Search results for "hematopoiesis"

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

427 hits were found for 'hematopoiesis'

# Family MCID Name MIFTS Score
1
NTR040 Neutropenia, Cyclic 44 5.762
2
PRS047 Prostatitis 53 0.105
3
P PRS040 Prostate Cancer 87 0.100
4
END072 Endotheliitis 41 0.100
5
P LKM002 Leukemia 63 0.090
6
P ADN016 Adenocarcinoma 59 0.084
7
P OVR042 Ovarian Cancer 69 0.078
8
MLN008 Melanoma 55 0.078
9
P LYM118 Lymphoma 57 0.071
10
RTN023 Retinitis 42 0.071
11
P RNL014 Renal Cell Carcinoma 81 0.063
12
P ART022 Arthritis 63 0.063
13
SRC014 Sarcoma 61 0.063
14
P LVR013 Liver Disease 60 0.063
15
PRT036 Peritonitis 59 0.063
16
ADN018 Adenoma 53 0.063
17
P PNC044 Pancreatitis 53 0.063
18
P HMP007 Hemophilia 50 0.063
19
P THY032 Thyroiditis 49 0.063
20
P GLM045 Glioma 46 0.063
21
HYP266 Hypoxia 46 0.063
22
P CLR023 Colorectal Cancer 91 0.055
23
P OBS005 Obesity 87 0.055
24
HV1006 Hiv-1 78 0.055
25
P AST005 Asthma 77 0.055
26
P SCH015 Schizophrenia 76 0.055
27
P OST002 Osteoporosis 76 0.055
28
P OST012 Osteoarthritis 72 0.055
29
P NRB001 Neuroblastoma 69 0.055
30
P ESP024 Esophagitis 54 0.055
31
NSP002 Nasopharyngitis 48 0.055
32
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 44 0.055
33
P CRV039 Cervicitis 41 0.055
34
URT001 Urethritis 37 0.055
35
MDS022 Mediastinitis 32 0.055
36
P LNG032 Lung Cancer 91 0.045
37
P RHM011 Rheumatoid Arthritis 87 0.045
38
CYS001 Cystic Fibrosis 84 0.045
39
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 0.045
40
P RTT002 Rett Syndrome 71 0.045
41
FBR012 Fabry Disease 67 0.045
42
INS024 Insulin-Like Growth Factor I 67 0.045
43
MYL009 Myelodysplastic Syndrome 65 0.045
44
LSH001 Leishmaniasis 61 0.045
45
P CRD011 Cardiomyopathy 59 0.045
46
HMT002 Hematologic Cancer 57 0.045
47
P HMN010 Hemangioma 57 0.045
48
SCH014 Schistosomiasis 57 0.045
49
c HMP004 Hemophilia B 57 0.045
50
PRC002 Paracoccidioidomycosis 56 0.045
51
P CND004 Candidiasis 55 0.045
52
HRP004 Herpes Zoster 55 0.045
53
VSC003 Visceral Leishmaniasis 54 0.045
54
GNG013 Gingivitis 52 0.045
55
P RHN004 Rhinitis 52 0.045
56
MLG056 Malignant Hyperthermia 52 0.045
57
P ESN007 Eosinophilia 52 0.045
58
DMN002 Dementia 51 0.045
59
LYM021 Lymphadenitis 51 0.045
60
P GLM007 Glomerulonephritis 50 0.045
61
P LRY019 Laryngitis 50 0.045
62
P CMP010 Complex Regional Pain Syndrome 50 0.045
63
TRG002 Trigeminal Neuralgia 50 0.045
64
P KDN018 Kidney Disease 49 0.045
65
ISC004 Ischemia 49 0.045
66
c PRC016 Pre-Eclampsia 48 0.045
67
CND002 Conduct Disorder 47 0.045
68
P ECL001 Eclampsia 47 0.045
69
c PST041 Posterior Urethral Valves 47 0.045
70
PTT006 Pituitary Adenoma 46 0.045
71
RTN017 Retinal Detachment 46 0.045
72
ANR040 Aneurysm 46 0.045
73
P LTR001 Lateral Sclerosis 45 0.045
74
NWC001 Newcastle Disease 45 0.045
75
CRB009 Cerebritis 44 0.045
76
NRM005 Neuromuscular Disease 44 0.045
77
PPL021 Papilledema 43 0.045
78
P EXP004 Exophthalmos 42 0.045
79
HMG002 Hemoglobinuria 40 0.045
80
MLT018 Multiple Carboxylase Deficiency 35 0.045
81
P OVR046 Ovarian Cyst 35 0.045
82
c NTR033 Neutropenia, Severe Congenital 1, Autosomal Dominant 24 0.045
83
P BRS047 Breast Cancer 100 0.032
84
P PNC035 Pancreatic Cancer 82 0.032
85
P RTN008 Retinitis Pigmentosa 75 0.032
86
P ATX030 Ataxia-Telangiectasia 74 0.032
87
END057 Endometrial Cancer 73 0.032
88
P RTN024 Retinoblastoma 73 0.032
89
ULC004 Ulcerative Colitis 70 0.032
90
P PHC003 Pheochromocytoma 70 0.032
91
c CHR090 Chronic Lymphocytic Leukemia 69 0.032
92
P CRN211 Coronary Artery Disease 69 0.032
93
PHN003 Phenylketonuria 68 0.032
94
P OST005 Osteogenesis Imperfecta 67 0.032
95
P INF038 Influenza 67 0.032
96
CDS001 Cadasil 66 0.032
97
TBR010 Tuberculosis 65 0.032
98
MNT001 Mantle Cell Lymphoma 65 0.032
99
THY028 Thyroid Cancer 65 0.032
100
ATT013 Attention Deficit-Hyperactivity Disorder 65 0.032
101
c CNG401 Congenital Heart Disease 64 0.032
102
P NJM001 Nijmegen Breakage Syndrome 64 0.032
103
ALL003 Allergic Rhinitis 64 0.032
104
CNG034 Congestive Heart Failure 64 0.032
105
P HPT021 Hepatitis 63 0.032
106
KWS002 Kawasaki Disease 63 0.032
107
CHR012 Chronic Granulomatous Disease 62 0.032
108
P PLM036 Pulmonary Fibrosis 62 0.032
109
P MYL005 Myelofibrosis 62 0.032
110
P MYL006 Myeloid Leukemia 61 0.032
111
ALC007 Alcohol Dependence 60 0.032
112
PLY125 Polycythemia Vera, Somatic 60 0.032
113
P TBR001 Tuberous Sclerosis 60 0.032
114
P HRP006 Herpes Simplex 59 0.032
115
P AGM001 Agammaglobulinemia 59 0.032
116
c BSL007 Basal Cell Carcinoma 59 0.032
117
NRR002 Norrie Disease 59 0.032
118
c ATM003 Autoimmune Thyroiditis 59 0.032
119
P DYS007 Dyskeratosis Congenita 59 0.032
120
P CHR071 Charcot-Marie-Tooth Disease 58 0.032
121
P ASP006 Aspergillosis 58 0.032
122
P HRT032 Heart Disease 58 0.032
123
c HMP029 Hemophilia a 58 0.032
124
ATP002 Atopy 58 0.032
125
DWN001 Down Syndrome 58 0.032
126
P HYD006 Hydrocephalus 58 0.032
127
P BRG001 Brugada Syndrome 57 0.032
128
ART005 Arteriovenous Malformation 57 0.032
129
P AST007 Astrocytoma 57 0.032
130
P SDD001 Sudden Infant Death Syndrome 57 0.032
131
LVR012 Liver Cirrhosis 57 0.032
132
MSL001 Measles 57 0.032
133
P HML002 Hemolytic Anemia 57 0.032
134
P PNM007 Pneumonia 56 0.032
135
P EHL001 Ehlers-Danlos Syndrome 56 0.032
136
ATH003 Atherosclerosis 56 0.032
137
PMS001 Poems Syndrome 55 0.032
138
P MNN013 Meningitis 55 0.032
139
P HYP061 Hypertrophic Cardiomyopathy 55 0.032
140
ACN011 Acne 55 0.032
141
DRM006 Dermatitis 55 0.032
142
VSC007 Vascular Disease 55 0.032
143
EPD016 Epidermolysis Bullosa 55 0.032
144
PGT001 Paget's Disease of Bone 55 0.032
145
SHG001 Shigellosis 55 0.032
146
CRB039 Cerebrovascular Disease 55 0.032
147
P CHN012 Chondrosarcoma 54 0.032
148
WLL001 Williams-Beuren Syndrome 54 0.032
149
P JNC001 Junctional Epidermolysis Bullosa 54 0.032
150
P MCP010 Mucopolysaccharidosis 54 0.032
151
FTT001 Fatty Liver Disease 53 0.032
152
P PLY014 Polycystic Kidney Disease 53 0.032
153
CHR072 Chordoma 53 0.032
154
ALL006 Allergic Asthma 53 0.032
155
TNG003 Tongue Cancer 53 0.032
156
P GRV001 Graves' Disease 53 0.032
157
SPT005 Spotted Fever 53 0.032
158
CHR003 Cherubism 53 0.032
159
c ACT027 Acute Pancreatitis 53 0.032
160
HYP066 Hyperglycemia 53 0.032
161
P NSP012 Nasopharyngeal Carcinoma 53 0.032
162
CRY002 Cryptorchidism 53 0.032
163
CYS010 Cystinosis 53 0.032
164
P CRB042 Cerebellar Ataxia 52 0.032
165
RBS001 Rabies 52 0.032
166
P ALC004 Alcohol Abuse 52 0.032
167
HRY003 Hairy Cell Leukemia 52 0.032
168
PTY003 Pityriasis Rubra Pilaris 52 0.032
169
c SVR001 Severe Acute Respiratory Syndrome 52 0.032
170
P VNT002 Ventricular Septal Defect 51 0.032
171
P HYP086 Hypothyroidism 51 0.032
172
PLS011 Plasmacytoma 51 0.032
173
PLM033 Pulmonary Embolism 51 0.032
174
OBS061 Obstructive Sleep Apnea 51 0.032
175
BRN002 Bronchiolitis 51 0.032
176
URT039 Urticaria 51 0.032
177
RHM027 Rheumatic Disease 51 0.032
178
ACH005 Achalasia 50 0.032
179
ALL008 Allergic Bronchopulmonary Aspergillosis 50 0.032
180
VGT001 Vogt-Koyanagi-Harada Disease 50 0.032
181
P ENC004 Encephalitis 50 0.032
182
EMB004 Embryonal Carcinoma 50 0.032
183
END041 Endometrial Adenocarcinoma 50 0.032
184
P PLY017 Polyarteritis Nodosa 50 0.032
185
GST040 Gastric Adenocarcinoma 50 0.032
186
BRT005 Barth Syndrome 49 0.032
187
P TMT001 Timothy Syndrome 49 0.032
188
CRN036 Craniopharyngioma 49 0.032
189
P HYP076 Hyperthyroidism 49 0.032
190
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 49 0.032
191
CLT003 Colitis 49 0.032
192
SML019 Smallpox 49 0.032
193
P SML001 Small Cell Carcinoma 49 0.032
194
P TRT010 Teratoma 49 0.032
195
IDP002 Idiopathic Juvenile Osteoporosis 49 0.032
196
c ACT073 Acute Leukemia 49 0.032
197
RSC001 Rosacea 49 0.032
198
ART111 Artery Disease 49 0.032
199
c VRL007 Viral Encephalitis 49 0.032
200
MGK001 Megakaryocytic Leukemia 48 0.032
201
P GLL020 Gallbladder Disease 48 0.032
202
VSC002 Vascular Dementia 48 0.032
203
CLR003 Clear Cell Adenocarcinoma 48 0.032
204
P MYP006 Myopia 48 0.032
205
GSG001 Gas Gangrene 48 0.032
206
P CPL006 Capillary Hemangioma 48 0.032
207
CNN005 Connective Tissue Disease 48 0.032
208
P EXN002 Exanthem 48 0.032
209
P OPN001 Open-Angle Glaucoma 48 0.032
210
EXF001 Exfoliation Syndrome 48 0.032
211
ANG020 Angiosarcoma 48 0.032
212
BNC003 Bone Cancer 47 0.032
213
c MLG077 Malignant Peripheral Nerve Sheath Tumor 47 0.032
214
ONC002 Onchocerciasis 47 0.032
215
P HML001 Hemolytic-Uremic Syndrome 47 0.032
216
NRT004 Neuritis 47 0.032
217
ART031 Aortic Coarctation 47 0.032
218
P CTR002 Cataract 47 0.032
219
MCP006 Mucoepidermoid Carcinoma 47 0.032
220
LMB002 Lambert-Eaton Myasthenic Syndrome 47 0.032
221
JCB001 Jacobsen Syndrome 47 0.032
222
P NRP001 Neuropathy 47 0.032
223
P SLP006 Sleep Apnea 47 0.032
224
OMP004 Omphalocele 47 0.032
225
P CLR030 Clear Cell Renal Cell Carcinoma 46 0.032
226
PLV003 Pelvic Inflammatory Disease 46 0.032
227
AVN001 Avian Influenza 46 0.032
228
GLS001 Gliosarcoma 46 0.032
229
BNM001 Bone Marrow Cancer 46 0.032
230
SPN019 Spondylolisthesis 46 0.032
231
TRD006 Tardive Dyskinesia 46 0.032
232
SPR010 Sporotrichosis 45 0.032
233
MGC001 Megacolon 45 0.032
234
P DRR001 Diarrhea 45 0.032
235
PTH002 Pathological Gambling 45 0.032
236
P VSC005 Vesicoureteral Reflux 45 0.032
237
OCL009 Ocular Cancer 45 0.032
238
PRT011 Protein C Deficiency 45 0.032
239
STM007 Stomatitis 45 0.032
240
CRN017 Coronary Thrombosis 45 0.032
241
NTH001 Netherton Syndrome 45 0.032
242
PMP001 Pemphigus 45 0.032
243
DRC001 Dracunculiasis 45 0.032
244
SPN020 Spondylosis 45 0.032
245
INT075 Intracranial Hypertension 45 0.032
246
DRG011 Drug Addiction 45 0.032
247
c MLG068 Malignant Glioma 44 0.032
248
KRT009 Keratosis 44 0.032
249
SNS001 Sensorineural Hearing Loss 44 0.032
250
CLF001 Cleft Lip 44 0.032
251
URN003 Urinary Schistosomiasis 44 0.032
252
P PYL005 Pyelonephritis 44 0.032
253
LNN001 Lennox-Gastaut Syndrome 44 0.032
254
OST011 Osteomalacia 44 0.032
255
MCR088 Microscopic Polyangiitis 44 0.032
256
GST053 Gastric Cancer 44 0.032
257
NRG002 Neurogenic Bladder 44 0.032
258
P FNC004 Fanconi Syndrome 44 0.032
259
AMB001 Amebiasis 44 0.032
260
TRC023 Trichinosis 44 0.032
261
c TCL005 T-Cell Prolymphocytic Leukemia 44 0.032
262
P TRM004 Trimethylaminuria 43 0.032
263
CTS002 Cat-Scratch Disease 43 0.032
264
ORL005 Oral Candidiasis 43 0.032
265
TPT001 Tauopathy 43 0.032
266
P ATX004 Ataxia 43 0.032
267
TTH006 Tooth Disease 43 0.032
268
OPT009 Optic Neuritis 43 0.032
269
CRN014 Cronkhite-Canada Syndrome 43 0.032
270
BRN071 Brain Injury 43 0.032
271
PHH001 Phaeohyphomycosis 43 0.032
272
P MLG086 Malignant Hyperthermia Susceptibility 43 0.032
273
RFT001 Rift Valley Fever 43 0.032
274
RST001 Restless Legs Syndrome 42 0.032
275
PRT082 Preterm Premature Rupture of the Membranes 42 0.032
276
OCL001 Ocular Albinism 42 0.032
277
WLC001 Wolcott-Rallison Syndrome 42 0.032
278
P SCK005 Sickle Cell Disease 42 0.032
279
SYR002 Syringocystadenoma Papilliferum 42 0.032
280
ADL002 Adult Syndrome 42 0.032
281
PRP007 Priapism 42 0.032
282
ALB002 Albinism 42 0.032
283
CDQ001 Cauda Equina Syndrome 42 0.032
284
MMB002 Membranous Glomerulonephritis 41 0.032
285
P AML002 Amelogenesis Imperfecta 41 0.032
286
SCL003 Social Phobia 41 0.032
287
FSC004 Fasciitis 41 0.032
288
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 41 0.032
289
RCK002 Rocky Mountain Spotted Fever 41 0.032
290
TBR011 Tuberculous Meningitis 41 0.032
291
CYS005 Cysticercosis 40 0.032
292
P CRN074 Coronary Artery Aneurysm 40 0.032
293
JVN033 Juvenile Nasopharyngeal Angiofibroma 40 0.032
294
MSS002 Mass Syndrome 40 0.032
295
TBR008 Tuberculous Peritonitis 40 0.032
296
QDR001 Quadriplegia 40 0.032
297
PTT037 Pituitary Tumors 40 0.032
298
ANH002 Anhidrosis 40 0.032
299
P CHL066 Cholangitis 40 0.032
300
CWP001 Cowpox 40 0.032
301
c NTR038 Neutropenia, Severe Congenital 3, Autosomal Recessive 40 0.032
302
FCT001 Factor Viii Deficiency 40 0.032
303
SLP005 Sleep Disorder 40 0.032
304
PMP004 Pemphigus Foliaceus 40 0.032
305
PYL006 Pyloric Stenosis 39 0.032
306
P VTL001 Vitelliform Macular Dystrophy 39 0.032
307
CHN002 Chancroid 39 0.032
308
PRV006 Pervasive Developmental Disorder 39 0.032
309
SBC012 Subcorneal Pustular Dermatosis 39 0.032
310
CHR008 Choroiditis 39 0.032
311
SPN041 Spinal Cord Disease 39 0.032
312
INT017 Intestinal Schistosomiasis 39 0.032
313
PLY020 Polyradiculoneuropathy 39 0.032
314
PRL017 Prolymphocytic Leukemia 39 0.032
315
RSD004 Rosai-Dorfman Disease 39 0.032
316
DDN006 Duodenitis 39 0.032
317
P CTN015 Cutaneous T Cell Lymphoma 38 0.032
318
HYP025 Hyperphosphatemia 38 0.032
319
P PLN008 Peeling Skin Syndrome 38 0.032
320
CHR177 Chromophobe Renal Cell Carcinoma 38 0.032
321
NM001 Noma 38 0.032
322
NRS003 Neurosyphilis 38 0.032
323
c ACT042 Acute Pyelonephritis 38 0.032
324
RTR010 Retroperitoneal Sarcoma 38 0.032
325
PNN001 Panniculitis 38 0.032
326
BRN106 Burns 38 0.032
327
GRN039 Greenberg Skeletal Dysplasia 38 0.032
328
YWS001 Yaws 38 0.032
329
VLV020 Vulvar Melanoma 38 0.032
330
VSM001 Vasomotor Rhinitis 38 0.032
331
CVR006 Cavernous Hemangioma 38 0.032
332
SMN008 Semantic Dementia 37 0.032
333
CHR078 Chorioretinitis 37 0.032
334
LKM001 Leukemoid Reaction 37 0.032
335
IMP004 Impetigo 37 0.032
336
HDN002 Head Injury 37 0.032
337
LSS003 Lassa Fever 37 0.032
338
NVS001 Neovascular Glaucoma 37 0.032
339
GRN005 Granuloma Inguinale 37 0.032
340
SDD008 Sudden Sensorineural Hearing Loss 37 0.032
341
c HYP058 Hypervitaminosis a 37 0.032
342
TRC003 Trichomoniasis 36 0.032
343
URT008 Urticaria Pigmentosa 36 0.032
344
CRT015 Carotid Artery Occlusion 36 0.032
345
KWS001 Kwashiorkor 36 0.032
346
CRN025 Corneal Dystrophy 36 0.032
347
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 36 0.032
348
NRN002 Neuronitis 36 0.032
349
DDN011 Duodenal Atresia 35 0.032
350
FSR001 Fusariosis 35 0.032
351
ESP018 Esophageal Candidiasis 35 0.032
352
MYT011 Myotonia 35 0.032
353
c ACQ014 Acquired Hemophilia 35 0.032
354
LKC003 Leukocyte Disease 35 0.032
355
BLD053 Blood Platelet Disease 35 0.032
356
TRC077 Trichomegaly 35 0.032
357
DLY005 Delayed Sleep Phase Syndrome 35 0.032
358
GRM004 Germinoma 35 0.032
359
ANX004 Anoxia 34 0.032
360
PRP009 Peripartum Cardiomyopathy 34 0.032
361
c PRM023 Pre-Malignant Neoplasm 34 0.032
362
MYS004 Myiasis 34 0.032
363
DVL002 Developmental Disabilities 34 0.032
364
ERY017 Erythema Elevatum Diutinum 33 0.032
365
c ACQ042 Acquired Hemophilia a 33 0.032
366
RFL001 Reflex Sympathetic Dystrophy 33 0.032
367
GNG002 Ganglioneuroma 33 0.032
368
BST007 Best Vitelliform Macular Dystrophy 33 0.032
369
LNG004 Langerhans Cell Sarcoma 33 0.032
370
P SRT002 Sertoli Cell Tumor 33 0.032
371
LYM005 Lymphocele 32 0.032
372
HMN016 Hemangioendothelioma 32 0.032
373
P HRN001 Horner's Syndrome 32 0.032
374
VRT001 Vertebral Artery Occlusion 32 0.032
375
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 32 0.032
376
PRS025 Presbyopia 32 0.032
377
NCR007 Necrotizing Fasciitis 32 0.032
378
RFR003 Refractive Error 32 0.032
379
CHL052 Choledochal Cyst 32 0.032
380
c OST126 Osteopetrosis, Autosomal Recessive 1 32 0.032
381
P MRC003 Mercury Poisoning 31 0.032
382
PDT021 Pediatric Osteosarcoma 31 0.032
383
HYP048 Hypotropia 31 0.032
384
SYD001 Sydenham's Chorea 31 0.032
385
IMM127 Immune System Cancer 31 0.032
386
BRS004 Breast Angiosarcoma 31 0.032
387
c ACT004 Acute Diarrhea 31 0.032
388
TND005 Tendinitis 30 0.032
389
OBS004 Obstructive Hydrocephalus 30 0.032
390
c OST129 Osteopetrosis, Autosomal Recessive 2 30 0.032
391
PNM003 Pneumatosis Cystoides Intestinalis 30 0.032
392
CND006 Candida Glabrata 30 0.032
393
DYS073 Dysphagia 30 0.032
394
CMP035 Complete Atrioventricular Canal 30 0.032
395
BCL011 Bacillary Angiomatosis 29 0.032
396
c NTR039 Neutropenia, Severe Congenital 4, Autosomal Recessive 29 0.032
397
CRV030 Cervical Adenitis 29 0.032
398
c PLN018 Peeling Skin Syndrome 2 29 0.032
399
ENT005 Entropion 29 0.032
400
ART010 Arteriolosclerosis 28 0.032
401
NNS011 Nonseminomatous Germ Cell Tumor 28 0.032
402
PRX008 Paroxysmal Cold Hemoglobinuria 28 0.032
403
URT014 Ureterolithiasis 28 0.032
404
c ACT036 Acute Cholangitis 27 0.032
405
ANG037 Angiomatosis 27 0.032
406
HMX002 Heme Oxygenase-1 Deficiency 27 0.032
407
OPH001 Ophthalmomyiasis 26 0.032
408
P KRT059 Keratosis Palmoplantaris Striata 26 0.032
409
VBR003 Vibrio Vulnificus Infection 25 0.032
410
TNG004 Tongue Disease 24 0.032
411
END034 Endocrine Exophthalmos 24 0.032
412
TCK002 Tick Paralysis 24 0.032
413
NTR036 Neutropenia, Severe Congenital, X-Linked 24 0.032
414
P ACR072 Acrorenal Syndrome 23 0.032
415
c PLN017 Peeling Skin Syndrome 1 23 0.032
416
OCL003 Oculomotor Nerve Paralysis 23 0.032
417
LRY027 Laryngeal Papillomatosis 23 0.032
418
ERS002 Erosive Pustular Dermatosis of the Scalp 22 0.032
419
DYS135 Dysphagia Lusoria 21 0.032
420
c NTR037 Neutropenia, Severe Congenital 2, Autosomal Dominant 20 0.032
421
c NTR034 Neutropenia, Severe Congenital, 6, Autosomal Recessive 20 0.032
422
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 20 0.032
423
BNM011 Bone Marrow Failure Syndrome 2 20 0.032
424
c PRX067 Paroxysmal Nocturnal Hemoglobinuria 2 17 0.032
425
WHT007 White Platelet Syndrome 10 0.032
426
CHK002 Cheek Mucosa Cancer 10 0.032
427
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 8 0.032