MCID: THR014
MIFTS: 67

Thrombocytopenia

Categories: Blood diseases, Bone diseases, Genetic diseases, Immune diseases, Rare diseases

Aliases & Classifications for Thrombocytopenia

Summaries for Thrombocytopenia

KEGG : 37
Thrombocytopenia is defined by a decrease in the number of platelets in circulating blood, resulting in the potential for increased bleeding and decreased ability for clotting. Inherited syndromes are relatively rare causes of thrombocytopenia, but some genes underlying these disorders have been elucidated. Some inherited syndromes predispose to the development of bone marrow failure or leukemia. For example, familial platelet disorder with associated myeloid malignancy (FPDMM) is characterized by qualitative and quantitative platelet defects, and propensity to develop acute myelogenous leukemia.

MalaCards based summary : Thrombocytopenia is related to thrombocytopenia 1 and thrombocytopenia 2. An important gene associated with Thrombocytopenia is ETV6 (ETS Variant Transcription Factor 6), and among its related pathways/superpathways are Tight junction and Response to elevated platelet cytosolic Ca2+. The drugs Bivalirudin and Oprelvekin have been mentioned in the context of this disorder. Affiliated tissues include liver, bone and lung, and related phenotypes are cellular and hematopoietic system

Disease Ontology : 12 A blood platelet disease characterized by low a platelet count in the blood.

PubMed Health : 63 About thrombocytopenia: Thrombocytopenia (THROM-bo-si-to-PE-ne-ah) is a condition in which your blood has a lower than normal number of blood cell fragments called platelets (PLATE-lets). Platelets are made in your bone marrow along with other kinds of blood cells. They travel through your blood vessels and stick together (clot) to stop any bleeding that may happen if a blood vessel is damaged. Platelets also are called thrombocytes (THROM-bo-sites) because a clot also is called a thrombus.

Wikipedia : 75 Thrombocytopenia is a condition characterized by abnormally low levels of thrombocytes, also known as... more...

Related Diseases for Thrombocytopenia

Diseases in the Thrombocytopenia family:

Thrombocytopenia 2 Thrombocytopenia 3
Thrombocytopenia 1 Thrombocytopenia 4
Thrombocytopenia 5 Thrombocytopenia 6
Acquired Thrombocytopenia Thrombocytopenia Due to Platelet Alloimmunization
Primary Thrombocytopenia

Diseases related to Thrombocytopenia via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 1486, show less)
# Related Disease Score Top Affiliating Genes
1 thrombocytopenia 1 35.1 WAS HOXA11 GATA1
2 thrombocytopenia 2 34.7 MASTL ANKRD26
3 thrombocytopenia-absent radius syndrome 34.6 RBM8A MPL GP1BA GATA1 ANKRD26
4 autosomal thrombocytopenia with normal platelets 34.3 MASTL CYCS
5 myh-9 related disease 34.0 MYH9 GP1BA ANKRD26
6 platelet disorder, familial, with associated myeloid malignancy 33.4 ETV6 ANKRD26
7 thrombocytopenia due to platelet alloimmunization 33.3 MYH9 MPL ITGB3 ITGA2B ITGA2 GP9
8 thrombocytopenic purpura, autoimmune 33.2 MPL ITGB3 ITGA2B IL11 GP1BA
9 fetal and neonatal alloimmune thrombocytopenia 33.2 ITGB3 ITGA2B ITGA2 GP1BB GP1BA
10 primary thrombocytopenia 32.6 MYH9 MPL ITGB3 ITGA2B ITGA2 GP1BA
11 gray platelet syndrome 32.6 MASTL GP9 GATA1
12 pseudo-von willebrand disease 31.5 GP9 GP1BB GP1BA
13 bleeding disorder, platelet-type, 16 31.1 ITGB3 ITGA2B
14 bernard-soulier syndrome 31.1 MYH9 ITGB3 ITGA2B ITGA2 GP9 GP1BB
15 aplastic anemia 30.8 MPL ITGA2B IL11 GATA1
16 purpura 30.6 MPL ITGB3 ITGA2B GP1BB ADAMTS13
17 autosomal dominant macrothrombocytopenia 30.3 MYH9 ITGB3 ITGA2B GP1BB GP1BA
18 essential thrombocythemia 30.0 MPL ITGB3 ITGA2B IL11 GP1BA GATA1
19 aspirin resistance 29.9 ITGB3 ITGA2
20 hematologic cancer 29.9 MPL IL11 ETV6 CYCS
21 megakaryocytic leukemia 29.8 ITGA2B IL11 GATA1
22 hemorrhagic disease 29.7 MPL ITGA2B GP1BA ADAMTS13
23 thrombasthenia 29.6 ITGB3 ITGA2B ITGA2 GP9 GP1BA
24 hemorrhagic cystitis 29.6 IL11 CYCS
25 blood platelet disease 29.6 WAS MYH9 MPL ITGB3 ITGA2B GP9
26 glanzmann thrombasthenia 29.4 ITGB3 ITGA2B ITGA2 GP9 GP1BA
27 myocardial infarction 29.3 ITGB3 ITGA2B ITGA2 GP1BA ADAMTS13
28 von willebrand disease, type 2 29.0 ITGB3 ITGA2B ITGA2 GP1BA ADAMTS13
29 velocardiofacial syndrome 28.7 GP9 GP1BB GP1BA
30 amegakaryocytic thrombocytopenia, congenital 12.7
31 heparin-induced thrombocytopenia 12.7
32 thrombocytopenia with beta-thalassemia, x-linked 12.7
33 thrombocytopenia, paris-trousseau type 12.6
34 dyserythropoietic anemia and thrombocytopenia 12.6
35 thrombocytopenia, x-linked, with or without dyserythropoietic anemia 12.6
36 thrombocytopenia 5 12.6
37 thrombocytopenia 3 12.6
38 radioulnar synostosis with amegakaryocytic thrombocytopenia 1 12.6
39 thrombocytopenia 4 12.6
40 hemangioma-thrombocytopenia syndrome 12.5
41 thrombocytopenia 6 12.5
42 radioulnar synostosis with amegakaryocytic thrombocytopenia 2 12.5
43 radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome 12.5
44 acquired amegakaryocytic thrombocytopenia 12.5
45 thrombocytopenia, anemia, and myelofibrosis 12.5
46 acquired thrombocytopenia 12.4
47 myh9 related thrombocytopenia 12.4
48 transient neonatal thrombocytopenia 12.4
49 multifocal lymphangioendotheliomatosis with thrombocytopenia 12.3
50 thrombocytopenia, cyclic 12.3
51 hereditary thrombocytopenia with normal platelets 12.3
52 thrombocytopenia robin sequence 12.2
53 ankrd26-related thrombocytopenia 12.2
54 thrombocytopenia with elevated serum iga and renal disease 12.2
55 wiskott-aldrich syndrome 12.2
56 osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension 12.2
57 rare hemorrhagic disorder due to a constitutional thrombocytopenia 12.1
58 isolated constitutional thrombocytopenia 12.1
59 autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome 12.0
60 syndromic constitutional thrombocytopenia 12.0
61 obsolete: hereditary thrombocytopenia-hematological cancer predisposition syndrome 12.0
62 macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss 12.0
63 ivic syndrome 12.0
64 bleeding disorder, platelet-type, 17 12.0
65 thrombotic thrombocytopenic purpura 11.9
66 bleeding disorder, platelet-type, 20 11.9
67 dk phocomelia syndrome 11.9
68 evans' syndrome 11.9
69 deafness, autosomal dominant 1 11.8
70 hemolytic-uremic syndrome 11.8
71 hemolytic uremic syndrome, atypical 1 11.7
72 anemia, x-linked, with or without neutropenia and/or platelet abnormalities 11.6
73 autoimmune lymphoproliferative syndrome 11.6
74 jacobsen syndrome 11.5
75 thrombotic thrombocytopenic purpura, congenital 11.5
76 tau syndrome 11.5
77 sea-blue histiocyte disease 11.5
78 immunodysregulation, polyendocrinopathy, and enteropathy, x-linked 11.5
79 pearson marrow-pancreas syndrome 11.5
80 leukemia, acute lymphoblastic 11.4
81 digeorge syndrome 11.4
82 shwachman-diamond syndrome 1 11.4
83 bleeding disorder, platelet-type, 21 11.4
84 antiphospholipid syndrome 11.4
85 tafro syndrome 11.4
86 thrombocytosis 11.4
87 forsythe-wakeling syndrome 11.4
88 faye-petersen-ward-carey syndrome 11.4
89 dengue disease 11.3
90 bleeding disorder, platelet-type, 19 11.3
91 thrombotic microangiopathy 11.3
92 acute leukemia 11.3
93 dengue hemorrhagic fever 11.3
94 dengue virus 11.3
95 myeloma, multiple 11.3
96 severe pre-eclampsia 11.3
97 macrothrombocytopenia, autosomal dominant, tubb1-related 11.3
98 gaucher's disease 11.3
99 common variable immunodeficiency 11.3
100 viral hemorrhagic fever 11.3
101 stormorken syndrome 11.3
102 fanconi anemia, complementation group a 11.3
103 rare hemorrhagic disorder due to a platelet anomaly 11.3
104 rare hemorrhagic disorder due to an acquired platelet anomaly 11.3
105 rare hemorrhagic disorder due to a constitutional platelet anomaly 11.3
106 langerhans cell histiocytosis 11.3
107 acute promyelocytic leukemia 11.3
108 platelet glycoprotein iv deficiency 11.3
109 proteasome-associated autoinflammatory syndrome 1 11.3
110 dyskeratosis congenita 11.3
111 littoral cell angioma of the spleen 11.3
112 angioma, tufted 11.3
113 takenouchi-kosaki syndrome 11.3
114 niemann-pick disease 11.3
115 niemann-pick disease, type b 11.3
116 bleeding disorder, platelet-type, 9 11.3
117 bone marrow failure syndrome 4 11.3
118 large granular lymphocyte leukemia 11.3
119 thrombotic thrombocytopenic purpura, acquired 11.3
120 antiphospholipid syndrome, familial 11.1
121 bernard-soulier syndrome, type a2, autosomal dominant 11.1
122 aicardi-goutieres syndrome 1 11.1
123 osteopetrosis, autosomal recessive 5 11.1
124 tn polyagglutination syndrome 11.1
125 propionic acidemia 11.1
126 cerebroretinal microangiopathy with calcifications and cysts 1 11.1
127 nephrotic syndrome, type 7 11.1
128 pseudo-torch syndrome 2 11.1
129 proteasome-associated autoinflammatory syndrome 3 11.1
130 ataxia-pancytopenia syndrome 10.9
131 storage pool platelet disease 10.9
132 folate malabsorption, hereditary 10.9
133 gaucher disease, type iii 10.9
134 pseudo-torch syndrome 1 10.9
135 dihydropyrimidine dehydrogenase deficiency 10.9
136 autoimmune lymphoproliferative syndrome, type iia 10.9
137 transaldolase deficiency 10.9
138 spondyloenchondrodysplasia with immune dysregulation 10.9
139 gaucher disease, perinatal lethal 10.9
140 congenital disorder of glycosylation, type ih 10.9
141 aicardi-goutieres syndrome 2 10.9
142 aicardi-goutieres syndrome 3 10.9
143 aicardi-goutieres syndrome 4 10.9
144 thiopurines, poor metabolism of, 1 10.9
145 immunodeficiency 10 10.9
146 hemolytic uremic syndrome, atypical 2 10.9
147 hemolytic uremic syndrome, atypical 3 10.9
148 hemolytic uremic syndrome, atypical 4 10.9
149 hemolytic uremic syndrome, atypical 5 10.9
150 hemolytic uremic syndrome, atypical 6 10.9
151 aicardi-goutieres syndrome 5 10.9
152 lymphoproliferative syndrome 1 10.9
153 wiskott-aldrich syndrome 2 10.9
154 leukoencephalopathy, brain calcifications, and cysts 10.9
155 aicardi-goutieres syndrome 6 10.9
156 aicardi-goutieres syndrome 7 10.9
157 autoimmune lymphoproliferative syndrome, type v 10.9
158 epilepsy, hearing loss, and mental retardation syndrome 10.9
159 immunodeficiency 46 10.9
160 platelet abnormalities with eosinophilia and immune-mediated inflammatory disease 10.9
161 shwachman-diamond syndrome 2 10.9
162 argentine hemorrhagic fever 10.9
163 alkhurma hemorrhagic fever 10.9
164 aicardi-goutieres syndrome 10.9
165 congenital toxoplasmosis 10.9
166 acute myeloblastic leukemia with maturation 10.9
167 acute myeloblastic leukemia without maturation 10.9
168 acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) 10.9
169 autoimmune lymphoproliferative syndrome due to ctla4 haploinsuffiency 10.9
170 drug reaction with eosinophilia and systemic symptoms 10.9
171 fibular hemimelia 10.9
172 hemolytic uremic syndrome, atypical, childhood 10.9
173 core binding factor acute myeloid leukemia 10.9
174 cytogenetically normal acute myeloid leukemia 10.9
175 familial acute myeloid leukemia with mutated cebpa 10.9
176 neutropenia 10.8
177 thrombosis 10.8
178 deficiency anemia 10.7
179 autoimmune disease 10.7
180 hemolytic anemia 10.7
181 thrombophilia due to thrombin defect 10.7
182 lupus erythematosus 10.6
183 systemic lupus erythematosus 10.6
184 pulmonary embolism 10.6
185 disseminated intravascular coagulation 10.6
186 splenomegaly 10.6
187 acute basophilic leukemia 10.6 GATA1 ETV6
188 myelodysplastic syndrome 10.6
189 liver cirrhosis 10.6
190 liver disease 10.5
191 hepatitis c 10.5
192 pre-eclampsia 10.5
193 hypersplenism 10.5
194 myeloproliferative syndrome, transient 10.5 ITGB3 GP1BA GATA1
195 pulmonary fibrosis and/or bone marrow failure, telomere-related, 2 10.5
196 immune deficiency disease 10.5
197 kidney disease 10.5
198 acute kidney failure 10.5
199 lymphocytic leukemia 10.5
200 ischemia 10.5
201 malaria 10.4
202 hemangioma 10.4
203 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 10.4
204 exanthem 10.4
205 portal hypertension 10.4
206 pancytopenia 10.4
207 anemia, autoimmune hemolytic 10.4
208 hepatitis c virus 10.4
209 hematopoietic stem cell transplantation 10.4
210 granulocytopenia 10.4
211 von willebrand's disease 10.4
212 leukemia, chronic lymphocytic 10.4
213 leukemia, acute myeloid 10.4
214 leukemia, b-cell, chronic 10.4
215 myeloid leukemia 10.3
216 myelofibrosis 10.3
217 sarcoidosis 1 10.3
218 dermatitis 10.3
219 leukemia 10.3
220 eclampsia 10.3
221 pfeiffer syndrome 10.3
222 hepatitis 10.3
223 hemophilia 10.3
224 toxic shock syndrome 10.3
225 hellp syndrome 10.3
226 enterocolitis 10.3
227 respiratory failure 10.3
228 chickenpox 10.3
229 splenic sequestration 10.3
230 diarrhea 10.3
231 acquired immunodeficiency syndrome 10.3
232 cytomegalovirus infection 10.3
233 endocarditis 10.3
234 iron metabolism disease 10.2
235 end stage renal failure 10.2
236 graft-versus-host disease 10.2
237 perinatal necrotizing enterocolitis 10.2
238 glomerulonephritis 10.2
239 polycythemia 10.2
240 vasculitis 10.2
241 plasmodium vivax malaria 10.2
242 lymphopenia 10.2
243 rubella 10.2
244 intermediate coronary syndrome 10.2
245 acute myocardial infarction 10.2
246 allergic hypersensitivity disease 10.2
247 severe combined immunodeficiency 10.2
248 bone marrow cancer 10.2 MPL ITGB3 IL11 GATA1 ETV6
249 human immunodeficiency virus type 1 10.2
250 pulmonary hypertension 10.2
251 connective tissue disease 10.2
252 cytokine deficiency 10.2
253 hepatocellular carcinoma 10.2
254 limb ischemia 10.2
255 lymphoproliferative syndrome 10.2
256 iron deficiency anemia 10.2
257 thrombophilia 10.2
258 hyperthyroidism 10.2
259 portal vein thrombosis 10.2
260 macrothrombocytopenia with mitral valve insufficiency 10.2
261 colorectal cancer 10.2
262 lymphoma 10.2
263 brucellosis 10.2
264 hypereosinophilic syndrome 10.2
265 leptospirosis 10.2
266 pneumonia 10.2
267 congestive heart failure 10.2
268 cardiogenic shock 10.2
269 hemophagocytic lymphohistiocytosis 10.1
270 cardiac arrest 10.1
271 vascular disease 10.1
272 pulmonary tuberculosis 10.1
273 histiocytosis 10.1
274 47,xyy 10.1
275 factor viii deficiency 10.1
276 hemophilia a 10.1
277 budd-chiari syndrome 10.1
278 autosomal recessive disease 10.1
279 bacterial infectious disease 10.1
280 hypothyroidism 10.1
281 hemoglobinuria 10.1
282 helicobacter pylori infection 10.1
283 colitis 10.1
284 hepatitis b 10.1
285 ulcerative colitis 10.1
286 red cell aplasia 10.1
287 varicose veins 10.1
288 thalassemia 10.1
289 heart disease 10.1
290 plasmodium falciparum malaria 10.1
291 giant hemangioma 10.1
292 b-cell lymphoma 10.1
293 thyroiditis 10.1
294 encephalopathy 10.1
295 polycythemia vera 10.1
296 branchiootic syndrome 1 10.1
297 angiosarcoma 10.1
298 nephrotic syndrome 10.1
299 graves' disease 10.1
300 pure red-cell aplasia 10.1
301 aortic aneurysm 10.1
302 systemic scleroderma 10.1
303 cataract 10.1
304 48,xyyy 10.1
305 renal cell carcinoma, nonpapillary 10.1
306 graves disease 1 10.1
307 hydrocephalus 10.1
308 synostosis 10.1
309 viral hepatitis 10.1
310 cerebrovascular disease 10.1
311 measles 10.1
312 encephalitis 10.1
313 gata1-related x-linked cytopenia 10.1
314 congenital hydrocephalus 10.1
315 aneurysm 10.1
316 down syndrome 10.1
317 leukemia, chronic myeloid 10.1
318 kawasaki disease 10.1
319 paroxysmal nocturnal hemoglobinuria 10.1
320 lymphadenitis 10.1
321 heart septal defect 10.1
322 myeloproliferative neoplasm 10.1
323 glioblastoma multiforme 10.1
324 gastritis 10.1
325 glioblastoma 10.1
326 gaucher disease, type i 10.0
327 myasthenia gravis 10.0
328 stroke, ischemic 10.0
329 patent ductus arteriosus 1 10.0
330 inflammatory bowel disease 10.0
331 infective endocarditis 10.0
332 hepatitis a 10.0
333 pustulosis of palm and sole 10.0
334 pancreatitis 10.0
335 chronic kidney disease 10.0
336 myocarditis 10.0
337 arthritis 10.0
338 psoriasis 10.0
339 macroglobulinemia 10.0
340 acute respiratory distress syndrome 10.0
341 chromosomal triplication 10.0
342 phocomelia 10.0
343 headache 10.0
344 aortic aneurysm, familial abdominal, 1 10.0
345 ovarian cancer 10.0
346 rheumatoid arthritis 10.0
347 scleroderma, familial progressive 10.0
348 lung cancer 10.0
349 mycobacterium tuberculosis 1 10.0
350 epidemic typhus 10.0
351 vitamin b12 deficiency 10.0
352 mumps 10.0
353 autoimmune hepatitis 10.0
354 relapsing-remitting multiple sclerosis 10.0
355 thrombophlebitis 10.0
356 crohn's disease 10.0
357 acute graft versus host disease 10.0
358 myositis 10.0
359 platelet aggregation, spontaneous 10.0
360 congenital heart defects, hamartomas of tongue, and polysyndactyly 10.0
361 multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 10.0
362 thymoma, familial 10.0
363 peripheral vascular disease 10.0
364 dengue shock syndrome 10.0
365 korean hemorrhagic fever 10.0
366 pain agnosia 10.0
367 esophageal varix 10.0
368 hemorrhagic fever with renal syndrome 10.0
369 coronary thrombosis 10.0
370 cholestasis 10.0
371 mitral valve stenosis 10.0
372 thymoma 10.0
373 compartment syndrome 10.0
374 influenza 10.0
375 subacute delirium 10.0
376 neuropathy 10.0
377 hypoglycemia 10.0
378 chronic graft versus host disease 10.0
379 hemangioendothelioma 10.0
380 seizure disorder 10.0
381 acute liver failure 10.0
382 kaposi sarcoma 10.0
383 lymphoma, hodgkin, classic 10.0
384 yemenite deaf-blind hypopigmentation syndrome 10.0
385 hydrops, lactic acidosis, and sideroblastic anemia 10.0
386 ehrlichiosis 10.0
387 sarcoma 10.0
388 pulmonary edema 10.0
389 visual epilepsy 10.0
390 primary biliary cirrhosis 10.0
391 acute cystitis 10.0
392 typhoid fever 10.0
393 scrub typhus 10.0
394 megaloblastic anemia 10.0
395 polyneuropathy 10.0
396 atrial heart septal defect 10.0
397 mixed connective tissue disease 10.0
398 placental insufficiency 10.0
399 syphilis 10.0
400 myopathy 10.0
401 spindle cell sarcoma 10.0
402 uremia 10.0
403 peritonitis 10.0
404 fatty liver disease 10.0
405 was-related disorders 10.0
406 primary biliary cholangitis 10.0
407 angiomatosis 10.0
408 rare surgical neurologic disease 10.0
409 alcohol dependence 9.9
410 ocular motor apraxia 9.9
411 wilms tumor 5 9.9
412 aspergillosis 9.9
413 glucocorticoid resistance, generalized 9.9
414 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 9.9
415 hyperlipoproteinemia, type iii 9.9
416 tick-borne encephalitis 9.9
417 follicular lymphoma 9.9
418 immunoglobulin alpha deficiency 9.9
419 porencephaly 9.9
420 chronic myelomonocytic leukemia 9.9
421 angioimmunoblastic t-cell lymphoma 9.9
422 trypanosomiasis 9.9
423 spotted fever 9.9
424 tetanus 9.9
425 coronary artery anomaly 9.9
426 amenorrhea 9.9
427 transient cerebral ischemia 9.9
428 splenic infarction 9.9
429 agammaglobulinemia 9.9
430 bilirubin metabolic disorder 9.9
431 active peptic ulcer disease 9.9
432 lung disease 9.9
433 herpes simplex 9.9
434 placental abruption 9.9
435 alopecia 9.9
436 catastrophic antiphospholipid syndrome 9.9
437 rapidly involuting congenital hemangioma 9.9
438 refractory anemia 9.9
439 breast cancer 9.9
440 multiple sclerosis 9.9
441 fibrosis of extraocular muscles, congenital, 1 9.9
442 hashimoto thyroiditis 9.9
443 triiodothyronine receptor auxiliary protein 9.9
444 pancreatic cancer 9.9
445 gastric cancer 9.9
446 bacterial sepsis 9.9
447 autoimmune pancreatitis 9.9
448 human granulocytic anaplasmosis 9.9
449 diffuse large b-cell lymphoma 9.9
450 mantle cell lymphoma 9.9
451 atrioventricular block 9.9
452 castleman disease 9.9
453 malignant hypertension 9.9
454 amnestic disorder 9.9
455 pituitary apoplexy 9.9
456 cardiac tamponade 9.9
457 mitral valve insufficiency 9.9
458 poems syndrome 9.9
459 alcohol use disorder 9.9
460 rectum cancer 9.9
461 protein c deficiency 9.9
462 combined t cell and b cell immunodeficiency 9.9
463 viral infectious disease 9.9
464 meningitis 9.9
465 inherited bone marrow failure syndromes 9.9
466 posttransplant acute limbic encephalitis 9.9
467 arteries, anomalies of 9.9
468 exudative vitreoretinopathy 1 9.9
469 hypercholesterolemia, familial, 1 9.9
470 radioulnar synostosis 9.9
471 celiac disease 1 9.9
472 diabetes mellitus, ketosis-prone 9.9
473 cyanosis, transient neonatal 9.9
474 leukemia, acute lymphoblastic 3 9.9
475 rocky mountain spotted fever 9.9
476 atrial fibrillation 9.9
477 drug allergy 9.9
478 dermatomyositis 9.9
479 interstitial nephritis 9.9
480 gastric ulcer 9.9
481 alport syndrome 9.9
482 adult respiratory distress syndrome 9.9
483 diphtheria 9.9
484 hemopericardium 9.9
485 hemosiderosis 9.9
486 osteopetrosis 9.9
487 polyclonal hypergammaglobulinemia 9.9
488 hemangioma of spleen 9.9
489 hairy cell leukemia 9.9
490 acute pancreatitis 9.9
491 iga glomerulonephritis 9.9
492 adenocarcinoma 9.9
493 lipid metabolism disorder 9.9
494 teratoma 9.9
495 hepatitis e 9.9
496 peripheral nervous system disease 9.9
497 bullous pemphigoid 9.9
498 malignant histiocytosis 9.9
499 diabetes mellitus 9.9
500 miliary tuberculosis 9.9
501 microcephaly 9.9
502 chronic thromboembolic pulmonary hypertension 9.9
503 hypoxia 9.9
504 syncope 9.9
505 traumatic brain injury 9.9
506 congenital hemangioma 9.9
507 pik3ca-related overgrowth syndrome 9.9
508 refractory cytopenia with multilineage dysplasia 9.9
509 acute adrenal insufficiency 9.9
510 migraine with or without aura 1 9.8
511 noonan syndrome 1 9.8
512 pernicious anemia 9.8
513 prostate cancer 9.8
514 small cell cancer of the lung 9.8
515 felty syndrome 9.8
516 erythroleukemia, familial 9.8
517 cornelia de lange syndrome 1 9.8
518 hemophilia b 9.8
519 ventricular fibrillation, paroxysmal familial, 1 9.8
520 pulmonary disease, chronic obstructive 9.8
521 major affective disorder 8 9.8
522 major affective disorder 9 9.8
523 pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis 9.8
524 beta-thalassemia 9.8
525 aortic valve disease 2 9.8
526 angina pectoris 9.8
527 aphasia 9.8
528 ptosis 9.8
529 zika fever 9.8
530 non-alcoholic fatty liver disease 9.8
531 multicentric castleman disease 9.8
532 meningoencephalitis 9.8
533 hemiplegia 9.8
534 asphyxia neonatorum 9.8
535 pyelonephritis 9.8
536 cornelia de lange syndrome 9.8
537 lyme disease 9.8
538 pericardial effusion 9.8
539 conn's syndrome 9.8
540 acute kidney tubular necrosis 9.8
541 guillain-barre syndrome 9.8
542 acute proliferative glomerulonephritis 9.8
543 coccidioidomycosis 9.8
544 acute poststreptococcal glomerulonephritis 9.8
545 candidiasis 9.8
546 urticaria 9.8
547 pneumothorax 9.8
548 cystitis 9.8
549 pericarditis 9.8
550 cerebral palsy 9.8
551 gastroenteritis 9.8
552 hemoglobinopathy 9.8
553 cryoglobulinemia 9.8
554 anuria 9.8
555 rhabdomyosarcoma 9.8
556 bipolar disorder 9.8
557 cellulitis 9.8
558 sagittal sinus thrombosis 9.8
559 intracranial thrombosis 9.8
560 poliomyelitis 9.8
561 juvenile rheumatoid arthritis 9.8
562 peptic ulcer disease 9.8
563 collagen disease 9.8
564 hodgkin's lymphoma, lymphocytic-histiocytic predominance 9.8
565 bacterial meningitis 9.8
566 babesiosis 9.8
567 toxoplasmosis 9.8
568 adrenomyeloneuropathy 9.8
569 afibrinogenemia 9.8
570 cold agglutinin disease 9.8
571 congenital radioulnar synostosis 9.8
572 congenital rubella 9.8
573 germ cells tumors 9.8
574 pseudo-turner syndrome 9.8
575 zika virus infection 9.8
576 back pain 9.8
577 dysphagia 9.8
578 tremor 9.8
579 rare hereditary hemochromatosis 9.8
580 histiocytic sarcoma 9.8
581 rare disease in surgical orthopedic 9.8
582 polyploidy 9.8
583 intravascular large b-cell lymphoma 9.8
584 osteoporosis 9.8
585 pulmonary hypertension, primary, 1 9.8
586 retinal detachment 9.8
587 schistosoma mansoni infection, susceptibility/ 9.8
588 thrombophilia due to activated protein c resistance 9.8
589 vitiligo-associated multiple autoimmune disease susceptibility 6 9.8
590 hypertriglyceridemia, familial 9.8
591 hpa i recognition polymorphism, beta-globin-related 9.8
592 hair whorl 9.8
593 cryoglobulinemia, familial mixed 9.8
594 progressive familial heart block, type ia 9.8
595 bladder cancer 9.8
596 atrial standstill 1 9.8
597 spondyloarthropathy 1 9.8
598 cystic fibrosis 9.8
599 roberts syndrome 9.8
600 sjogren syndrome 9.8
601 adrenoleukodystrophy 9.8
602 ataxia and polyneuropathy, adult-onset 9.8
603 lymphoma, non-hodgkin, familial 9.8
604 vitiligo-associated multiple autoimmune disease susceptibility 1 9.8
605 anorexia nervosa 9.8
606 creatinine clearance quantitative trait locus 9.8
607 granulomatosis with polyangiitis 9.8
608 bone mineral density quantitative trait locus 8 9.8
609 lung cancer susceptibility 3 9.8
610 microvascular complications of diabetes 3 9.8
611 microvascular complications of diabetes 4 9.8
612 microvascular complications of diabetes 6 9.8
613 microvascular complications of diabetes 7 9.8
614 bone mineral density quantitative trait locus 15 9.8
615 alacrima, achalasia, and mental retardation syndrome 9.8
616 encephalopathy, progressive, early-onset, with episodic rhabdomyolysis 9.8
617 chikungunya 9.8
618 aspiration pneumonia 9.8
619 severe congenital neutropenia 9.8
620 chorioamnionitis 9.8
621 withdrawal disorder 9.8
622 lymphoblastic lymphoma 9.8
623 sleeping sickness 9.8
624 osteomyelitis 9.8
625 tonsillitis 9.8
626 qualitative platelet defect 9.8
627 microcytic anemia 9.8
628 gestational diabetes 9.8
629 cortical blindness 9.8
630 inflammatory spondylopathy 9.8
631 crimean-congo hemorrhagic fever 9.8
632 dilated cardiomyopathy 9.8
633 carotid stenosis 9.8
634 transient global amnesia 9.8
635 rift valley fever 9.8
636 schistosomiasis 9.8
637 adult-onset still's disease 9.8
638 mixed malaria 9.8
639 neuroleptic malignant syndrome 9.8
640 papilledema 9.8
641 lymphangioma 9.8
642 arthus reaction 9.8
643 rheumatic disease 9.8
644 ventricular septal defect 9.8
645 histoplasmosis 9.8
646 squamous cell carcinoma 9.8
647 melanoma 9.8
648 cholecystitis 9.8
649 leiomyosarcoma 9.8
650 macrocytic anemia 9.8
651 splenic abscess 9.8
652 chorioangioma 9.8
653 idiopathic interstitial pneumonia 9.8
654 chronic granulomatous disease 9.8
655 arthropathy 9.8
656 insulinoma 9.8
657 merkel cell carcinoma 9.8
658 coronary stenosis 9.8
659 milk allergy 9.8
660 hypokalemia 9.8
661 rapidly progressive glomerulonephritis 9.8
662 thyroid gland disease 9.8
663 ovarian cyst 9.8
664 urinary tract obstruction 9.8
665 hemangioblastoma 9.8
666 human immunodeficiency virus infectious disease 9.8
667 intestinal disease 9.8
668 paraplegia 9.8
669 adenoma 9.8
670 spondylitis 9.8
671 monoclonal gammopathy of uncertain significance 9.8
672 cocaine abuse 9.8
673 localized scleroderma 9.8
674 erythema infectiosum 9.8
675 amyloidosis 9.8
676 cholangitis 9.8
677 stomatitis 9.8
678 congenital syphilis 9.8
679 hypoplastic left heart syndrome 9.8
680 congenital hepatic fibrosis 9.8
681 sall4-related disorders 9.8
682 sickle cell disease 9.8
683 acquired hemophilia 9.8
684 acquired hemophilia a 9.8
685 banti's syndrome 9.8
686 congenital cytomegalovirus 9.8
687 coronary artery aneurysm 9.8
688 encephalocele 9.8
689 fetal edema 9.8
690 giant cell myocarditis 9.8
691 glioma 9.8
692 haemophilus influenzae 9.8
693 hydrops fetalis 9.8
694 lymphocytic hypophysitis 9.8
695 lymphosarcoma 9.8
696 meningococcemia 9.8
697 wandering spleen 9.8
698 raynaud phenomenon 9.8
699 depression 9.8
700 head injury 9.8
701 pituitary tumors 9.8
702 glial tumor 9.8
703 rare lymphatic malformation 9.8
704 diffuse alveolar hemorrhage 9.8
705 hepatosplenic t-cell lymphoma 9.8
706 pediatric systemic lupus erythematosus 9.8
707 platelet groups--ko system 9.7
708 anemia, hypochromic microcytic, with iron overload 1 9.7
709 sitosterolemia 9.7
710 tetralogy of fallot 9.7
711 strabismus 9.7
712 teratoma, ovarian 9.7
713 chromosome 5q deletion syndrome 9.7
714 lipomatosis, multiple 9.7
715 leukemia, acute monocytic 9.7
716 ige responsiveness, atopic 9.7
717 hypertension, essential 9.7
718 holt-oram syndrome 9.7
719 immunoglobulin a deficiency 1 9.7
720 cleft palate, isolated 9.7
721 cardiac arrhythmia 9.7
722 blue rubber bleb nevus 9.7
723 neurofibromatosis, type ii 9.7
724 eosinophilic fasciitis 9.7
725 factor v deficiency 9.7
726 hydrocephalus, congenital, 1 9.7
727 hypervitaminosis a 9.7
728 neuroblastoma 1 9.7
729 3-methylglutaconic aciduria, type iii 9.7
730 schizencephaly 9.7
731 mayer-rokitansky-kuster-hauser syndrome 9.7
732 wilson disease 9.7
733 neutropenia, severe congenital, x-linked 9.7
734 prostatic hyperplasia, benign 9.7
735 adenomyosis 9.7
736 aceruloplasminemia 9.7
737 progressive familial heart block, type ib 9.7
738 gastrointestinal stromal tumor 9.7
739 endometrial cancer 9.7
740 myocardial infarction 2 9.7
741 fatty liver disease, nonalcoholic 1 9.7
742 membranous nephropathy 9.7
743 melioidosis 9.7
744 cholangiocarcinoma 9.7
745 carbonic anhydrase va deficiency, hyperammonemia due to 9.7
746 chorea, childhood-onset, with psychomotor retardation 9.7
747 spastic paraplegia, intellectual disability, nystagmus, and obesity 9.7
748 mucopolysaccharidosis-plus syndrome 9.7
749 polymicrogyria with or without vascular-type ehlers-danlos syndrome 9.7
750 cryptogenic organizing pneumonia 9.7
751 hypophosphatemia 9.7
752 hyperphosphatemia 9.7
753 variola major 9.7
754 hypochromic microcytic anemia 9.7
755 marginal zone b-cell lymphoma 9.7
756 splenic marginal zone lymphoma 9.7
757 metabolic acidosis 9.7
758 marantic endocarditis 9.7
759 crohn's colitis 9.7
760 scoliosis 9.7
761 griscelli syndrome 9.7
762 bone disease 9.7
763 bone resorption disease 9.7
764 cryptococcal meningitis 9.7
765 mucositis 9.7
766 igg4-related disease 9.7
767 sensorineural hearing loss 9.7
768 cerebral artery occlusion 9.7
769 pleomorphic lipoma 9.7
770 cholelithiasis 9.7
771 pleurisy 9.7
772 common cold 9.7
773 nasopharyngitis 9.7
774 short bowel syndrome 9.7
775 open-angle glaucoma 9.7
776 japanese encephalitis 9.7
777 hydronephrosis 9.7
778 prostatic hypertrophy 9.7
779 pertussis 9.7
780 t cell deficiency 9.7
781 primary hyperparathyroidism 9.7
782 plethora of newborn 9.7
783 erysipelas 9.7
784 hepatorenal syndrome 9.7
785 clubfoot 9.7
786 vaginal cancer 9.7
787 chagas disease 9.7
788 goiter 9.7
789 hepatic coma 9.7
790 telangiectasis 9.7
791 choreatic disease 9.7
792 relapsing fever 9.7
793 focal segmental glomerulosclerosis 9.7
794 uveitis 9.7
795 gout 9.7
796 right bundle branch block 9.7
797 porphyria 9.7
798 mycoplasma pneumoniae pneumonia 9.7
799 hepatic encephalopathy 9.7
800 hyperparathyroidism 9.7
801 obstructive jaundice 9.7
802 biliary atresia 9.7
803 patent foramen ovale 9.7
804 familial hypercholesterolemia 9.7
805 facial paralysis 9.7
806 alcoholic liver cirrhosis 9.7
807 bipolar i disorder 9.7
808 capillary leak syndrome 9.7
809 duodenal ulcer 9.7
810 optic nerve disease 9.7
811 hyperinsulinism 9.7
812 enthesopathy 9.7
813 focal epilepsy 9.7
814 granulomatous hepatitis 9.7
815 colon adenocarcinoma 9.7
816 myelophthisic anemia 9.7
817 protein s deficiency 9.7
818 angiodysplasia 9.7
819 transitional cell carcinoma 9.7
820 acute interstitial pneumonia 9.7
821 prostatic adenoma 9.7
822 membranoproliferative glomerulonephritis 9.7
823 severe acute respiratory syndrome 9.7
824 germ cell cancer 9.7
825 testicular cancer 9.7
826 substance abuse 9.7
827 interstitial lung disease 9.7
828 myelitis 9.7
829 fibrosarcoma 9.7
830 carotid artery disease 9.7
831 breast adenocarcinoma 9.7
832 mastocytosis 9.7
833 lactic acidosis 9.7
834 intermittent claudication 9.7
835 plasmacytoma 9.7
836 pulmonary fibrosis 9.7
837 pituitary adenoma 9.7
838 intestinal pseudo-obstruction 9.7
839 acute myocarditis 9.7
840 bladder urothelial carcinoma 9.7
841 pancreatic adenocarcinoma 9.7
842 heart valve disease 9.7
843 intracranial embolism 9.7
844 clear cell renal cell carcinoma 9.7
845 rhinitis 9.7
846 subacute bacterial endocarditis 9.7
847 endophthalmitis 9.7
848 proliferative glomerulonephritis 9.7
849 immune-complex glomerulonephritis 9.7
850 cavernous hemangioma 9.7
851 intrahepatic cholangiocarcinoma 9.7
852 testicular germ cell cancer 9.7
853 ovarian germ cell teratoma 9.7
854 acute pyelonephritis 9.7
855 inferior myocardial infarction 9.7
856 conjunctivitis 9.7
857 t-cell leukemia 9.7
858 situs inversus 9.7
859 appendicitis 9.7
860 monocytic leukemia 9.7
861 herpes zoster 9.7
862 malignant hyperthermia 9.7
863 smallpox 9.7
864 mechanical strabismus 9.7
865 diabetes insipidus 9.7
866 bronchiectasis 9.7
867 fasciitis 9.7
868 aphthous stomatitis 9.7
869 alopecia areata 9.7
870 periostitis 9.7
871 drug dependence 9.7
872 hypertrophic cardiomyopathy 9.7
873 polymicrogyria 9.7
874 acquired pure red cell aplasia 9.7
875 acute monoblastic leukemia 9.7
876 anca-associated vasculitis 9.7
877 cytomegalic inclusion disease 9.7
878 dwarfism 9.7
879 fetal thalidomide syndrome 9.7
880 hemophagocytic reticulosis 9.7
881 hereditary antithrombin deficiency 9.7
882 homologous wasting disease 9.7
883 horseshoe kidney 9.7
884 hypoadrenalism 9.7
885 hypoaldosteronism 9.7
886 kaposiform hemangioendothelioma 9.7
887 leukemia, t-cell, chronic 9.7
888 may-thurner syndrome 9.7
889 neisseria meningitidis infection 9.7
890 non-involuting congenital hemangioma 9.7
891 retroperitoneal fibrosis 9.7
892 syndrome of inappropriate antidiuretic hormone 9.7
893 systemic capillary leak syndrome 9.7
894 brain injury 9.7
895 hypotonia 9.7
896 paraneoplastic syndromes 9.7
897 monosomy 21 9.7
898 systemic autoimmune disease 9.7
899 cerebrofacial arteriovenous metameric syndrome 9.7
900 hemolytic disease due to fetomaternal alloimmunization 9.7
901 neonatal alloimmune neutropenia 9.7
902 acute radiation syndrome 9.7
903 avascular necrosis 9.7
904 rare tumor 9.7
905 overgrowth syndrome 9.7
906 thyroid carcinoma 9.7
907 autoimmune disease of blood 9.5 MPL ITGB3 ITGA2B ITGA2 GP1BA ADAMTS13
908 tracheoesophageal fistula with or without esophageal atresia 9.5
909 suppressor of tumorigenicity 3 9.5
910 renal hypodysplasia/aplasia 1 9.5
911 vesicoureteral reflux 1 9.5
912 wolf-hirschhorn syndrome 9.5
913 abetalipoproteinemia 9.5
914 anus, imperforate 9.5
915 ataxia-telangiectasia 9.5
916 c syndrome 9.5
917 congenital disorder of glycosylation, type i/iix 9.5
918 premature centromere division 9.5
919 cerebrotendinous xanthomatosis 9.5
920 cholesterol pneumonia 9.5
921 telecanthus 9.5
922 odontochondrodysplasia 9.5
923 sneddon syndrome 9.5
924 dowling-degos disease 1 9.5
925 pulmonary hemosiderosis 9.5
926 proline-negative auxotroph of hamster, complementation of 9.5
927 pectus excavatum 9.5
928 papillomatosis, confluent and reticulated 9.5
929 nephrolithiasis, calcium oxalate 9.5
930 otitis media 9.5
931 neutrophilia, hereditary 9.5
932 cyclic neutropenia 9.5
933 neurofibromatosis, type iv, of riccardi 9.5
934 meckel diverticulum 9.5
935 inclusion body myositis 9.5
936 hypertelorism 9.5
937 attention deficit-hyperactivity disorder 9.5
938 hernia, hiatus 9.5
939 diaphragmatic hernia, congenital 9.5
940 heinz body anemias 9.5
941 glaucoma, primary open angle 9.5
942 lymphoma, mucosa-associated lymphoid type 9.5
943 esophageal cancer 9.5
944 erythrokeratodermia variabilis et progressiva 1 9.5
945 preauricular fistulae, congenital 9.5
946 cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 9.5
947 split-hand/foot malformation with long bone deficiency 1 9.5
948 cerebral cavernous malformations 9.5
949 burkitt lymphoma 9.5
950 aortic valve disease 1 9.5
951 gastroesophageal reflux 9.5
952 arteriovenous malformations of the brain 9.5
953 aniridia 1 9.5
954 amyotrophic lateral sclerosis 1 9.5
955 achondroplasia 9.5
956 chondrosarcoma 9.5
957 chordoma 9.5
958 cohen syndrome 9.5
959 complement component 2 deficiency 9.5
960 baller-gerold syndrome 9.5
961 diastrophic dysplasia 9.5
962 duodenal atresia 9.5
963 factor vii deficiency 9.5
964 fanconi anemia, complementation group c 9.5
965 galactorrhea 9.5
966 factor xii deficiency 9.5
967 heart block, congenital 9.5
968 hemochromatosis, type 1 9.5
969 mckusick-kaufman syndrome 9.5
970 hyperlipoproteinemia, type i 9.5
971 ichthyosis, congenital, autosomal recessive 4b 9.5
972 schimke immunoosseous dysplasia 9.5
973 intracranial hypertension, idiopathic 9.5
974 keutel syndrome 9.5
975 microcephaly 1, primary, autosomal recessive 9.5
976 moyamoya disease 1 9.5
977 mucolipidosis ii alpha/beta 9.5
978 mucopolysaccharidosis, type vi 9.5
979 galactosialidosis 9.5
980 nonarteritic anterior ischemic optic neuropathy 9.5
981 osteogenic sarcoma 9.5
982 osteopetrosis, autosomal recessive 1 9.5
983 panencephalitis, subacute sclerosing 9.5
984 pituitary hormone deficiency, combined, 2 9.5
985 porphyria, congenital erythropoietic 9.5
986 respiratory distress syndrome in premature infants 9.5
987 rhabdomyosarcoma 2 9.5
988 rheumatic fever-related antigen 9.5
989 sc phocomelia syndrome 9.5
990 smith-lemli-opitz syndrome 9.5
991 testicular germ cell tumor 9.5
992 tibial hemimelia 9.5
993 opitz gbbb syndrome, type i 9.5
994 intestinal pseudoobstruction, neuronal, chronic idiopathic, x-linked 9.5
995 androgen insensitivity syndrome 9.5
996 body mass index quantitative trait locus 11 9.5
997 radial ray deficiency, x-linked 9.5
998 sarcoma, synovial 9.5
999 dyskeratosis congenita, x-linked 9.5
1000 isolated growth hormone deficiency, type iii, with agammaglobulinemia 9.5
1001 mucopolysaccharidosis, type ii 9.5
1002 thoracoabdominal syndrome 9.5
1003 kearns-sayre syndrome 9.5
1004 pituitary adenoma, prolactin-secreting 9.5
1005 mullerian duct aplasia, unilateral renal agenesis, and cervicothoracic somite anomalies 9.5
1006 spastic paraplegia and evans syndrome 9.5
1007 quebec platelet disorder 9.5
1008 body mass index quantitative trait locus 9 9.5
1009 xanthomatosis 9.5
1010 macular degeneration, age-related, 1 9.5
1011 dermatitis, atopic 9.5
1012 homocysteinemia 9.5
1013 body mass index quantitative trait locus 8 9.5
1014 cerebral cavernous malformations 3 9.5
1015 hemophagocytic lymphohistiocytosis, familial, 2 9.5
1016 sickle cell anemia 9.5
1017 microvascular complications of diabetes 1 9.5
1018 cervical cancer 9.5
1019 reflex sympathetic dystrophy 9.5
1020 orthostatic intolerance 9.5
1021 hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy 9.5
1022 nonaka myopathy 9.5
1023 atrioventricular septal defect 9.5
1024 body mass index quantitative trait locus 1 9.5
1025 aortic aneurysm, familial thoracic 1 9.5
1026 nasopharyngeal carcinoma 9.5
1027 allergic rhinitis 9.5
1028 body mass index quantitative trait locus 4 9.5
1029 body mass index quantitative trait locus 10 9.5
1030 juvenile myelomonocytic leukemia 9.5
1031 anxiety 9.5
1032 neutrophilic dermatosis, acute febrile 9.5
1033 kala-azar 1 9.5
1034 body mass index quantitative trait locus 7 9.5
1035 legionnaire disease 9.5
1036 hypertension, diastolic 9.5
1037 choanal atresia, posterior 9.5
1038 mevalonic aciduria 9.5
1039 retinal cone dystrophy 4 9.5
1040 systemic lupus erythematosus 9 9.5
1041 congenital disorder of glycosylation, type in 9.5
1042 ewing sarcoma 9.5
1043 body mass index quantitative trait locus 12 9.5
1044 body mass index quantitative trait locus 14 9.5
1045 microvascular complications of diabetes 2 9.5
1046 microvascular complications of diabetes 5 9.5
1047 premature ovarian failure 7 9.5
1048 antithrombin iii deficiency 9.5
1049 tumor predisposition syndrome 9.5
1050 complement component 4a deficiency 9.5
1051 peripartum cardiomyopathy 9.5
1052 body mass index quantitative trait locus 18 9.5
1053 hyperprolactinemia 9.5
1054 analbuminemia 9.5
1055 corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia 9.5
1056 retinitis pigmentosa and erythrocytic microcytosis 9.5
1057 erythrokeratodermia variabilis et progressiva 4 9.5
1058 helix syndrome 9.5
1059 alkuraya-kucinskas syndrome 9.5
1060 body mass index quantitative trait locus 19 9.5
1061 body mass index quantitative trait locus 20 9.5
1062 west syndrome 9.5
1063 aspirin allergy 9.5
1064 streptococcus pneumonia 9.5
1065 drug-induced lupus erythematosus 9.5
1066 autoimmune vasculitis 9.5
1067 pemphigus gestationis 9.5
1068 human monocytic ehrlichiosis 9.5
1069 invasive aspergillosis 9.5
1070 adenoiditis 9.5
1071 swine influenza 9.5
1072 foodborne botulism 9.5
1073 periventricular nodular heterotopia 9.5
1074 early congenital syphilis 9.5
1075 exanthema subitum 9.5
1076 adult t-cell leukemia 9.5
1077 tooth agenesis 9.5
1078 funisitis 9.5
1079 peripheral t-cell lymphoma 9.5
1080 t-cell large granular lymphocyte leukemia 9.5
1081 rheumatic heart disease 9.5
1082 peripheral artery disease 9.5
1083 oculogyric crisis 9.5
1084 sleep apnea 9.5
1085 chronic venous insufficiency 9.5
1086 renal fibrosis 9.5
1087 colorectal adenocarcinoma 9.5
1088 arteritic anterior ischemic optic neuropathy 9.5
1089 townes-brocks syndrome 9.5
1090 tonsil squamous cell carcinoma 9.5
1091 mucosal melanoma 9.5
1092 cutaneous t cell lymphoma 9.5
1093 apraxia 9.5
1094 ileitis 9.5
1095 agraphia 9.5
1096 dyschromatosis universalis hereditaria 9.5
1097 persistent generalized lymphadenopathy 9.5
1098 lung abscess 9.5
1099 umbilical hernia 9.5
1100 glucocorticoid-induced osteoporosis 9.5
1101 metal allergy 9.5
1102 salmonellosis 9.5
1103 miyoshi muscular dystrophy 9.5
1104 myoglobinuria 9.5
1105 cytomegalovirus retinitis 9.5
1106 hepatic veno-occlusive disease 9.5
1107 acquired generalized lipodystrophy 9.5
1108 polycystic kidney disease 9.5
1109 mucolipidosis 9.5
1110 thyroid gland anaplastic carcinoma 9.5
1111 myxofibrosarcoma 9.5
1112 non-alcoholic steatohepatitis 9.5
1113 split hand-foot malformation 9.5
1114 venous insufficiency 9.5
1115 xerophthalmia 9.5
1116 osteonecrosis 9.5
1117 neuroretinitis 9.5
1118 louping ill 9.5
1119 left bundle branch hemiblock 9.5
1120 parotitis 9.5
1121 sialadenitis 9.5
1122 siderosis 9.5
1123 prolymphocytic leukemia 9.5
1124 legionellosis 9.5
1125 esophageal atresia 9.5
1126 viral pneumonia 9.5
1127 microinvasive gastric cancer 9.5
1128 osteomalacia 9.5
1129 leukodystrophy 9.5
1130 tropical sprue 9.5
1131 protein-losing enteropathy 9.5
1132 renal hypertension 9.5
1133 mesenteric lymphadenitis 9.5
1134 intracranial aneurysm 9.5
1135 discitis 9.5
1136 corneal edema 9.5
1137 meconium aspiration syndrome 9.5
1138 placenta praevia 9.5
1139 q fever 9.5
1140 bartonellosis 9.5
1141 henoch-schoenlein purpura 9.5
1142 hypoparathyroidism 9.5
1143 allergic conjunctivitis 9.5
1144 neonatal anemia 9.5
1145 arteriovenous malformation 9.5
1146 mobitz type ii atrioventricular block 9.5
1147 lemierre's syndrome 9.5
1148 phlebotomus fever 9.5
1149 megacolon 9.5
1150 epidural abscess 9.5
1151 xanthogranulomatous pyelonephritis 9.5
1152 listeriosis 9.5
1153 cauda equina syndrome 9.5
1154 patau syndrome 9.5
1155 neonatal diabetes mellitus 9.5
1156 choledocholithiasis 9.5
1157 ecthyma 9.5
1158 esophagitis 9.5
1159 pulmonary alveolar proteinosis 9.5
1160 aseptic meningitis 9.5
1161 oligohydramnios 9.5
1162 alcoholic hepatitis 9.5
1163 bronchopneumonia 9.5
1164 leiomyoma 9.5
1165 newborn respiratory distress syndrome 9.5
1166 keratoconjunctivitis sicca 9.5
1167 plasmodium ovale malaria 9.5
1168 hereditary spherocytosis 9.5
1169 leukostasis 9.5
1170 dementia 9.5
1171 intestinal tuberculosis 9.5
1172 congenital dyserythropoietic anemia 9.5
1173 skin sarcoidosis 9.5
1174 cardiac sarcoidosis 9.5
1175 congenital hypoplastic anemia 9.5
1176 splenic artery aneurysm 9.5
1177 algoneurodystrophy 9.5
1178 autoimmune polyendocrine syndrome 9.5
1179 sclerosing cholangitis 9.5
1180 ascending cholangitis 9.5
1181 pyuria 9.5
1182 gonadal dysgenesis 9.5
1183 pemphigoid gestationis 9.5
1184 glossitis 9.5
1185 labyrinthitis 9.5
1186 cholera 9.5
1187 rheumatic fever 9.5
1188 keratosis 9.5
1189 chronic cystitis 9.5
1190 neuroendocrine tumor 9.5
1191 ichthyosis 9.5
1192 retinal vein occlusion 9.5
1193 factitious disorder 9.5
1194 toxic megacolon 9.5
1195 neuroendocrine carcinoma 9.5
1196 status epilepticus 9.5
1197 epilepsy 9.5
1198 mononeuritis multiplex 9.5
1199 hyperuricemia 9.5
1200 bardet-biedl syndrome 9.5
1201 encephalomalacia 9.5
1202 constipation 9.5
1203 b cell deficiency 9.5
1204 ectodermal dysplasia 9.5
1205 ascending colon cancer 9.5
1206 factor xiii deficiency 9.5
1207 lateral sclerosis 9.5
1208 nocardiosis 9.5
1209 dyspepsia 9.5
1210 arteriosclerosis 9.5
1211 retinal vascular disease 9.5
1212 sensory peripheral neuropathy 9.5
1213 transverse colon cancer 9.5
1214 kidney cancer 9.5
1215 cystic teratoma 9.5
1216 adenofibroma 9.5
1217 acrodermatitis 9.5
1218 epidermolysis bullosa 9.5
1219 contact dermatitis 9.5
1220 rectosigmoid cancer 9.5
1221 bronchiolitis obliterans 9.5
1222 middle lobe syndrome 9.5
1223 acalculous cholecystitis 9.5
1224 long qt syndrome 9.5
1225 endometrial adenocarcinoma 9.5
1226 cervix carcinoma 9.5
1227 immune system disease 9.5
1228 hypersensitivity reaction type iv disease 9.5
1229 newcastle disease 9.5
1230 bronchiolitis 9.5
1231 cockayne syndrome 9.5
1232 lobular neoplasia 9.5
1233 allergic contact dermatitis 9.5
1234 food allergy 9.5
1235 astrocytoma 9.5
1236 malignant glioma 9.5
1237 cystic lymphangioma 9.5
1238 gingivitis 9.5
1239 lipomatosis 9.5
1240 oligodendroglioma 9.5
1241 lysosomal storage disease 9.5
1242 pleomorphic rhabdomyosarcoma 9.5
1243 inappropriate adh syndrome 9.5
1244 carotid artery thrombosis 9.5
1245 mammary paget's disease 9.5
1246 turner syndrome 9.5
1247 signet ring cell adenocarcinoma 9.5
1248 retinitis 9.5
1249 gastric adenocarcinoma 9.5
1250 hermansky-pudlak syndrome 9.5
1251 pleural empyema 9.5
1252 porokeratosis 9.5
1253 shwartzman phenomenon 9.5
1254 craniopharyngioma 9.5
1255 bartholin's gland carcinoma 9.5
1256 multidrug-resistant tuberculosis 9.5
1257 tricuspid valve insufficiency 9.5
1258 agnosia 9.5
1259 primary syphilis 9.5
1260 rh isoimmunization 9.5
1261 hyperglycemia 9.5
1262 histiocytoma 9.5
1263 polyradiculopathy 9.5
1264 epidermolysis bullosa acquisita 9.5
1265 erdheim-chester disease 9.5
1266 myofibroma 9.5
1267 cutaneous fibrous histiocytoma 9.5
1268 juvenile xanthogranuloma 9.5
1269 dysgerminoma 9.5
1270 breast angiosarcoma 9.5
1271 dysgraphia 9.5
1272 intestinal benign neoplasm 9.5
1273 gastric neuroendocrine neoplasm 9.5
1274 extragonadal germ cell cancer 9.5
1275 brain edema 9.5
1276 calciphylaxis 9.5
1277 placenta accreta 9.5
1278 anti-basement membrane glomerulonephritis 9.5
1279 benign ependymoma 9.5
1280 pilocytic astrocytoma of cerebellum 9.5
1281 colorado tick fever 9.5
1282 lymph node tuberculosis 9.5
1283 tubular adenocarcinoma 9.5
1284 pericardial tuberculosis 9.5
1285 myelodysplastic/myeloproliferative neoplasm 9.5
1286 alcoholic pancreatitis 9.5
1287 ovarian cystic teratoma 9.5
1288 demyelinating polyneuropathy 9.5
1289 gastric leiomyosarcoma 9.5
1290 blepharospasm 9.5
1291 anterograde amnesia 9.5
1292 hemoglobin d disease 9.5
1293 paget's disease of bone 9.5
1294 schizoaffective disorder 9.5
1295 dystonia 9.5
1296 mature teratoma 9.5
1297 chiasmal syndrome 9.5
1298 pleomorphic carcinoma 9.5
1299 adrenal neuroblastoma 9.5
1300 adenosine deaminase deficiency 9.5
1301 apical myocardial infarction 9.5
1302 subendocardial myocardial infarction 9.5
1303 posterolateral myocardial infarction 9.5
1304 lateral myocardial infarction 9.5
1305 silent myocardial infarction 9.5
1306 anteroseptal myocardial infarction 9.5
1307 eosinophilic pneumonia 9.5
1308 mitral valve disease 9.5
1309 bronchitis 9.5
1310 reactive arthritis 9.5
1311 thyroid hyalinizing trabecular adenoma 9.5
1312 inflammatory breast carcinoma 9.5
1313 corpus callosum lipoma 9.5
1314 acute disseminated encephalomyelitis 9.5
1315 double outlet right ventricle 9.5
1316 pulmonary valve stenosis 9.5
1317 skin tag 9.5
1318 mature b-cell neoplasm 9.5
1319 sarcomatosis 9.5
1320 macular holes 9.5
1321 muscular atrophy 9.5
1322 gastrointestinal system disease 9.5
1323 delusional disorder 9.5
1324 placenta disease 9.5
1325 hemarthrosis 9.5
1326 carotid artery occlusion 9.5
1327 septic arthritis 9.5
1328 periodontitis 9.5
1329 intestinal obstruction 9.5
1330 ileus 9.5
1331 intestinal volvulus 9.5
1332 mucormycosis 9.5
1333 polyhydramnios 9.5
1334 chronic fatigue syndrome 9.5
1335 genital herpes 9.5
1336 in situ carcinoma 9.5
1337 bacterial pneumonia 9.5
1338 dermatophytosis 9.5
1339 atrophic gastritis 9.5
1340 sideroblastic anemia 9.5
1341 autosomal dominant polycystic kidney disease 9.5
1342 hepatopulmonary syndrome 9.5
1343 pityriasis versicolor 9.5
1344 leishmaniasis 9.5
1345 cutaneous leishmaniasis 9.5
1346 gas gangrene 9.5
1347 pemphigus 9.5
1348 erythromelalgia 9.5
1349 homocystinuria 9.5
1350 priapism 9.5
1351 lymphangitis 9.5
1352 status asthmaticus 9.5
1353 exophthalmos 9.5
1354 hypopituitarism 9.5
1355 hypertensive encephalopathy 9.5
1356 intracranial hypertension 9.5
1357 lipid storage disease 9.5
1358 senile cataract 9.5
1359 pulmonary emphysema 9.5
1360 biliary tract disease 9.5
1361 omsk hemorrhagic fever 9.5
1362 baraitser-winter cerebrofrontofacial syndrome 9.5
1363 congenital disorders of n-linked glycosylation and multiple pathway 9.5
1364 acute leukemia of ambiguous lineage 9.5
1365 aminoaciduria 9.5
1366 angioimmunoblastic lymphadenopathy with dysproteinemia 9.5
1367 angiosarcoma of the scalp 9.5
1368 arachnoid cysts 9.5
1369 asherman's syndrome 9.5
1370 autoimmune myocarditis 9.5
1371 bone marrow necrosis 9.5
1372 broken heart syndrome 9.5
1373 bronchopulmonary dysplasia 9.5
1374 chromosome 4p deletion 9.5
1375 chronic inflammatory demyelinating polyneuropathy 9.5
1376 congenital human immunodeficiency virus 9.5
1377 congenital mumps 9.5
1378 cutaneous sclerosis 9.5
1379 dandy-walker complex 9.5
1380 dextrocardia with situs inversus 9.5
1381 diffuse neonatal hemangiomatosis 9.5
1382 dysfibrinogenemia 9.5
1383 eisenmenger syndrome 9.5
1384 eosinophilic granulomatosis with polyangiitis 9.5
1385 ependymoma 9.5
1386 exfoliative dermatitis 9.5
1387 fasting hypoglycemia 9.5
1388 fournier gangrene 9.5
1389 gianotti crosti syndrome 9.5
1390 glucagonoma 9.5
1391 growth hormone deficiency 9.5
1392 hemoglobinemia 9.5
1393 idiopathic neutropenia 9.5
1394 lathyrism 9.5
1395 laugier-hunziker syndrome 9.5
1396 lrba deficiency 9.5
1397 lymphatic malformations 9.5
1398 meningococcal infection 9.5
1399 meningoencephalocele 9.5
1400 mercury poisoning 9.5
1401 mollaret meningitis 9.5
1402 mullerian aplasia 9.5
1403 myelodysplastic syndrome with excess blasts 9.5
1404 nephrogenic systemic fibrosis 9.5
1405 nonseminomatous germ cell tumor 9.5
1406 orbital lymphangioma 9.5
1407 paroxysmal cold hemoglobinuria 9.5
1408 pemphigus foliaceus 9.5
1409 pigmented purpuric dermatosis 9.5
1410 pilocytic astrocytoma 9.5
1411 polymyositis 9.5
1412 primary effusion lymphoma 9.5
1413 pure autonomic failure 9.5
1414 pustular psoriasis 9.5
1415 refractory cytopenia with unilineage dysplasia 9.5
1416 reticuloendotheliosis 9.5
1417 ring chromosome 21 9.5
1418 rosai-dorfman disease 9.5
1419 scleromyxedema 9.5
1420 shapiro syndrome 9.5
1421 sickle beta thalassemia 9.5
1422 single ventricular heart 9.5
1423 stevens-johnson syndrome/toxic epidermal necrolysis 9.5
1424 superficial siderosis of the central nervous system 9.5
1425 transposition of the great arteries 9.5
1426 transverse myelitis 9.5
1427 triploidy 9.5
1428 tuberculous meningitis 9.5
1429 undifferentiated connective tissue disease 9.5
1430 virus associated hemophagocytic syndrome 9.5
1431 cryptogenic cirrhosis 9.5
1432 isolated pierre robin sequence 9.5
1433 autonomic dysfunction 9.5
1434 cavernous malformation 9.5
1435 cerebral atrophy 9.5
1436 myoclonus 9.5
1437 paresthesia 9.5
1438 spasticity 9.5
1439 immuno-osseous dysplasia 9.5
1440 mixed germ cell tumor 9.5
1441 obsolete: heinz body anemia 9.5
1442 t-cell non-hodgkin lymphoma 9.5
1443 differentiated thyroid carcinoma 9.5
1444 endotheliitis 9.5
1445 epithelioid hemangioendothelioma 9.5
1446 hemimelia 9.5
1447 hemophagocytic syndrome associated with an infection 9.5
1448 secondary hemophagocytic lymphohistiocytosis 9.5
1449 superficial siderosis 9.5
1450 autosomal recessive malignant osteopetrosis 9.5
1451 occipital encephalocele 9.5
1452 pulmonary arterial hypertension associated with portal hypertension 9.5
1453 autoimmune polyendocrinopathy type 4 9.5
1454 virus-associated trichodysplasia spinulosa 9.5
1455 acute pandysautonomia 9.5
1456 bilateral massive adrenal hemorrhage 9.5
1457 ring chromosome 9.5
1458 fixed drug eruption 9.5
1459 epstein-barr virus-associated malignant lymphoproliferative disorder 9.5
1460 neonatal lupus erythematosus 9.5
1461 neonatal dermatomyositis 9.5
1462 secondary sclerosing cholangitis 9.5
1463 acquired prothrombin deficiency 9.5
1464 longitudinal limb defect 9.5
1465 digitalis poisoning 9.5
1466 congenital amyoplasia 9.5
1467 benign idiopathic neonatal seizures 9.5
1468 recurrent acute pancreatitis 9.5
1469 classic hairy cell leukemia 9.5
1470 rare chromosomal anomaly 9.5
1471 moderate and severe traumatic brain injury 9.5
1472 mixed-type autoimmune hemolytic anemia 9.5
1473 autoimmune hemolytic anemia, warm type 9.5
1474 lymphedema 9.5
1475 erythrokeratoderma 9.5
1476 x-linked intellectual disability-macrocephaly-macroorchidism syndrome 9.5
1477 primary hypophysitis 9.5
1478 light and heavy chain deposition disease 9.5
1479 heavy chain deposition disease 9.5
1480 rare coagulation disorder 9.5
1481 rickettsial disease 9.5
1482 aregenerative anemia 9.5
1483 streptococcal toxic-shock syndrome 9.5
1484 acute megakaryoblastic leukemia in down syndrome 9.5
1485 inherited blood coagulation disease 9.3 ITGB3 ITGA2B GP9 GP1BB GP1BA
1486 blood coagulation disease 8.5 MYH9 MPL ITGB3 ITGA2B GP9 GP1BB

Graphical network of the top 20 diseases related to Thrombocytopenia:



Diseases related to Thrombocytopenia

Symptoms & Phenotypes for Thrombocytopenia

MGI Mouse Phenotypes related to Thrombocytopenia:

46 (showing 5, show less)
# Description MGI Source Accession Score Top Affiliating Genes
1 cellular MP:0005384 10.13 CYCS ETV6 GATA1 GP1BA HOXA11 ITGA2
2 hematopoietic system MP:0005397 9.97 ADAMTS13 CYCS ETV6 GATA1 GP1BA GP1BB
3 embryo MP:0005380 9.86 CYCS ETV6 GATA1 ITGA2B ITGB3 MASTL
4 homeostasis/metabolism MP:0005376 9.73 ADAMTS13 ANKRD26 ETV6 GATA1 GP1BA GP1BB
5 immune system MP:0005387 9.28 ADAMTS13 CYCS ETV6 GATA1 ITGA2B ITGB3

Drugs & Therapeutics for Thrombocytopenia

PubMed Health treatment related to Thrombocytopenia: 63

Treatment for thrombocytopenia depends on its cause and severity. The main goal of treatment is to prevent death and disability caused by bleeding. If your condition is mild, you may not need treatment. A fully normal platelet count isn't necessary to prevent bleeding, even with severe cuts or accidents. Thrombocytopenia often improves when its underlying cause is treated. People who inherit the condition usually don't need treatment. If a reaction to a medicine is causing a low platelet count, your doctor may prescribe another medicine. Most people recover after the initial medicine has been stopped. For heparin-induced thrombocytopenia (HIT), stopping the heparin isn't enough. Often, you'll need another medicine to prevent blood clotting. If your immune system is causing a low platelet count, your doctor may prescribe medicines to suppress the immune system.

Drugs for Thrombocytopenia (from DrugBank, HMDB, Dgidb, PharmGKB, IUPHAR, NovoSeek, BitterDB):

(showing 552, show less)
# Name Status Phase Clinical Trials Cas Number PubChem Id
1
Bivalirudin Approved, Investigational Phase 4 128270-60-0 16129704
2
Oprelvekin Approved, Investigational Phase 4 145941-26-0
3
Hydroxychloroquine Approved Phase 4 118-42-3 3652
4
Sodium citrate Approved, Investigational Phase 4 68-04-2
5
Atorvastatin Approved Phase 4 134523-00-5 60823
6
Hydrocortisone Approved, Vet_approved Phase 4 50-23-7 5754
7
Hydrocortisone acetate Approved, Vet_approved Phase 4 50-03-3
8
Peginterferon alfa-2b Approved Phase 4 99210-65-8, 215647-85-1
9
Ethinyl Estradiol Approved Phase 4 57-63-6 5991
10
Estradiol Approved, Investigational, Vet_approved Phase 4 50-28-2 5757
11
Polyestradiol phosphate Approved Phase 4 28014-46-2
12
Bupivacaine Approved, Investigational Phase 4 2180-92-9, 38396-39-3 2474
13
Acetaminophen Approved Phase 4 103-90-2 1983
14
Phylloquinone Approved, Investigational Phase 4 84-80-0
15
Abciximab Approved Phase 4 143653-53-6
16
Cefpirome Approved Phase 4 84957-29-9 5479539
17
Moxifloxacin Approved, Investigational Phase 4 354812-41-2, 151096-09-2 152946
18
Norgestimate Approved, Investigational Phase 4 35189-28-7 6540478
19
Tirofiban Approved Phase 4 144494-65-5 60947
20
Acenocoumarol Approved, Investigational Phase 4 152-72-7 9052 54676537
21 Bemiparin Approved, Investigational Phase 4 91449-79-5
22
Ketorolac Approved Phase 4 74103-06-3, 66635-83-4 3826
23
Pancrelipase Approved, Investigational Phase 4 53608-75-6
24
Phenytoin Approved, Vet_approved Phase 4 57-41-0 1775
25
glycyrrhizin Approved, Experimental Phase 4 1405-86-3 3495