complex, Type 1 35 0.042
209
FMR004 Fumarase Deficiency 34 0.042
210
CHR463 Chronic Actinic Dermatitis 34 0.042
211
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 33 0.042
212
c FNC028 Fanconi Anemia, Complementation Group L 32 0.042
213
CLR007 Colorado Tick Fever 31 0.042
214
P KLZ004 Kala-Azar 1 31 0.042
215
PRX008 Paroxysmal Cold Hemoglobinuria 30 0.042
216
ATM052 Autoimmune Disease 1 30 0.042
217
FNC030 Fanconi Anemia, Complementation Group G 29 0.042
218
EXF003 Exfoliative Dermatitis 28 0.042
219
c FNC024 Fanconi Anemia, Complementation Group D1 28 0.042
220
c FNC023 Fanconi Anemia, Complementation Group N 27 0.042
221
SVR032 Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation 27 0.042
222
c FNC046 Fanconi Anemia, Complementation Group P 25 0.042
223
c FNC029 Fanconi Anemia, Complementation Group I 25 0.042
224
c FNC047 Fanconi Anemia, Complementation Group Q 24 0.042
225
c FNC048 Fanconi Anemia, Complementation Group O 22 0.042
226
MYL064 Myeloproliferative/lymphoproliferative Neoplasms, Familial 21 0.042
227
ARG004 Argyria 21 0.042
228
c FNC025 Fanconi Anemia, Complementation Group J 21 0.042
229
c DMN018 Diamond-Blackfan Anemia 5 21 0.042
230
c FNC057 Fanconi Anemia, Complementation Group U 21 0.042
231
c FNC058 Fanconi Anemia, Complementation Group R 20 0.042
232
c FNC052 Fanconi Anemia, Complementation Group T 20 0.042
233
c FNC056 Fanconi Anemia, Complementation Group V 20 0.042
234
c PSD047 Pseudo-Turner Syndrome 15 0.042
235
TYP004 Typhoidal Tularemia 12 0.042
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