Search results for "leukopenia"

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

452 hits were found for 'leukopenia'

# Family MCID Name MIFTS Score
1
RTC002 Reticular Dysgenesis 46 4.539
2
PRP084 Propionicacidemia 55 3.906
3
P NTR004 Neutropenia 52 2.373
4
WHM001 Whim Syndrome 48 2.255
5
FLT001 Felty's Syndrome 45 2.255
6
c NTR039 Neutropenia, Severe Congenital 4, Autosomal Recessive 29 2.255
7
c NTR008 Neutropenia Chronic Familial 10 2.255
8
P LKM002 Leukemia 63 0.107
9
P LYM118 Lymphoma 57 0.102
10
P HPT021 Hepatitis 63 0.097
11
PRS047 Prostatitis 53 0.097
12
P BRS047 Breast Cancer 100 0.091
13
END072 Endotheliitis 41 0.085
14
LKC003 Leukocyte Disease 35 0.079
15
P PRS040 Prostate Cancer 87 0.072
16
P LNG032 Lung Cancer 91 0.064
17
c HPT001 Hepatitis C 65 0.064
18
c HPT073 Hepatitis C Virus 62 0.064
19
P AMY004 Amyloidosis 59 0.064
20
P MNN013 Meningitis 55 0.064
21
ACQ007 Acquired Immunodeficiency Syndrome 55 0.064
22
ADN018 Adenoma 53 0.064
23
CRB009 Cerebritis 44 0.064
24
HMN014 Human Immunodeficiency Virus Infectious Disease 39 0.064
25
HV1006 Hiv-1 78 0.056
26
P MYC007 Myocardial Infarction 77 0.056
27
c FNC027 Fanconi Anemia, Complementation Group a 66 0.056
28
SRC014 Sarcoma 61 0.056
29
P CMR001 Camurati-Engelmann Disease 58 0.056
30
P PNM007 Pneumonia 56 0.056
31
P LYM026 Lymphoblastic Leukemia 55 0.056
32
P PNC044 Pancreatitis 53 0.056
33
ISC004 Ischemia 49 0.056
34
TTR011 Tetraploidy 48 0.056
35
P NRP001 Neuropathy 47 0.056
36
P CNT005 Central Nervous System Lymphoma 45 0.056
37
GST053 Gastric Cancer 44 0.056
38
P ATX004 Ataxia 43 0.056
39
c PRM226 Primary Central Nervous System Lymphoma 42 0.056
40
NTR005 Nutritional Deficiency Disease 39 0.056
41
P CLR023 Colorectal Cancer 91 0.046
42
P OBS005 Obesity 87 0.046
43
P RHM011 Rheumatoid Arthritis 87 0.046
44
c SYS001 Systemic Lupus Erythematosus 84 0.046
45
P PLM037 Pulmonary Hypertension 78 0.046
46
P AST005 Asthma 77 0.046
47
P OVR042 Ovarian Cancer 69 0.046
48
PTZ001 Peutz-Jeghers Syndrome 68 0.046
49
P APL001 Aplastic Anemia 68 0.046
50
TBR010 Tuberculosis 65 0.046
51
P ART022 Arthritis 63 0.046
52
P MYL006 Myeloid Leukemia 61 0.046
53
LSH001 Leishmaniasis 61 0.046
54
PRT036 Peritonitis 59 0.046
55
P CRD011 Cardiomyopathy 59 0.046
56
P ADN016 Adenocarcinoma 59 0.046
57
TYP007 Typhoid Fever 58 0.046
58
c HPT016 Hepatitis B 57 0.046
59
SCH014 Schistosomiasis 57 0.046
60
ACN011 Acne 55 0.046
61
MXD005 Mixed Connective Tissue Disease 54 0.046
62
P ESP024 Esophagitis 54 0.046
63
P THR014 Thrombocytopenia 54 0.046
64
P ADM011 Adams-Oliver Syndrome 53 0.046
65
SPT005 Spotted Fever 53 0.046
66
CRM001 Crimean-Congo Hemorrhagic Fever 53 0.046
67
GNG013 Gingivitis 52 0.046
68
DMN002 Dementia 51 0.046
69
TYP011 Typhus 49 0.046
70
P THY032 Thyroiditis 49 0.046
71
VRL011 Viral Infectious Disease 48 0.046
72
VGN023 Vaginitis 47 0.046
73
ASP003 Aseptic Meningitis 47 0.046
74
c HPT003 Hepatitis a 47 0.046
75
c GCH015 Gaucher Disease, Type I 47 0.046
76
ANR040 Aneurysm 46 0.046
77
BBS001 Babesiosis 46 0.046
78
GNG012 Gingival Overgrowth 45 0.046
79
P ENC018 Encephalopathy 43 0.046
80
P OPH004 Ophthalmoplegia 42 0.046
81
P GRS003 Griscelli Syndrome 42 0.046
82
ALB002 Albinism 42 0.046
83
P CRV039 Cervicitis 41 0.046
84
AGG002 Aggressive Systemic Mastocytosis 41 0.046
85
c GCH017 Gaucher Disease, Type Iii 39 0.046
86
MRB001 Marburg Hemorrhagic Fever 39 0.046
87
BRN106 Burns 38 0.046
88
TRN012 Transient Global Amnesia 38 0.046
89
EBL001 Ebola Hemorrhagic Fever 37 0.046
90
LSS003 Lassa Fever 37 0.046
91
GLM008 Glomus Tumor 37 0.046
92
MNK002 Monkeypox 37 0.046
93
FMR004 Fumarase Deficiency 37 0.046
94
PST053 Postherpetic Neuralgia 32 0.046
95
SXL003 Sexual Disorder 32 0.046
96
IPX001 Ipex Syndrome 31 0.046
97
ARG001 Argentine Hemorrhagic Fever 31 0.046
98
MTH039 Methylmalonic Aciduria, Mut(0) Type 26 0.046
99
ADG002 Audiogenic Seizures 23 0.046
100
TNP003 Tn Polyagglutination Syndrome, Somatic 16 0.046
101
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 11 0.046
102
HPT023 Hepatocellular Carcinoma 87 0.032
103
P PNC035 Pancreatic Cancer 82 0.032
104
P RNL014 Renal Cell Carcinoma 81 0.032
105
P SCH015 Schizophrenia 76 0.032
106
MLR004 Malaria 75 0.032
107
P LFR001 Li-Fraumeni Syndrome 75 0.032
108
END057 Endometrial Cancer 73 0.032
109
HDG012 Hodgkin Lymphoma 73 0.032
110
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 0.032
111
CRH001 Crohn's Disease 71 0.032
112
P NRB001 Neuroblastoma 69 0.032
113
P LYN001 Lynch Syndrome 69 0.032
114
P INF038 Influenza 67 0.032
115
P LPR003 Leprosy 66 0.032
116
MYL009 Myelodysplastic Syndrome 65 0.032
117
P WSK001 Wiskott-Aldrich Syndrome 65 0.032
118
P CSH001 Cushing's Syndrome 64 0.032
119
P CLC005 Celiac Disease 63 0.032
120
CMM004 Common Variable Immunodeficiency 63 0.032
121
BRK010 Burkitt Lymphoma 63 0.032
122
P PLM036 Pulmonary Fibrosis 62 0.032
123
ANR002 Aniridia 62 0.032
124
P MYL005 Myelofibrosis 62 0.032
125
LSC001 Lesch-Nyhan Syndrome 61 0.032
126
P OST001 Osteopetrosis 61 0.032
127
CHD001 Chediak-Higashi Syndrome 60 0.032
128
OTT002 Otitis Media 60 0.032
129
ALC007 Alcohol Dependence 60 0.032
130
ART016 Aortic Aneurysm 60 0.032
131
CTN007 Cutaneous Leishmaniasis 59 0.032
132
P KDN017 Kidney Cancer 59 0.032
133
P LPS004 Lupus Erythematosus 59 0.032
134
P PRD006 Prader-Willi Syndrome 59 0.032
135
P PNC025 Panic Disorder 59 0.032
136
P BPL003 Bipolar Disorder 59 0.032
137
P ASP006 Aspergillosis 58 0.032
138
c HMP029 Hemophilia a 58 0.032
139
ATS001 Autistic Disorder 58 0.032
140
P TXP001 Toxoplasmosis 57 0.032
141
HMT002 Hematologic Cancer 57 0.032
142
DNG003 Dengue Disease 57 0.032
143
P DRM010 Dermatomyositis 57 0.032
144
P ORT004 Orthostatic Intolerance 57 0.032
145
P HMN010 Hemangioma 57 0.032
146
P HML002 Hemolytic Anemia 57 0.032
147
P GLB002 Glioblastoma 56 0.032
148
c HRD002 Hereditary Angioedema 56 0.032
149
P FRD001 Friedreich Ataxia 56 0.032
150
QFV001 Q Fever 56 0.032
151
ATH003 Atherosclerosis 56 0.032
152
FCT003 Factor X Deficiency 55 0.032
153
P NPH012 Nephrotic Syndrome 55 0.032
154
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 55 0.032
155
P HYP061 Hypertrophic Cardiomyopathy 55 0.032
156
P PRM002 Primary Hyperoxaluria 55 0.032
157
P THL005 Thalassemia 55 0.032
158
EPD016 Epidermolysis Bullosa 55 0.032
159
PLS007 Plasmodium Falciparum Malaria 55 0.032
160
P PRT010 Parathyroid Carcinoma 55 0.032
161
P CND004 Candidiasis 55 0.032
162
P SNS014 Sinusitis 55 0.032
163
MLN008 Melanoma 55 0.032
164
HRP004 Herpes Zoster 55 0.032
165
VSC003 Visceral Leishmaniasis 54 0.032
166
P THR015 Thrombophilia 54 0.032
167
P OST009 Osteochondritis Dissecans 54 0.032
168
P MSC005 Muscular Dystrophy 54 0.032
169
CHL123 Chlamydia 54 0.032
170
P INF032 Infertility 54 0.032
171
c SYS004 Systemic Mastocytosis 53 0.032
172
P RCK004 Rickets 53 0.032
173
P HMP002 Hemophagocytic Lymphohistiocytosis 53 0.032
174
P SJG001 Sjogren's Syndrome 53 0.032
175
PSD007 Pseudomyxoma Peritonei 53 0.032
176
P GRV001 Graves' Disease 53 0.032
177
P UVT001 Uveitis 53 0.032
178
c ACT027 Acute Pancreatitis 53 0.032
179
ISV001 Isovaleric Acidemia 52 0.032
180
P THR003 Thoracic Aortic Aneurysm 52 0.032
181
HRY003 Hairy Cell Leukemia 52 0.032
182
LYS003 Lysinuric Protein Intolerance 52 0.032
183
MLG056 Malignant Hyperthermia 52 0.032
184
HPY002 H. Pylori Infection 52 0.032
185
c ACT075 Acute Myocardial Infarction 51 0.032
186
STT001 Status Epilepticus 51 0.032
187
P DYS154 Dystonia 51 0.032
188
HPT019 Hepatic Encephalopathy 51 0.032
189
ORL015 Oral Squamous Cell Carcinoma 51 0.032
190
LNG099 Lung Disease 50 0.032
191
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 50 0.032
192
P ENC004 Encephalitis 50 0.032
193
P LRY019 Laryngitis 50 0.032
194
c FML108 Familial Breast Cancer 50 0.032
195
P HMP007 Hemophilia 50 0.032
196
GST040 Gastric Adenocarcinoma 50 0.032
197
P HMC002 Homocystinuria 50 0.032
198
P ANP001 Anaplastic Large Cell Lymphoma 50 0.032
199
P KDN018 Kidney Disease 49 0.032
200
MGL001 Megaloblastic Anemia 49 0.032
201
LPR001 Lepromatous Leprosy 49 0.032
202
P DGR001 Digeorge Syndrome 49 0.032
203
CRD137 Cardiogenic Shock 49 0.032
204
PPT005 Peptic Ulcer Disease 49 0.032
205
CMP002 Campylobacteriosis 49 0.032
206
c ACT073 Acute Leukemia 49 0.032
207
GTR002 Goiter 49 0.032
208
P PRS038 Personality Disorder 49 0.032
209
CRY005 Cryptococcosis 49 0.032
210
CST005 Castleman Disease 48 0.032
211
P GLL020 Gallbladder Disease 48 0.032
212
DFC004 Deficiency Anemia 48 0.032
213
ENT003 Enterobiasis 48 0.032
214
CHL069 Cholesteatoma 48 0.032
215
c THR082 Thrombophilia Due to Activated Protein C Resistance 48 0.032
216
BLR001 Biliary Atresia 48 0.032
217
THR004 Thrombocytosis 48 0.032
218
BRX001 Bruxism 48 0.032
219
ONC002 Onchocerciasis 47 0.032
220
P ANG015 Angioedema 47 0.032
221
INT002 Intermittent Claudication 47 0.032
222
CYT008 Cytomegalovirus Infection 47 0.032
223
GST033 Gestational Diabetes 47 0.032
224
P HYP065 Hyperaldosteronism 47 0.032
225
DPH001 Diphtheria 47 0.032
226
SRS001 Serous Cystadenocarcinoma 47 0.032
227
P NNT009 Neonatal Diabetes Mellitus 47 0.032
228
P HMR012 Hemorrhagic Fever 47 0.032
229
P CTR002 Cataract 47 0.032
230
LMB002 Lambert-Eaton Myasthenic Syndrome 47 0.032
231
PTN002 Patent Ductus Arteriosus 47 0.032
232
P HMN013 Hemangiopericytoma 47 0.032
233
CYS014 Cystadenocarcinoma 46 0.032
234
HNT002 Hantavirus Pulmonary Syndrome 46 0.032
235
CNS004 Constipation 46 0.032
236
UTR024 Uterine Carcinosarcoma 46 0.032
237
PTT006 Pituitary Adenoma 46 0.032
238
LPM004 Lipoma 46 0.032
239
P END033 Endocarditis 46 0.032
240
TMP001 Temporal Lobe Epilepsy 46 0.032
241
AVN001 Avian Influenza 46 0.032
242
BNM001 Bone Marrow Cancer 46 0.032
243
LYM022 Lymphangioma 46 0.032
244
c ALM001 Al Amyloidosis 46 0.032
245
EPD006 Epidermolysis Bullosa Acquisita 46 0.032
246
BRS051 Breast Disease 46 0.032
247
PLG002 Plague 46 0.032
248
URM002 Uremia 46 0.032
249
GST037 Gastroparesis 46 0.032
250
CHL071 Child Syndrome 45 0.032
251
HDC001 Headache 45 0.032
252
DCT002 Ductal Carcinoma in Situ 45 0.032
253
ART017 Aortic Disease 45 0.032
254
CLN003 Clonorchiasis 45 0.032
255
PPL002 Papillary Carcinoma 45 0.032
256
LYM009 Lymphocytic Choriomeningitis 45 0.032
257
P VSC005 Vesicoureteral Reflux 45 0.032
258
P PRK001 Porokeratosis 45 0.032
259
GST009 Gastroschisis 45 0.032
260
c INS002 in Situ Carcinoma 45 0.032
261
P HYP024 Hypoparathyroidism 45 0.032
262
CHN016 Cohen Syndrome 45 0.032
263
CHL068 Cholestasis 45 0.032
264
LYM040 Lymphoblastic Lymphoma 44 0.032
265
HYP099 Hyperferritinemia-Cataract Syndrome 44 0.032
266
P BRN009 Burning Mouth Syndrome 44 0.032
267
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 44 0.032
268
KDS001 Kid Syndrome 44 0.032
269
SBS003 Substance Abuse 44 0.032
270
OST011 Osteomalacia 44 0.032
271
P PLL002 Pellagra 44 0.032
272
P RNV001 Renovascular Hypertension 44 0.032
273
P STF001 Stiff-Person Syndrome 44 0.032
274
LYM027 Lymphopenia 44 0.032
275
P PRG013 Paraganglioma 44 0.032
276
P INT070 Intestinal Obstruction 44 0.032
277
ENH001 Enhanced S-Cone Syndrome 43 0.032
278
P FNC043 Fanconi Anemia, Complementation Group E 43 0.032
279
SPN051 Spondylitis 43 0.032
280
VCC001 Vaccinia 43 0.032
281
P MLT074 Multiple Endocrine Neoplasia 43 0.032
282
PRS045 Prostatic Hypertrophy 43 0.032
283
BRN071 Brain Injury 43 0.032
284
VRC001 Varicocele 43 0.032
285
P MLG086 Malignant Hyperthermia Susceptibility 43 0.032
286
NRN004 Neuroendocrine Tumor 43 0.032
287
OCL001 Ocular Albinism 42 0.032
288
PNM001 Pneumocystosis 42 0.032
289
ANG054 Angina Pectoris 42 0.032
290
CRC006 Carcinoid Syndrome 42 0.032
291
P SCK005 Sickle Cell Disease 42 0.032
292
P GRN010 Granular Cell Tumor 42 0.032
293
HMG005 Hemoglobinopathy 42 0.032
294
c INV001 Invasive Aspergillosis 42 0.032
295
CNG028 Congenital Hypoplastic Anemia 42 0.032
296
ADL002 Adult Syndrome 42 0.032
297
ANR004 Anuria 42 0.032
298
HLL004 Hellp Syndrome 42 0.032
299
P PRT029 Parathyroid Adenoma 41 0.032
300
KLD001 Keloids 41 0.032
301
CRB086 Cerebral Aneurysms 41 0.032
302
FBR054 Fibroma 41 0.032
303
FSC004 Fasciitis 41 0.032
304
MYL004 Myelodysplastic Myeloproliferative Cancer 41 0.032
305
OCL006 Ocular Hypertension 41 0.032
306
RCK002 Rocky Mountain Spotted Fever 41 0.032
307
NDL013 Nodular Regenerative Hyperplasia 41 0.032
308
CHR031 Chromoblastomycosis 41 0.032
309
c ACT134 Acute Liver Failure 41 0.032
310
c CHR092 Chronic Myeloproliferative Disease 40 0.032
311
VLV044 Vulvar Intraepithelial Neoplasia 40 0.032
312
RNL015 Renal Hypertension 40 0.032
313
HPT014 Hepatorenal Syndrome 40 0.032
314
ANG016 Angiokeratoma 40 0.032
315
AGR002 Agoraphobia 40 0.032
316
FCT001 Factor Viii Deficiency 40 0.032
317
KMR001 Kimura Disease 40 0.032
318
c CNG027 Congenital Hemolytic Anemia 39 0.032
319
LYM052 Lymphomatoid Papulosis 39 0.032
320
CSY001 C Syndrome 39 0.032
321
GRW007 Growth Hormone Deficiency 39 0.032
322
SPN041 Spinal Cord Disease 39 0.032
323
c SVR056 Severe Hemophilia a 39 0.032
324
ART035 Arterial Calcification of Infancy 39 0.032
325
c FNC032 Fanconi Anemia, Complementation Group B 39 0.032
326
DDN006 Duodenitis 39 0.032
327
P TCL004 T-Cell Leukemia 39 0.032
328
APR001 Apraxia 38 0.032
329
THR035 Thrombasthenia 38 0.032
330
VLV042 Vulvar Vestibulitis Syndrome 38 0.032
331
NRS003 Neurosyphilis 38 0.032
332
P VNS003 Venous Insufficiency 38 0.032
333
ANV001 Anovulation 38 0.032
334
P FNC044 Fanconi Anemia, Complementation Group C 38 0.032
335
DBT002 Diabetic Autonomic Neuropathy 38 0.032
336
CRV043 Cervical Dystonia 37 0.032
337
FBR009 Fibrous Dysplasia 37 0.032
338
P FNC052 Fanconi Anemia, Complementation Group T 37 0.032
339
KRN001 Korean Hemorrhagic Fever 37 0.032
340
ATN004 Autonomic Neuropathy 37 0.032
341
SPN029 Spondylolysis 37 0.032
342
VGN020 Vaginal Disease 37 0.032
343
RFR010 Refractory Anemia 37 0.032
344
ALL014 Allergic Encephalomyelitis 37 0.032
345
ASP007 Aspiration Pneumonia 37 0.032
346
P TST026 Testicular Germ Cell Cancer 36 0.032
347
SCL017 Sclerosing Hemangioma 36 0.032
348
BWN003 Bowenoid Papulosis 36 0.032
349
c THR090 Thrombocythemia 1 36 0.032
350
c FNC045 Fanconi Anemia, Complementation Group F 36 0.032
351
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 36 0.032
352
NRN002 Neuronitis 36 0.032
353
NDL007 Nodular Goiter 35 0.032
354
P SPR013 Spiradenoma 35 0.032
355
SVR066 Severe Combined Immunodeficiency, X-Linked 35 0.032
356
BRS090 Breast Reconstruction 35 0.032
357
BLD053 Blood Platelet Disease 35 0.032
358
c VRL005 Viral Pneumonia 34 0.032
359
ANX004 Anoxia 34 0.032
360
CHR466 Chronic Thromboembolic Pulmonary Hypertension 34 0.032
361
c PRM023 Pre-Malignant Neoplasm 34 0.032
362
SPL012 Splenic Disease 34 0.032
363
c RCR022 Recurrent Acute Pancreatitis 34 0.032
364
SVR029 Severe Combined Immunodeficiency, T Cell-Negative, B-Cell/natural Killer-Cell Positive 34 0.032
365
ACT087 Acth Deficiency 34 0.032
366
c MLT010 Multiple Personality Disorder 34 0.032
367
c RCR002 Recurrent Hypersomnia 33 0.032
368
ERY017 Erythema Elevatum Diutinum 33 0.032
369
LTH001 Lethal Midline Granuloma 33 0.032
370
DYS164 Dyskeratosis Congenita, X-Linked 33 0.032
371
WBR001 Weber Syndrome 33 0.032
372
TNC003 Tinea Corporis 32 0.032
373
GRN017 Granulocytopenia 32 0.032
374
c DYS143 Dyskeratosis Congenita, Autosomal Dominant 2 32 0.032
375
NCR007 Necrotizing Fasciitis 32 0.032
376
TXC007 Toxic Pneumonitis 32 0.032
377
MDS022 Mediastinitis 32 0.032
378
P HYP263 Hypersomnia 32 0.032
379
SKL007 Skeletal Muscle Regeneration 32 0.032
380
ALC011 Alcoholic Neuropathy 31 0.032
381
SPN221 Spina Bifida Occulta 31 0.032
382
c FML156 Familial Hyperaldosteronism 31 0.032
383
c FNC025 Fanconi Anemia, Complementation Group J 31 0.032
384
CRB004 Cerebral Artery Occlusion 31 0.032
385
FLT009 Folate Malabsorption, Hereditary 31 0.032
386
c PRM046 Primary Malignant Lymphoma 31 0.032
387
c FNC042 Fanconi Anemia, Complementation Group D2 31 0.032
388
MNN032 Meningococcal Meningitis 30 0.032
389
P SLP003 Salpingitis 30 0.032
390
THL010 Thalassemia Minor 30 0.032
391
FTL007 Fetal Hydantoin Syndrome 30 0.032
392
SVR006 Severe Combined Immunodeficiency Due to Ada Deficiency 30 0.032
393
P GGN002 Gigantism 30 0.032
394
MYB001 Myoblastoma 29 0.032
395
CNG069 Congenital Cytomegalovirus 28 0.032
396
c FNC028 Fanconi Anemia, Complementation Group L 28 0.032
397
PRS037 Periostitis 28 0.032
398
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 28 0.032
399
CHR028 Chronic Wasting Disease 28 0.032
400
c THR037 Thrombocytopenia 2 28 0.032
401
c PRM032 Primary Congenital Glaucoma 27 0.032
402
LNR004 Linear Porokeratosis 27 0.032
403
BNS002 Bone Structure Disease 27 0.032
404
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 27 0.032
405
CHN053 Chondromyxoid Fibroma 27 0.032
406
OLF002 Olfactory Groove Meningioma 27 0.032
407
c FNC029 Fanconi Anemia, Complementation Group I 26 0.032
408
SPL011 Spleen Cancer 26 0.032
409
OPT001 Optic Disk Drusen 26 0.032
410
HYP008 Hypertensive Retinopathy 26 0.032
411
SVR033 Severe Combined Immunodeficiency, B Cell-Negative 25 0.032
412
LYM002 Lymphoplasmacyte-Rich Meningioma 25 0.032
413
FNC030 Fanconi Anemia, Complementation Group G 25 0.032
414
GHS004 Ghosal Hematodiaphyseal Syndrome 25 0.032
415
EPT003 Epithelioid Trophoblastic Tumor 25 0.032
416
RFL002 Reflex Epilepsy 25 0.032
417
P PLM064 Pulmonary Sequestration 25 0.032
418
PLM007 Pulmonary Aspergilloma 25 0.032
419
c DYS147 Dyskeratosis Congenita, Autosomal Dominant 3 25 0.032
420
SVR031 Severe Combined Immunodeficiency, Athabascan Type 24 0.032
421
c VRL017 Viral Hemorrhagic Fever 24 0.032
422
c FNC047 Fanconi Anemia, Complementation Group Q 24 0.032
423
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 24 0.032
424
c FNC046 Fanconi Anemia, Complementation Group P 24 0.032
425
c FNC023 Fanconi Anemia, Complementation Group N 24 0.032
426
SCD002 Scid, Autosomal Recessive, T-Negative/b-Positive Type 24 0.032
427
c FNC048 Fanconi Anemia, Complementation Group O 23 0.032
428
c DMN018 Diamond-Blackfan Anemia 5 23 0.032
429
c FNC024 Fanconi Anemia, Complementation Group D1 23 0.032
430
SVR032 Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation 23 0.032
431
NRS005 Neurosarcoidosis 23 0.032
432
c PRM150 Primary Localized Amyloidosis 22 0.032
433
NTR006 Neutrophil Immunodeficiency Syndrome 22 0.032
434
IMM053 Immunotactoid Glomerulopathy 22 0.032
435
PLY112 Polyarteritis Nodosa, Childhood-Onset 21 0.032
436
STR029 Sternal Cleft 20 0.032
437
BNM011 Bone Marrow Failure Syndrome 2 20 0.032
438
CRN004 Corneal Abscess 19 0.032
439
STN012 Sting-Associated Vasculopathy, Infantile-Onset 19 0.032
440
ESP040 Esophageal Duplication Cyst 19 0.032
441
c THR087 Thrombocythemia 2 19 0.032
442
TRN046 Transverse Vaginal Septum 19 0.032
443
SCL008 Scleromalacia Perforans 18 0.032
444
PST037 Pasteurella Multocida Infection 18 0.032
445
CVR008 Cavernous Lymphangioma 17 0.032
446
VTM025 Vitamin B12-Unresponsive Methylmalonic Acidemia 17 0.032
447
SBN003 Subungual Glomus Tumor 16 0.032
448
FTL058 Fetal Trimethadione Syndrome 15 0.032
449
FLN005 Folinic Acid-Responsive Seizures 13 0.032
450
ACH028 Acheiria 13 0.032
451
DNG004 Dengue Fever, Protection Against 12 0.032
452
CD4004 Cd4 Deficiency 9 0.032