MCID: THR014
MIFTS: 68

Thrombocytopenia

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

Aliases & Classifications for Thrombocytopenia

Summaries for Thrombocytopenia

KEGG : 36 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 due to platelet alloimmunization and thrombocytopenia 1. An important gene associated with Thrombocytopenia is ANKRD26 (Ankyrin Repeat Domain 26), 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 Reduced mammosphere formation and cellular

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

PubMed Health : 62 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 : 74 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 Ankrd26-Related Thrombocytopenia
Myh9 Related Thrombocytopenia

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

(showing 1499, show less)
# Related Disease Score Top Affiliating Genes
1 thrombocytopenia due to platelet alloimmunization 35.6 MPL ITGB3 ITGA2B ITGA2 GP9 ANKRD26
2 thrombocytopenia 1 35.6 WAS HOXA11 GATA1
3 fetal and neonatal alloimmune thrombocytopenia 35.4 ITGB3 ITGA2B ITGA2 GP1BB GP1BA
4 amegakaryocytic thrombocytopenia, congenital 35.4 RBM8A MPL GATA1
5 acquired thrombocytopenia 35.1 MYH9 MPL ITGB3 IL11 GP1BB
6 thrombocytopenia 2 35.0 MASTL ANKRD26
7 primary thrombocytopenia 35.0 MPL ITGB3 ITGA2B GP1BA ADAMTS13
8 thrombocytopenic purpura, autoimmune 34.8 MPL ITGB3 ITGA2B IL11 GP1BA ADAMTS13
9 myh-9 related disease 34.8 MYH9 MPL GP9 GP1BB GP1BA ANKRD26
10 thrombocytopenia-absent radius syndrome 34.6 RBM8A ANKRD26
11 ankrd26-related thrombocytopenia 34.6 MYH9 ANKRD26
12 autosomal thrombocytopenia with normal platelets 34.5 MASTL CYCS
13 bernard-soulier syndrome 34.5 MYH9 ITGB3 ITGA2B ITGA2 GP9 GP1BB
14 platelet disorder, familial, with associated myeloid malignancy 34.2 RUNX1 ETV6 ANKRD26
15 blood platelet disease 33.8 WAS RUNX1 MYH9 MPL ITGB3 ITGA2B
16 gray platelet syndrome 33.6 MASTL ITGA2B GP9 GATA1
17 pseudo-von willebrand disease 33.5 GP9 GP1BB GP1BA GATA1
18 purpura 33.0 MPL ITGB3 ITGA2B GP1BA ADAMTS13
19 thrombosis 32.6 MPL ITGB3 ITGA2B ITGA2 GP1BA ADAMTS13
20 acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) 32.5 RUNX1 ETV6
21 autosomal dominant macrothrombocytopenia 32.5 MYH9 ITGB3 ITGA2B GP1BB GP1BA ACTN1
22 myelodysplastic syndrome 32.4 RUNX1 MPL ITGA2B IL11 GATA1 ETV6
23 deficiency anemia 32.4 MPL IL11 GP1BA GATA1 ADAMTS13
24 aplastic anemia 32.1 MPL ITGB3 ITGA2B IL11 GATA1
25 leukemia, acute myeloid 32.0 RUNX1 MPL ITGB3 ITGA2B GATA1 ETV6
26 von willebrand's disease 32.0 ITGB3 ITGA2 GP9 GP1BA ADAMTS13
27 bleeding disorder, platelet-type, 16 32.0 ITGB3 ITGA2B
28 essential thrombocythemia 31.8 MPL ITGB3 ITGA2B IL11 GP1BA GATA1
29 myelofibrosis 31.8 RUNX1 MPL GATA1 ETV6
30 splenic sequestration 31.7 MPL ITGA2B ADAMTS13
31 thrombasthenia 31.7 ITGB3 ITGA2B ITGA2 GP9 GP1BA
32 leukemia, chronic myeloid 31.5 RUNX1 MPL ITGB3 IL11 GATA1 ETV6
33 myeloproliferative neoplasm 31.5 RUNX1 MPL ITGB3 GATA1 ETV6
34 cerebrovascular disease 31.5 ITGB3 ITGA2B ITGA2 GP1BA ADAMTS13
35 glanzmann thrombasthenia 31.5 ITGB3 ITGA2B ITGA2 GP9 GP1BA
36 myocardial infarction 31.4 ITGB3 ITGA2B ITGA2 GP1BA CYCS ADAMTS13
37 coronary thrombosis 31.3 ITGB3 ITGA2B GP1BA
38 megakaryocytic leukemia 30.9 RUNX1 ITGB3 ITGA2B IL11 GATA1
39 refractory anemia 30.9 RUNX1 MPL
40 chronic myelomonocytic leukemia 30.8 RUNX1 MPL ETV6
41 hematologic cancer 30.8 RUNX1 MPL IL11 ETV6 CYCS
42 qualitative platelet defect 30.8 ITGA2B GP1BA
43 velocardiofacial syndrome 30.5 GP9 GP1BB GP1BA
44 aspirin resistance 30.5 ITGB3 ITGA2
45 arteritic anterior ischemic optic neuropathy 30.4 ITGB3 GP1BA
46 heparin-induced thrombocytopenia 12.7
47 thrombocytopenia with beta-thalassemia, x-linked 12.7
48 thrombocytopenia, paris-trousseau type 12.6
49 dyserythropoietic anemia and thrombocytopenia 12.6
50 thrombocytopenia, x-linked, with or without dyserythropoietic anemia 12.6
51 thrombocytopenia 5 12.6
52 radioulnar synostosis with amegakaryocytic thrombocytopenia 1 12.6
53 thrombocytopenia 3 12.6
54 thrombocytopenia 4 12.6
55 hemangioma-thrombocytopenia syndrome 12.5
56 thrombocytopenia 6 12.5
57 radioulnar synostosis with amegakaryocytic thrombocytopenia 2 12.5
58 acquired amegakaryocytic thrombocytopenia 12.5
59 thrombocytopenia, anemia, and myelofibrosis 12.5
60 radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome 12.4
61 myh9 related thrombocytopenia 12.4
62 transient neonatal thrombocytopenia 12.4
63 multifocal lymphangioendotheliomatosis with thrombocytopenia 12.3
64 thrombocytopenia, cyclic 12.3
65 hereditary thrombocytopenia with normal platelets 12.3
66 thrombocytopenia robin sequence 12.2
67 thrombocytopenia with elevated serum iga and renal disease 12.2
68 wiskott-aldrich syndrome 12.2
69 osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension 12.2
70 congenital autosomal recessive small-platelet thrombocytopenia 12.2
71 rare hemorrhagic disorder due to a constitutional thrombocytopenia 12.1
72 isolated constitutional thrombocytopenia 12.1
73 ivic syndrome 12.1
74 macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss 12.0
75 autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome 12.0
76 syndromic constitutional thrombocytopenia 12.0
77 obsolete: hereditary thrombocytopenia-hematological cancer predisposition syndrome 12.0
78 bleeding disorder, platelet-type, 17 12.0
79 thrombotic thrombocytopenic purpura 12.0
80 bleeding disorder, platelet-type, 20 11.9
81 dk phocomelia syndrome 11.9
82 evans' syndrome 11.9
83 deafness, autosomal dominant 1 11.8
84 hemolytic-uremic syndrome 11.8
85 hemolytic uremic syndrome, atypical 1 11.7
86 anemia, x-linked, with or without neutropenia and/or platelet abnormalities 11.6
87 autoimmune lymphoproliferative syndrome 11.6
88 jacobsen syndrome 11.5
89 thrombotic thrombocytopenic purpura, congenital 11.5
90 tau syndrome 11.5
91 sea-blue histiocyte disease 11.5
92 immunodysregulation, polyendocrinopathy, and enteropathy, x-linked 11.5
93 pearson marrow-pancreas syndrome 11.5
94 leukemia, acute lymphoblastic 11.4
95 digeorge syndrome 11.4
96 shwachman-diamond syndrome 1 11.4
97 bleeding disorder, platelet-type, 21 11.4
98 antiphospholipid syndrome 11.4
99 tafro syndrome 11.4
100 forsythe-wakeling syndrome 11.4
101 faye-petersen-ward-carey syndrome 11.4
102 dengue disease 11.3
103 thrombotic microangiopathy 11.3
104 bleeding disorder, platelet-type, 19 11.3
105 acute leukemia 11.3
106 dengue hemorrhagic fever 11.3
107 dengue virus 11.3
108 myeloma, multiple 11.3
109 gaucher's disease 11.3
110 severe pre-eclampsia 11.3
111 macrothrombocytopenia, autosomal dominant, tubb1-related 11.3
112 common variable immunodeficiency 11.3
113 viral hemorrhagic fever 11.3
114 stormorken syndrome 11.3
115 fanconi anemia, complementation group a 11.3
116 rare hemorrhagic disorder due to a platelet anomaly 11.3
117 rare hemorrhagic disorder due to an acquired platelet anomaly 11.3
118 rare hemorrhagic disorder due to a constitutional platelet anomaly 11.3
119 langerhans cell histiocytosis 11.3
120 acute promyelocytic leukemia 11.3
121 platelet glycoprotein iv deficiency 11.3
122 proteasome-associated autoinflammatory syndrome 1 11.3
123 dyskeratosis congenita 11.3
124 littoral cell angioma of the spleen 11.3
125 angioma, tufted 11.3
126 takenouchi-kosaki syndrome 11.3
127 t-cell large granular lymphocyte leukemia 11.3
128 niemann-pick disease 11.3
129 niemann-pick disease, type b 11.3
130 bleeding disorder, platelet-type, 9 11.3
131 bone marrow failure syndrome 4 11.3
132 thrombotic thrombocytopenic purpura, acquired 11.3
133 blood coagulation disease 11.1 WAS MYH9 MPL ITGB3 ITGA2B IL11
134 antiphospholipid syndrome, familial 11.1
135 bernard-soulier syndrome, type a2, autosomal dominant 11.1
136 aicardi-goutieres syndrome 1 11.1
137 osteopetrosis, autosomal recessive 5 11.1
138 tn polyagglutination syndrome 11.1
139 propionic acidemia 11.1
140 cerebroretinal microangiopathy with calcifications and cysts 1 11.1
141 nephrotic syndrome, type 7 11.1
142 autoimmune lymphoproliferative syndrome, type v 11.1
143 pseudo-torch syndrome 2 11.1
144 proteasome-associated autoinflammatory syndrome 3 11.1
145 inherited blood coagulation disease 11.0 ITGB3 ITGA2B ITGA2 GP9 GP1BB GP1BA
146 myeloproliferative syndrome, transient 11.0 MPL ITGB3 ITGA2B GP1BA GATA1
147 ataxia-pancytopenia syndrome 10.9
148 storage pool platelet disease 10.9
149 folate malabsorption, hereditary 10.9
150 gaucher disease, type iii 10.9
151 pseudo-torch syndrome 1 10.9
152 dihydropyrimidine dehydrogenase deficiency 10.9
153 autoimmune lymphoproliferative syndrome, type iia 10.9
154 transaldolase deficiency 10.9
155 griscelli syndrome, type 2 10.9
156 spondyloenchondrodysplasia with immune dysregulation 10.9
157 gaucher disease, perinatal lethal 10.9
158 congenital disorder of glycosylation, type ih 10.9
159 aicardi-goutieres syndrome 2 10.9
160 aicardi-goutieres syndrome 3 10.9
161 aicardi-goutieres syndrome 4 10.9
162 thiopurines, poor metabolism of, 1 10.9
163 immunodeficiency 10 10.9
164 hemolytic uremic syndrome, atypical 2 10.9
165 hemolytic uremic syndrome, atypical 3 10.9
166 hemolytic uremic syndrome, atypical 4 10.9
167 hemolytic uremic syndrome, atypical 5 10.9
168 hemolytic uremic syndrome, atypical 6 10.9
169 aicardi-goutieres syndrome 5 10.9
170 lymphoproliferative syndrome 1 10.9
171 wiskott-aldrich syndrome 2 10.9
172 leukoencephalopathy, brain calcifications, and cysts 10.9
173 aicardi-goutieres syndrome 6 10.9
174 aicardi-goutieres syndrome 7 10.9
175 epilepsy, hearing loss, and mental retardation syndrome 10.9
176 immunodeficiency 46 10.9
177 mirage syndrome 10.9
178 platelet abnormalities with eosinophilia and immune-mediated inflammatory disease 10.9
179 shwachman-diamond syndrome 2 10.9
180 argentine hemorrhagic fever 10.9
181 alkhurma hemorrhagic fever 10.9
182 aicardi-goutieres syndrome 10.9
183 congenital toxoplasmosis 10.9
184 acute myeloblastic leukemia with maturation 10.9
185 acute myeloblastic leukemia without maturation 10.9
186 fibular hemimelia 10.9
187 hemolytic uremic syndrome, atypical, childhood 10.9
188 core binding factor acute myeloid leukemia 10.9
189 cytogenetically normal acute myeloid leukemia 10.9
190 familial acute myeloid leukemia with mutated cebpa 10.9
191 autoimmune disease of blood 10.9 MPL ITGB3 ITGA2B ADAMTS13
192 malignant gastric germ cell tumor 10.8 ITGB3 ITGA2B
193 acute basophilic leukemia 10.8 GATA1 ETV6
194 neutropenia 10.8
195 autoimmune disease 10.7
196 gastric teratoma 10.7 ITGB3 ITGA2B
197 submucous uterine fibroid 10.7 IL11 HOXA11
198 hemolytic anemia 10.7
199 thrombophilia due to thrombin defect 10.7
200 disseminated intravascular coagulation 10.6
201 acquired von willebrand syndrome 10.6 GP1BA ADAMTS13
202 systemic lupus erythematosus 10.6
203 lupus erythematosus 10.6
204 pulmonary embolism 10.6
205 splenomegaly 10.6
206 liver cirrhosis 10.6
207 liver disease 10.6
208 cebpa-associated familial acute myeloid leukemia 10.5 RUNX1 ETV6
209 thrombocytosis 10.5
210 pre-eclampsia 10.5
211 hepatitis c 10.5
212 hypersplenism 10.5
213 immune deficiency disease 10.5
214 pulmonary fibrosis and/or bone marrow failure, telomere-related, 2 10.5
215 occlusion precerebral artery 10.5 ITGA2B CYCS
216 kidney disease 10.5
217 acute kidney failure 10.5
218 lymphocytic leukemia 10.5
219 ischemia 10.5
220 malaria 10.4
221 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 10.4
222 hemangioma 10.4
223 exanthem 10.4
224 portal hypertension 10.4
225 pancytopenia 10.4
226 anemia, autoimmune hemolytic 10.4
227 hepatitis c virus 10.4
228 granulocytopenia 10.4
229 leukemia, chronic lymphocytic 10.4
230 sarcoidosis 1 10.3
231 leukemia 10.3
232 dermatitis 10.3
233 myeloid leukemia 10.3
234 eclampsia 10.3
235 pfeiffer syndrome 10.3
236 hellp syndrome 10.3
237 hemophilia 10.3
238 toxic shock syndrome 10.3
239 chickenpox 10.3
240 enterocolitis 10.3
241 endocarditis 10.3
242 respiratory failure 10.3
243 diarrhea 10.3
244 hepatitis 10.3
245 acquired immunodeficiency syndrome 10.3
246 end stage renal failure 10.3
247 cytomegalovirus infection 10.3
248 iron metabolism disease 10.3
249 graft-versus-host disease 10.2
250 lymphopenia 10.2
251 vasculitis 10.2
252 perinatal necrotizing enterocolitis 10.2
253 glomerulonephritis 10.2
254 polycythemia 10.2
255 rubella 10.2
256 plasmodium vivax malaria 10.2
257 intermediate coronary syndrome 10.2
258 47,xyy 10.2
259 hepatocellular carcinoma 10.2
260 severe combined immunodeficiency 10.2
261 acute myocardial infarction 10.2
262 cytokine deficiency 10.2
263 allergic hypersensitivity disease 10.2
264 connective tissue disease 10.2
265 pulmonary hypertension 10.2
266 limb ischemia 10.2
267 lymphoproliferative syndrome 10.2
268 portal vein thrombosis 10.2
269 iron deficiency anemia 10.2
270 human immunodeficiency virus type 1 10.2
271 thrombophilia 10.2
272 hyperthyroidism 10.2
273 colorectal cancer 10.2
274 macrothrombocytopenia with mitral valve insufficiency 10.2
275 brucellosis 10.2
276 leptospirosis 10.2
277 congestive heart failure 10.2
278 hypereosinophilic syndrome 10.2
279 hemophagocytic lymphohistiocytosis 10.2
280 lymphoma 10.2
281 pulmonary tuberculosis 10.2
282 pneumonia 10.2
283 cardiogenic shock 10.2
284 factor viii deficiency 10.1
285 hemophilia a 10.1
286 autosomal recessive disease 10.1
287 vascular disease 10.1
288 histiocytosis 10.1
289 budd-chiari syndrome 10.1
290 cardiac arrest 10.1
291 bacterial infectious disease 10.1
292 hypothyroidism 10.1
293 hemoglobinuria 10.1
294 varicose veins 10.1
295 helicobacter pylori infection 10.1
296 hepatitis b 10.1
297 b-cell lymphoma 10.1
298 thyroiditis 10.1
299 ulcerative colitis 10.1
300 red cell aplasia 10.1
301 colitis 10.1
302 thalassemia 10.1
303 plasmodium falciparum malaria 10.1
304 systemic scleroderma 10.1
305 giant hemangioma 10.1
306 polycythemia vera 10.1
307 branchiootic syndrome 1 10.1
308 angiosarcoma 10.1
309 epidemic typhus 10.1
310 nephrotic syndrome 10.1
311 graves' disease 10.1
312 pure red-cell aplasia 10.1
313 aortic aneurysm 10.1
314 cataract 10.1
315 measles 10.1
316 48,xyyy 10.1
317 encephalopathy 10.1
318 renal cell carcinoma, nonpapillary 10.1
319 graves disease 1 10.1
320 hydrocephalus 10.1
321 heart disease 10.1
322 synostosis 10.1
323 viral hepatitis 10.1
324 glioblastoma multiforme 10.1
325 encephalitis 10.1
326 gata1-related x-linked cytopenia 10.1
327 aneurysm 10.1
328 down syndrome 10.1
329 lung cancer 10.1
330 gaucher disease, type i 10.1
331 myasthenia gravis 10.1
332 patent ductus arteriosus 1 10.1
333 kawasaki disease 10.1
334 paroxysmal nocturnal hemoglobinuria 10.1
335 scrub typhus 10.1
336 lymphadenitis 10.1
337 heart septal defect 10.1
338 gastritis 10.1
339 pancreatitis 10.1
340 myocarditis 10.1
341 macroglobulinemia 10.1
342 headache 10.1
343 myositis 10.0
344 lymphoma, hodgkin, classic 10.0
345 stroke, ischemic 10.0
346 mycobacterium tuberculosis 1 10.0
347 inflammatory bowel disease 10.0
348 infective endocarditis 10.0
349 mumps 10.0
350 hepatitis a 10.0
351 pustulosis of palm and sole 10.0
352 arthritis 10.0
353 psoriasis 10.0
354 fatty liver disease 10.0
355 chromosomal triplication 10.0
356 phocomelia 10.0
357 aortic aneurysm, familial abdominal, 1 10.0
358 rheumatoid arthritis 10.0
359 scleroderma, familial progressive 10.0
360 vitamin b12 deficiency 10.0
361 esophageal varix 10.0
362 autoimmune hepatitis 10.0
363 relapsing-remitting multiple sclerosis 10.0
364 thrombophlebitis 10.0
365 chronic kidney disease 10.0
366 neuropathy 10.0
367 crohn's disease 10.0
368 hypoglycemia 10.0
369 acute graft versus host disease 10.0
370 rare surgical neurologic disease 10.0
371 ovarian cancer 10.0
372 platelet aggregation, spontaneous 10.0
373 congenital heart defects, hamartomas of tongue, and polysyndactyly 10.0
374 thymoma, familial 10.0
375 peripheral vascular disease 10.0
376 dengue shock syndrome 10.0
377 korean hemorrhagic fever 10.0
378 pain agnosia 10.0
379 hantavirus hemorrhagic fever with renal syndrome 10.0
380 cholestasis 10.0
381 polyneuropathy 10.0
382 mitral valve stenosis 10.0
383 hemorrhagic disease 10.0
384 transient cerebral ischemia 10.0
385 agammaglobulinemia 10.0
386 thymoma 10.0
387 myopathy 10.0
388 compartment syndrome 10.0
389 influenza 10.0
390 subacute delirium 10.0
391 chronic graft versus host disease 10.0
392 hemangioendothelioma 10.0
393 seizure disorder 10.0
394 acute liver failure 10.0
395 kaposi sarcoma 10.0
396 multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 10.0
397 wilms tumor 5 10.0
398 yemenite deaf-blind hypopigmentation syndrome 10.0
399 glucocorticoid resistance, generalized 10.0
400 hydrops, lactic acidosis, and sideroblastic anemia 10.0
401 atrial fibrillation 10.0
402 ehrlichiosis 10.0
403 sarcoma 10.0
404 tetanus 10.0
405 pulmonary edema 10.0
406 visual epilepsy 10.0
407 primary biliary cirrhosis 10.0
408 acute cystitis 10.0
409 typhoid fever 10.0
410 megaloblastic anemia 10.0
411 atrial heart septal defect 10.0
412 bilirubin metabolic disorder 10.0
413 mixed connective tissue disease 10.0
414 placental insufficiency 10.0
415 syphilis 10.0
416 spindle cell sarcoma 10.0
417 uremia 10.0
418 peritonitis 10.0
419 lung disease 10.0
420 was-related disorders 10.0
421 angiomatosis 10.0
422 alcohol dependence 9.9
423 hashimoto thyroiditis 9.9
424 triiodothyronine receptor auxiliary protein 9.9
425 celiac disease 1 9.9
426 ocular motor apraxia 9.9
427 gastric cancer 9.9
428 aspergillosis 9.9
429 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 9.9
430 hyperlipoproteinemia, type iii 9.9
431 bacterial sepsis 9.9
432 tick-borne encephalitis 9.9
433 diffuse large b-cell lymphoma 9.9
434 follicular lymphoma 9.9
435 immunoglobulin alpha deficiency 9.9
436 porencephaly 9.9
437 angioimmunoblastic t-cell lymphoma 9.9
438 castleman disease 9.9
439 trypanosomiasis 9.9
440 spotted fever 9.9
441 coronary artery anomaly 9.9
442 amenorrhea 9.9
443 rectum cancer 9.9
444 splenic infarction 9.9
445 combined t cell and b cell immunodeficiency 9.9
446 active peptic ulcer disease 9.9
447 placental abruption 9.9
448 alopecia 9.9
449 catastrophic antiphospholipid syndrome 9.9
450 rapidly involuting congenital hemangioma 9.9
451 breast cancer 9.9
452 multiple sclerosis 9.9
453 fibrosis of extraocular muscles, congenital, 1 9.9
454 pancreatic cancer 9.9
455 autoimmune pancreatitis 9.9
456 human granulocytic anaplasmosis 9.9
457 mantle cell lymphoma 9.9
458 atrioventricular block 9.9
459 non-alcoholic fatty liver disease 9.9
460 dermatomyositis 9.9
461 malignant hypertension 9.9
462 amnestic disorder 9.9
463 pituitary apoplexy 9.9
464 diphtheria 9.9
465 hemopericardium 9.9
466 cardiac tamponade 9.9
467 mitral valve insufficiency 9.9
468 poems syndrome 9.9
469 alcohol use disorder 9.9
470 acute pancreatitis 9.9
471 protein c deficiency 9.9
472 peripheral nervous system disease 9.9
473 bullous pemphigoid 9.9
474 herpes simplex 9.9
475 viral infectious disease 9.9
476 meningitis 9.9
477 miliary tuberculosis 9.9
478 inherited bone marrow failure syndromes 9.9
479 posttransplant acute limbic encephalitis 9.9
480 arteries, anomalies of 9.9
481 exudative vitreoretinopathy 1 9.9
482 hypercholesterolemia, familial, 1 9.9
483 radioulnar synostosis 9.9
484 small cell cancer of the lung 9.9
485 lymphoma, non-hodgkin, familial 9.9
486 diabetes mellitus, ketosis-prone 9.9
487 lung cancer susceptibility 3 9.9
488 cyanosis, transient neonatal 9.9
489 leukemia, acute lymphoblastic 3 9.9
490 rocky mountain spotted fever 9.9
491 drug allergy 9.9
492 multicentric castleman disease 9.9
493 interstitial nephritis 9.9
494 gastric ulcer 9.9
495 microcephaly 9.9
496 alport syndrome 9.9
497 adult respiratory distress syndrome 9.9
498 pericardial effusion 9.9
499 hemosiderosis 9.9
500 osteopetrosis 9.9
501 polyclonal hypergammaglobulinemia 9.9
502 hemangioma of spleen 9.9
503 hairy cell leukemia 9.9
504 iga glomerulonephritis 9.9
505 adenocarcinoma 9.9
506 lipid metabolism disorder 9.9
507 teratoma 9.9
508 hepatitis e 9.9
509 poliomyelitis 9.9
510 peptic ulcer disease 9.9
511 hodgkin's lymphoma, lymphocytic-histiocytic predominance 9.9
512 malignant histiocytosis 9.9
513 chronic thromboembolic pulmonary hypertension 9.9
514 hypoxia 9.9
515 syncope 9.9
516 traumatic brain injury 9.9
517 tremor 9.9
518 congenital hemangioma 9.9
519 pik3ca-related overgrowth syndrome 9.9
520 refractory cytopenia with multilineage dysplasia 9.9
521 acute adrenal insufficiency 9.9
522 cornelia de lange syndrome 1 9.8
523 erythroleukemia, familial 9.8
524 felty syndrome 9.8
525 migraine with or without aura 1 9.8
526 noonan syndrome 1 9.8
527 pernicious anemia 9.8
528 prostate cancer 9.8
529 pulmonary hypertension, primary, 1 9.8
530 tetralogy of fallot 9.8
531 vitiligo-associated multiple autoimmune disease susceptibility 6 9.8
532 afibrinogenemia, congenital 9.8
533 sjogren syndrome 9.8
534 hemophilia b 9.8
535 ventricular fibrillation, paroxysmal familial, 1 9.8
536 vitiligo-associated multiple autoimmune disease susceptibility 1 9.8
537 pulmonary disease, chronic obstructive 9.8
538 major affective disorder 8 9.8
539 major affective disorder 9 9.8
540 pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis 9.8
541 beta-thalassemia 9.8
542 aortic valve disease 2 9.8
543 encephalopathy, progressive, early-onset, with episodic rhabdomyolysis 9.8
544 angina pectoris 9.8
545 chikungunya 9.8
546 aspiration pneumonia 9.8
547 chorioamnionitis 9.8
548 marginal zone b-cell lymphoma 9.8
549 splenic marginal zone lymphoma 9.8
550 aphasia 9.8
551 ptosis 9.8
552 zika fever 9.8
553 lymphoblastic lymphoma 9.8
554 meningoencephalitis 9.8
555 hemiplegia 9.8
556 asphyxia neonatorum 9.8
557 pyelonephritis 9.8
558 cornelia de lange syndrome 9.8
559 lyme disease 9.8
560 conn's syndrome 9.8
561 acute kidney tubular necrosis 9.8
562 guillain-barre syndrome 9.8
563 acute proliferative glomerulonephritis 9.8
564 coccidioidomycosis 9.8
565 acute poststreptococcal glomerulonephritis 9.8
566 papilledema 9.8
567 lymphangioma 9.8
568 candidiasis 9.8
569 urticaria 9.8
570 pneumothorax 9.8
571 cystitis 9.8
572 pericarditis 9.8
573 cholecystitis 9.8
574 cerebral palsy 9.8
575 gastroenteritis 9.8
576 hemoglobinopathy 9.8
577 cryoglobulinemia 9.8
578 anuria 9.8
579 rhabdomyosarcoma 9.8
580 bipolar disorder 9.8
581 cellulitis 9.8
582 sagittal sinus thrombosis 9.8
583 intracranial thrombosis 9.8
584 juvenile rheumatoid arthritis 9.8
585 collagen disease 9.8
586 diabetes mellitus 9.8
587 bacterial meningitis 9.8
588 babesiosis 9.8
589 toxoplasmosis 9.8
590 acquired hemophilia 9.8
591 acquired hemophilia a 9.8
592 adrenomyeloneuropathy 9.8
593 cold agglutinin disease 9.8
594 congenital rubella 9.8
595 germ cells tumors 9.8
596 pseudo-turner syndrome 9.8
597 back pain 9.8
598 dysphagia 9.8
599 rare hereditary hemochromatosis 9.8
600 histiocytic sarcoma 9.8
601 rare disease in surgical orthopedic 9.8
602 polyploidy 9.8
603 intravascular large b-cell lymphoma 9.8
604 spondyloarthropathy 1 9.8
605 atrial standstill 1 9.8
606 bladder cancer 9.8
607 progressive familial heart block, type ia 9.8
608 cryoglobulinemia, familial mixed 9.8
609 hair whorl 9.8
610 hpa i recognition polymorphism, beta-globin-related 9.8
611 hypertriglyceridemia, familial 9.8
612 osteoporosis 9.8
613 retinal detachment 9.8
614 schistosoma mansoni infection, susceptibility/ 9.8
615 thrombophilia due to activated protein c resistance 9.8
616 cystic fibrosis 9.8
617 hydrops fetalis, nonimmune 9.8
618 roberts syndrome 9.8
619 wilson disease 9.8
620 adrenoleukodystrophy 9.8
621 ataxia and polyneuropathy, adult-onset 9.8
622 anorexia nervosa 9.8
623 creatinine clearance quantitative trait locus 9.8
624 granulomatosis with polyangiitis 9.8
625 bone mineral density quantitative trait locus 8 9.8
626 microvascular complications of diabetes 3 9.8
627 microvascular complications of diabetes 4 9.8
628 microvascular complications of diabetes 6 9.8
629 microvascular complications of diabetes 7 9.8
630 bone mineral density quantitative trait locus 15 9.8
631 alacrima, achalasia, and mental retardation syndrome 9.8
632 severe congenital neutropenia 9.8
633 withdrawal disorder 9.8
634 igg4-related disease 9.8
635 sleeping sickness 9.8
636 osteomyelitis 9.8
637 tonsillitis 9.8
638 rickets 9.8
639 pertussis 9.8
640 microcytic anemia 9.8
641 gestational diabetes 9.8
642 cortical blindness 9.8
643 inflammatory spondylopathy 9.8
644 crimean-congo hemorrhagic fever 9.8
645 dilated cardiomyopathy 9.8
646 carotid stenosis 9.8
647 transient global amnesia 9.8
648 rift valley fever 9.8
649 schistosomiasis 9.8
650 adult-onset still's disease 9.8
651 mixed malaria 9.8
652 neuroleptic malignant syndrome 9.8
653 arthus reaction 9.8
654 rheumatic disease 9.8
655 ventricular septal defect 9.8
656 histoplasmosis 9.8
657 melanoma 9.8
658 leiomyosarcoma 9.8
659 macrocytic anemia 9.8
660 splenic abscess 9.8
661 chorioangioma 9.8
662 idiopathic interstitial pneumonia 9.8
663 interstitial lung disease 9.8
664 chronic granulomatous disease 9.8
665 arthropathy 9.8
666 insulinoma 9.8
667 merkel cell carcinoma 9.8
668 coronary stenosis 9.8
669 milk allergy 9.8
670 hypokalemia 9.8
671 rapidly progressive glomerulonephritis 9.8
672 thyroid gland disease 9.8
673 ovarian cyst 9.8
674 urinary tract obstruction 9.8
675 hemangioblastoma 9.8
676 human immunodeficiency virus infectious disease 9.8
677 intestinal disease 9.8
678 paraplegia 9.8
679 adenoma 9.8
680 spondylitis 9.8
681 monoclonal gammopathy of uncertain significance 9.8
682 cocaine abuse 9.8
683 localized scleroderma 9.8
684 erythema infectiosum 9.8
685 amyloidosis 9.8
686 cholangitis 9.8
687 stomatitis 9.8
688 congenital syphilis 9.8
689 hypoplastic left heart syndrome 9.8
690 periostitis 9.8
691 congenital hepatic fibrosis 9.8
692 sall4-related disorders 9.8
693 sickle cell disease 9.8
694 banti's syndrome 9.8
695 congenital cytomegalovirus 9.8
696 coronary artery aneurysm 9.8
697 encephalocele 9.8
698 giant cell myocarditis 9.8
699 glioma 9.8
700 haemophilus influenzae 9.8
701 lymphocytic hypophysitis 9.8
702 lymphosarcoma 9.8
703 meningococcemia 9.8
704 wandering spleen 9.8
705 raynaud phenomenon 9.8
706 depression 9.8
707 head injury 9.8
708 pituitary tumors 9.8
709 glial tumor 9.8
710 hemolytic disease due to fetomaternal alloimmunization 9.8
711 rare lymphatic malformation 9.8
712 acute radiation syndrome 9.8
713 diffuse alveolar hemorrhage 9.8
714 hepatosplenic t-cell lymphoma 9.8
715 pediatric systemic lupus erythematosus 9.8
716 neurofibromatosis, type ii 9.7
717 amyotrophic lateral sclerosis 1 9.7
718 blue rubber bleb nevus 9.7
719 cardiac arrhythmia 9.7
720 cleft palate, isolated 9.7
721 immunoglobulin a deficiency 1 9.7
722 holt-oram syndrome 9.7
723 hypertension, essential 9.7
724 ige responsiveness, atopic 9.7
725 leukemia, acute monocytic 9.7
726 lipomatosis, multiple 9.7
727 chromosome 5q deletion syndrome 9.7
728 teratoma, ovarian 9.7
729 platelet groups--ko system 9.7
730 strabismus 9.7
731 anemia, hypochromic microcytic, with iron overload 1 9.7
732 eosinophilic fasciitis 9.7
733 factor v deficiency 9.7
734 hydrocephalus, congenital, 1 9.7
735 hypervitaminosis a 9.7
736 3-methylglutaconic aciduria, type iii 9.7
737 schizencephaly 9.7
738 mayer-rokitansky-kuster-hauser syndrome 9.7
739 neutropenia, severe congenital, x-linked 9.7
740 prostatic hyperplasia, benign 9.7
741 adenomyosis 9.7
742 cervical cancer 9.7
743 aceruloplasminemia 9.7
744 progressive familial heart block, type ib 9.7
745 gastrointestinal stromal tumor 9.7
746 endometrial cancer 9.7
747 myocardial infarction 2 9.7
748 fatty liver disease, nonalcoholic 1 9.7
749 von willebrand disease, type 2 9.7
750 membranous nephropathy 9.7
751 melioidosis 9.7
752 cholangiocarcinoma 9.7
753 carbonic anhydrase va deficiency, hyperammonemia due to 9.7
754 chorea, childhood-onset, with psychomotor retardation 9.7
755 spastic paraplegia, intellectual disability, nystagmus, and obesity 9.7
756 mucopolysaccharidosis-plus syndrome 9.7
757 polymicrogyria with or without vascular-type ehlers-danlos syndrome 9.7
758 cryptogenic organizing pneumonia 9.7
759 hypophosphatemia 9.7
760 hyperphosphatemia 9.7
761 variola major 9.7
762 hypochromic microcytic anemia 9.7
763 metabolic acidosis 9.7
764 hemorrhagic cystitis 9.7
765 marantic endocarditis 9.7
766 crohn's colitis 9.7
767 scoliosis 9.7
768 griscelli syndrome 9.7
769 bone disease 9.7
770 bone resorption disease 9.7
771 cryptococcal meningitis 9.7
772 hepatic veno-occlusive disease 9.7
773 mucositis 9.7
774 sitosterolemia 9.7
775 sensorineural hearing loss 9.7
776 cerebral artery occlusion 9.7
777 pleomorphic lipoma 9.7
778 cholelithiasis 9.7
779 pleurisy 9.7
780 common cold 9.7
781 nasopharyngitis 9.7
782 short bowel syndrome 9.7
783 open-angle glaucoma 9.7
784 japanese encephalitis 9.7
785 hydronephrosis 9.7
786 prostatic hypertrophy 9.7
787 t cell deficiency 9.7
788 primary hyperparathyroidism 9.7
789 plethora of newborn 9.7
790 erysipelas 9.7
791 hepatorenal syndrome 9.7
792 clubfoot 9.7
793 vaginal cancer 9.7
794 chagas disease 9.7
795 goiter 9.7
796 hepatic coma 9.7
797 telangiectasis 9.7
798 choreatic disease 9.7
799 relapsing fever 9.7
800 focal segmental glomerulosclerosis 9.7
801 uveitis 9.7
802 gout 9.7
803 right bundle branch block 9.7
804 porphyria 9.7
805 mycoplasma pneumoniae pneumonia 9.7
806 hepatic encephalopathy 9.7
807 hyperparathyroidism 9.7
808 obstructive jaundice 9.7
809 biliary atresia 9.7
810 patent foramen ovale 9.7
811 familial hypercholesterolemia 9.7
812 facial paralysis 9.7
813 alcoholic liver cirrhosis 9.7
814 bipolar i disorder 9.7
815 capillary leak syndrome 9.7
816 neuroendocrine tumor 9.7
817 duodenal ulcer 9.7
818 squamous cell carcinoma 9.7
819 neuroendocrine carcinoma 9.7
820 optic nerve disease 9.7
821 hyperinsulinism 9.7
822 enthesopathy 9.7
823 focal epilepsy 9.7
824 granulomatous hepatitis 9.7
825 lateral sclerosis 9.7
826 colon adenocarcinoma 9.7
827 myelophthisic anemia 9.7
828 protein s deficiency 9.7
829 angiodysplasia 9.7
830 transitional cell carcinoma 9.7
831 acute interstitial pneumonia 9.7
832 acalculous cholecystitis 9.7
833 prostatic adenoma 9.7
834 cervix carcinoma 9.7
835 membranoproliferative glomerulonephritis 9.7
836 severe acute respiratory syndrome 9.7
837 germ cell cancer 9.7
838 testicular cancer 9.7
839 substance abuse 9.7
840 myelitis 9.7
841 fibrosarcoma 9.7
842 carotid artery disease 9.7
843 breast adenocarcinoma 9.7
844 mastocytosis 9.7
845 lactic acidosis 9.7
846 intermittent claudication 9.7
847 plasmacytoma 9.7
848 pulmonary fibrosis 9.7
849 pituitary adenoma 9.7
850 intestinal pseudo-obstruction 9.7
851 acute myocarditis 9.7
852 bladder urothelial carcinoma 9.7
853 pancreatic adenocarcinoma 9.7
854 heart valve disease 9.7
855 intracranial embolism 9.7
856 clear cell renal cell carcinoma 9.7
857 rhinitis 9.7
858 subacute bacterial endocarditis 9.7
859 endophthalmitis 9.7
860 proliferative glomerulonephritis 9.7
861 immune-complex glomerulonephritis 9.7
862 cavernous hemangioma 9.7
863 intrahepatic cholangiocarcinoma 9.7
864 chronic inflammatory demyelinating polyradiculoneuropathy 9.7
865 demyelinating polyneuropathy 9.7
866 schizoaffective disorder 9.7
867 testicular germ cell cancer 9.7
868 ovarian germ cell teratoma 9.7
869 acute pyelonephritis 9.7
870 inferior myocardial infarction 9.7
871 conjunctivitis 9.7
872 t-cell leukemia 9.7
873 situs inversus 9.7
874 neuroblastoma 9.7
875 appendicitis 9.7
876 ileus 9.7
877 monocytic leukemia 9.7
878 herpes zoster 9.7
879 malignant hyperthermia 9.7
880 smallpox 9.7
881 mechanical strabismus 9.7
882 diabetes insipidus 9.7
883 bronchiectasis 9.7
884 fasciitis 9.7
885 aphthous stomatitis 9.7
886 alopecia areata 9.7
887 drug dependence 9.7
888 hypertrophic cardiomyopathy 9.7
889 polymicrogyria 9.7
890 acquired pure red cell aplasia 9.7
891 acute monoblastic leukemia 9.7
892 anca-associated vasculitis 9.7
893 cytomegalic inclusion disease 9.7
894 dwarfism 9.7
895 fetal thalidomide syndrome 9.7
896 hemophagocytic reticulosis 9.7
897 homologous wasting disease 9.7
898 horseshoe kidney 9.7
899 hypoadrenalism 9.7
900 hypoaldosteronism 9.7
901 kaposiform hemangioendothelioma 9.7
902 may-thurner syndrome 9.7
903 neisseria meningitidis infection 9.7
904 non-involuting congenital hemangioma 9.7
905 polymyositis 9.7
906 retroperitoneal fibrosis 9.7
907 brain injury 9.7
908 hypotonia 9.7
909 paraneoplastic syndromes 9.7
910 monosomy 21 9.7
911 systemic autoimmune disease 9.7
912 cerebrofacial arteriovenous metameric syndrome 9.7
913 obsolete: rapidly progressive glomerulonephritis 9.7
914 neonatal alloimmune neutropenia 9.7
915 avascular necrosis 9.7
916 large granular lymphocyte leukemia 9.7
917 rare tumor 9.7
918 overgrowth syndrome 9.7
919 thyroid carcinoma 9.7
920 achondroplasia 9.5
921 aniridia 1 9.5
922 arteriovenous malformations of the brain 9.5
923 gastroesophageal reflux 9.5
924 aortic valve disease 1 9.5
925 burkitt lymphoma 9.5
926 cerebral cavernous malformations 9.5
927 split-hand/foot malformation with long bone deficiency 1 9.5
928 cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 9.5
929 preauricular fistulae, congenital 9.5
930 erythrokeratodermia variabilis et progressiva 1 9.5
931 esophageal cancer 9.5
932 lymphoma, mucosa-associated lymphoid type 9.5
933 glaucoma, primary open angle 9.5
934 glioma susceptibility 1 9.5
935 heinz body anemias 9.5
936 diaphragmatic hernia, congenital 9.5
937 hernia, hiatus 9.5
938 attention deficit-hyperactivity disorder 9.5
939 hypertelorism 9.5
940 inclusion body myositis 9.5
941 meckel diverticulum 9.5
942 neurofibromatosis, type iv, of riccardi 9.5
943 cyclic neutropenia 9.5
944 neutrophilia, hereditary 9.5
945 otitis media 9.5
946 nephrolithiasis, calcium oxalate 9.5
947 papillomatosis, confluent and reticulated 9.5
948 pectus excavatum 9.5
949 pigmented purpuric eruption 9.5
950 proline-negative auxotroph of hamster, complementation of 9.5
951 pulmonary hemosiderosis 9.5
952 dowling-degos disease 1 9.5
953 schizophrenia 9.5
954 sneddon syndrome 9.5
955 odontochondrodysplasia 9.5
956 telecanthus 9.5
957 suppressor of tumorigenicity 3 9.5
958 renal hypodysplasia/aplasia 1 9.5
959 vesicoureteral reflux 1 9.5
960 volvulus of midgut 9.5
961 wilms tumor 1 9.5
962 wolf-hirschhorn syndrome 9.5
963 abetalipoproteinemia 9.5
964 anus, imperforate 9.5
965 ataxia-telangiectasia 9.5
966 sitosterolemia 1 9.5
967 bloom syndrome 9.5
968 congenital disorder of glycosylation, type i/iix 9.5
969 premature centromere division 9.5
970 cerebrotendinous xanthomatosis 9.5
971 cholesterol pneumonia 9.5
972 chondrosarcoma 9.5
973 chordoma 9.5
974 cohen syndrome 9.5
975 complement component 2 deficiency 9.5
976 baller-gerold syndrome 9.5
977 diastrophic dysplasia 9.5
978 duodenal atresia 9.5
979 factor vii deficiency 9.5
980 fanconi anemia, complementation group c 9.5
981 galactorrhea 9.5
982 factor xii deficiency 9.5
983 heart block, congenital 9.5
984 hemochromatosis, type 1 9.5
985 mckusick-kaufman syndrome 9.5
986 hyperlipoproteinemia, type i 9.5
987 ichthyosis, congenital, autosomal recessive 4b 9.5
988 schimke immunoosseous dysplasia 9.5
989 intracranial hypertension, idiopathic 9.5
990 keutel syndrome 9.5
991 microcephaly 1, primary, autosomal recessive 9.5
992 moyamoya disease 1 9.5
993 mucolipidosis ii alpha/beta 9.5
994 mucopolysaccharidosis, type vi 9.5
995 galactosialidosis 9.5
996 nonarteritic anterior ischemic optic neuropathy 9.5
997 osteogenic sarcoma 9.5
998 osteopetrosis, autosomal recessive 1 9.5
999 subacute sclerosing panencephalitis 9.5
1000 abnormal hair, joint laxity, and developmental delay 9.5
1001 pituitary hormone deficiency, combined, 2 9.5
1002 porphyria, congenital erythropoietic 9.5
1003 pseudoxanthoma elasticum 9.5
1004 respiratory distress syndrome in premature infants 9.5
1005 rhabdomyosarcoma 2 9.5
1006 rheumatic fever-related antigen 9.5
1007 sc phocomelia syndrome 9.5
1008 smith-lemli-opitz syndrome 9.5
1009 testicular germ cell tumor 9.5
1010 tibial hemimelia 9.5
1011 opitz gbbb syndrome, type i 9.5
1012 intestinal pseudoobstruction, neuronal, chronic idiopathic, x-linked 9.5
1013 androgen insensitivity syndrome 9.5
1014 body mass index quantitative trait locus 11 9.5
1015 radial ray deficiency, x-linked 9.5
1016 hypophosphatemic rickets, x-linked recessive 9.5
1017 sarcoma, synovial 9.5
1018 dyskeratosis congenita, x-linked 9.5
1019 isolated growth hormone deficiency, type iii, with agammaglobulinemia 9.5
1020 mucopolysaccharidosis, type ii 9.5
1021 reticuloendotheliosis, x-linked 9.5
1022 kearns-sayre syndrome 9.5
1023 pituitary adenoma, prolactin-secreting 9.5
1024 dermatitis herpetiformis, familial 9.5
1025 spastic paraplegia and evans syndrome 9.5
1026 quebec platelet disorder 9.5
1027 body mass index quantitative trait locus 9 9.5
1028 xanthomatosis 9.5
1029 macular degeneration, age-related, 1 9.5
1030 dermatitis, atopic 9.5
1031 homocysteinemia 9.5
1032 body mass index quantitative trait locus 8 9.5
1033 cerebral cavernous malformations 3 9.5
1034 hemophagocytic lymphohistiocytosis, familial, 2 9.5
1035 sickle cell anemia 9.5
1036 microvascular complications of diabetes 1 9.5
1037 reflex sympathetic dystrophy 9.5
1038 orthostatic intolerance 9.5
1039 hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy 9.5
1040 nonaka myopathy 9.5
1041 atrioventricular septal defect 9.5
1042 body mass index quantitative trait locus 1 9.5
1043 aortic aneurysm, familial thoracic 1 9.5
1044 nasopharyngeal carcinoma 9.5
1045 allergic rhinitis 9.5
1046 coronary heart disease 1 9.5
1047 body mass index quantitative trait locus 4 9.5
1048 body mass index quantitative trait locus 10 9.5
1049 juvenile myelomonocytic leukemia 9.5
1050 anxiety 9.5
1051 neutrophilic dermatosis, acute febrile 9.5
1052 kala-azar 1 9.5
1053 body mass index quantitative trait locus 7 9.5
1054 legionnaire disease 9.5
1055 hypertension, diastolic 9.5
1056 choanal atresia, posterior 9.5
1057 mevalonic aciduria 9.5
1058 retinal cone dystrophy 4 9.5
1059 systemic lupus erythematosus 9 9.5
1060 congenital disorder of glycosylation, type in 9.5
1061 ewing sarcoma 9.5
1062 body mass index quantitative trait locus 12 9.5
1063 body mass index quantitative trait locus 14 9.5
1064 microvascular complications of diabetes 2 9.5
1065 microvascular complications of diabetes 5 9.5
1066 premature ovarian failure 7 9.5
1067 antithrombin iii deficiency 9.5
1068 tumor predisposition syndrome 9.5
1069 complement component 4a deficiency 9.5
1070 peripartum cardiomyopathy 9.5
1071 immunodeficiency, common variable, 8, with autoimmunity 9.5
1072 pulmonary hypertension, primary, 2 9.5
1073 body mass index quantitative trait locus 18 9.5
1074 cole disease 9.5
1075 hyperprolactinemia 9.5
1076 analbuminemia 9.5
1077 corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia 9.5
1078 retinitis pigmentosa and erythrocytic microcytosis 9.5
1079 erythrokeratodermia variabilis et progressiva 4 9.5
1080 helix syndrome 9.5
1081 erythrokeratodermia variabilis et progressiva 5 9.5
1082 alkuraya-kucinskas syndrome 9.5
1083 body mass index quantitative trait locus 19 9.5
1084 body mass index quantitative trait locus 20 9.5
1085 west syndrome 9.5
1086 aspirin allergy 9.5
1087 streptococcus pneumonia 9.5
1088 drug-induced lupus erythematosus 9.5
1089 autoimmune vasculitis 9.5
1090 pemphigus gestationis 9.5
1091 human monocytic ehrlichiosis 9.5
1092 invasive aspergillosis 9.5
1093 adenoiditis 9.5
1094 swine influenza 9.5
1095 foodborne botulism 9.5
1096 periventricular nodular heterotopia 9.5
1097 early congenital syphilis 9.5
1098 exanthema subitum 9.5
1099 adult t-cell leukemia 9.5
1100 tooth agenesis 9.5
1101 extrapulmonary tuberculosis 9.5
1102 funisitis 9.5
1103 peripheral t-cell lymphoma 9.5
1104 rheumatic heart disease 9.5
1105 peripheral artery disease 9.5
1106 oculogyric crisis 9.5
1107 sleep apnea 9.5
1108 chronic venous insufficiency 9.5
1109 renal fibrosis 9.5
1110 colorectal adenocarcinoma 9.5
1111 townes-brocks syndrome 9.5
1112 tonsil squamous cell carcinoma 9.5
1113 mucosal melanoma 9.5
1114 interleukin-7 receptor alpha deficiency 9.5
1115 autism spectrum disorder 9.5
1116 cutaneous t cell lymphoma 9.5
1117 apraxia 9.5
1118 ileitis 9.5
1119 agraphia 9.5
1120 dyschromatosis universalis hereditaria 9.5
1121 persistent generalized lymphadenopathy 9.5
1122 lung abscess 9.5
1123 umbilical hernia 9.5
1124 glucocorticoid-induced osteoporosis 9.5
1125 metal allergy 9.5
1126 dextro-looped transposition of the great arteries 9.5
1127 salmonellosis 9.5
1128 miyoshi muscular dystrophy 9.5
1129 myoglobinuria 9.5
1130 cytomegalovirus retinitis 9.5
1131 acquired generalized lipodystrophy 9.5
1132 polycystic kidney disease 9.5
1133 mucolipidosis 9.5
1134 thyroid gland anaplastic carcinoma 9.5
1135 myxofibrosarcoma 9.5
1136 non-alcoholic steatohepatitis 9.5
1137 coronavirus infection 9.5
1138 split hand-foot malformation 9.5
1139 venous insufficiency 9.5
1140 xerophthalmia 9.5
1141 osteonecrosis 9.5
1142 neuroretinitis 9.5
1143 louping ill 9.5
1144 left bundle branch hemiblock 9.5
1145 parotitis 9.5
1146 sialadenitis 9.5
1147 siderosis 9.5
1148 prolymphocytic leukemia 9.5
1149 legionellosis 9.5
1150 esophageal atresia 9.5
1151 viral pneumonia 9.5
1152 microinvasive gastric cancer 9.5
1153 osteomalacia 9.5
1154 leukodystrophy 9.5
1155 tropical sprue 9.5
1156 protein-losing enteropathy 9.5
1157 renal hypertension 9.5
1158 mesenteric lymphadenitis 9.5
1159 intracranial aneurysm 9.5
1160 discitis 9.5
1161 corneal edema 9.5
1162 meconium aspiration syndrome 9.5
1163 placenta praevia 9.5
1164 q fever 9.5
1165 bartonellosis 9.5
1166 henoch-schoenlein purpura 9.5
1167 hypoparathyroidism 9.5
1168 allergic conjunctivitis 9.5
1169 neonatal anemia 9.5
1170 arteriovenous malformation 9.5
1171 mobitz type ii atrioventricular block 9.5
1172 lemierre's syndrome 9.5
1173 phlebotomus fever 9.5
1174 megacolon 9.5
1175 epidural abscess 9.5
1176 xanthogranulomatous pyelonephritis 9.5
1177 listeriosis 9.5
1178 cauda equina syndrome 9.5
1179 patau syndrome 9.5
1180 neonatal diabetes mellitus 9.5
1181 choledocholithiasis 9.5
1182 ecthyma 9.5
1183 esophagitis 9.5
1184 pulmonary alveolar proteinosis 9.5
1185 aseptic meningitis 9.5
1186 oligohydramnios 9.5
1187 alcoholic hepatitis 9.5
1188 bronchopneumonia 9.5
1189 leiomyoma 9.5
1190 newborn respiratory distress syndrome 9.5
1191 quadriplegia 9.5
1192 keratoconjunctivitis sicca 9.5
1193 plasmodium ovale malaria 9.5
1194 hereditary spherocytosis 9.5
1195 leukostasis 9.5
1196 dementia 9.5
1197 branch retinal artery occlusion 9.5
1198 intestinal tuberculosis 9.5
1199 congenital dyserythropoietic anemia 9.5
1200 skin sarcoidosis 9.5
1201 cardiac sarcoidosis 9.5
1202 congenital hypoplastic anemia 9.5
1203 splenic artery aneurysm 9.5
1204 algoneurodystrophy 9.5
1205 autoimmune polyendocrine syndrome 9.5
1206 pulmonary valve insufficiency 9.5
1207 sclerosing cholangitis 9.5
1208 ascending cholangitis 9.5
1209 pyuria 9.5
1210 gonadal dysgenesis 9.5
1211 pemphigoid gestationis 9.5
1212 glossitis 9.5
1213 labyrinthitis 9.5
1214 cholera 9.5
1215 rheumatic fever 9.5
1216 keratosis 9.5
1217 chronic cystitis 9.5
1218 ichthyosis 9.5
1219 retinal vein occlusion 9.5
1220 factitious disorder 9.5
1221 toxic megacolon 9.5
1222 status epilepticus 9.5
1223 epilepsy 9.5
1224 mononeuritis multiplex 9.5
1225 hyperuricemia 9.5
1226 bardet-biedl syndrome 9.5
1227 encephalomalacia 9.5
1228 constipation 9.5
1229 b cell deficiency 9.5
1230 ectodermal dysplasia 9.5
1231 ascending colon cancer 9.5
1232 factor xiii deficiency 9.5
1233 nocardiosis 9.5
1234 arteriosclerosis 9.5
1235 retinal vascular disease 9.5
1236 sensory peripheral neuropathy 9.5
1237 transverse colon cancer 9.5
1238 kidney cancer 9.5
1239 cystic teratoma 9.5
1240 adenofibroma 9.5
1241 acrodermatitis 9.5
1242 epidermolysis bullosa 9.5
1243 contact dermatitis 9.5
1244 rectosigmoid cancer 9.5
1245 bronchiolitis obliterans 9.5
1246 middle lobe syndrome 9.5
1247 long qt syndrome 9.5
1248 endometrial adenocarcinoma 9.5
1249 immune system disease 9.5
1250 hypersensitivity reaction type iv disease 9.5
1251 newcastle disease 9.5
1252 bronchiolitis 9.5
1253 cockayne syndrome 9.5
1254 lobular neoplasia 9.5
1255 allergic contact dermatitis 9.5
1256 food allergy 9.5
1257 churg-strauss syndrome 9.5
1258 astrocytoma 9.5
1259 malignant glioma 9.5
1260 cystic lymphangioma 9.5
1261 gingivitis 9.5
1262 lipomatosis 9.5
1263 oligodendroglioma 9.5
1264 lysosomal storage disease 9.5
1265 pleomorphic rhabdomyosarcoma 9.5
1266 inappropriate adh syndrome 9.5
1267 carotid artery thrombosis 9.5
1268 mammary paget's disease 9.5
1269 turner syndrome 9.5
1270 signet ring cell adenocarcinoma 9.5
1271 retinitis 9.5
1272 gastric adenocarcinoma 9.5
1273 hermansky-pudlak syndrome 9.5
1274 pleural empyema 9.5
1275 porokeratosis 9.5
1276 shwartzman phenomenon 9.5
1277 craniopharyngioma 9.5
1278 colonic pseudo-obstruction 9.5
1279 bartholin's gland carcinoma 9.5
1280 multidrug-resistant tuberculosis 9.5
1281 tricuspid valve insufficiency 9.5
1282 agnosia 9.5
1283 primary syphilis 9.5
1284 rh isoimmunization 9.5
1285 hyperglycemia 9.5
1286 histiocytoma 9.5
1287 polyradiculopathy 9.5
1288 epidermolysis bullosa acquisita 9.5
1289 erdheim-chester disease 9.5
1290 myofibroma 9.5
1291 cutaneous fibrous histiocytoma 9.5
1292 juvenile xanthogranuloma 9.5
1293 dysgerminoma 9.5
1294 macular retinal edema 9.5
1295 breast angiosarcoma 9.5
1296 dysgraphia 9.5
1297 intestinal benign neoplasm 9.5
1298 gastric neuroendocrine neoplasm 9.5
1299 extragonadal germ cell cancer 9.5
1300 brain edema 9.5
1301 calciphylaxis 9.5
1302 placenta accreta 9.5
1303 anti-basement membrane glomerulonephritis 9.5
1304 benign ependymoma 9.5
1305 pilocytic astrocytoma of cerebellum 9.5
1306 colorado tick fever 9.5
1307 lymph node tuberculosis 9.5
1308 tubular adenocarcinoma 9.5
1309 pericardial tuberculosis 9.5
1310 myelodysplastic/myeloproliferative neoplasm 9.5
1311 alcoholic pancreatitis 9.5
1312 ovarian cystic teratoma 9.5
1313 gastric leiomyosarcoma 9.5
1314 blepharospasm 9.5
1315 anterograde amnesia 9.5
1316 hemoglobin d disease 9.5
1317 paget's disease of bone 9.5
1318 dystonia 9.5
1319 cellular ependymoma 9.5
1320 mature teratoma 9.5
1321 chiasmal syndrome 9.5
1322 pleomorphic carcinoma 9.5
1323 adrenal neuroblastoma 9.5
1324 adenosine deaminase deficiency 9.5
1325 apical myocardial infarction 9.5
1326 subendocardial myocardial infarction 9.5
1327 posterolateral myocardial infarction 9.5
1328 lateral myocardial infarction 9.5
1329 silent myocardial infarction 9.5
1330 anteroseptal myocardial infarction 9.5
1331 eosinophilic pneumonia 9.5
1332 mitral valve disease 9.5
1333 bronchitis 9.5
1334 reactive arthritis 9.5
1335 thyroid hyalinizing trabecular adenoma 9.5
1336 inflammatory breast carcinoma 9.5
1337 corpus callosum lipoma 9.5
1338 acute disseminated encephalomyelitis 9.5
1339 double outlet right ventricle 9.5
1340 pulmonary valve stenosis 9.5
1341 juvenile pilocytic astrocytoma 9.5
1342 skin tag 9.5
1343 mature b-cell neoplasm 9.5
1344 sarcomatosis 9.5
1345 macular holes 9.5
1346 muscular atrophy 9.5
1347 gastrointestinal system disease 9.5
1348 delusional disorder 9.5
1349 placenta disease 9.5
1350 hemarthrosis 9.5
1351 carotid artery occlusion 9.5
1352 septic arthritis 9.5
1353 periodontitis 9.5
1354 intestinal obstruction 9.5
1355 retinal artery occlusion 9.5
1356 mucormycosis 9.5
1357 polyhydramnios 9.5
1358 dermatitis herpetiformis 9.5
1359 chronic fatigue syndrome 9.5
1360 genital herpes 9.5
1361 in situ carcinoma 9.5
1362 bacterial pneumonia 9.5
1363 dermatophytosis 9.5
1364 atrophic gastritis 9.5
1365 sideroblastic anemia 9.5
1366 autosomal dominant polycystic kidney disease 9.5
1367 hepatopulmonary syndrome 9.5
1368 pityriasis versicolor 9.5
1369 leishmaniasis 9.5
1370 cutaneous leishmaniasis 9.5
1371 gas gangrene 9.5
1372 pemphigus 9.5
1373 diabetic macular edema 9.5
1374 erythromelalgia 9.5
1375 homocystinuria 9.5
1376 priapism 9.5
1377 lymphangitis 9.5
1378 status asthmaticus 9.5
1379 exophthalmos 9.5
1380 hypopituitarism 9.5
1381 hypertensive encephalopathy 9.5
1382 intracranial hypertension 9.5
1383 lipid storage disease 9.5
1384 senile cataract 9.5
1385 pulmonary emphysema 9.5
1386 biliary tract disease 9.5
1387 omsk hemorrhagic fever 9.5
1388 baraitser-winter cerebrofrontofacial syndrome 9.5
1389 congenital disorders of n-linked glycosylation and multiple pathway 9.5
1390 acute leukemia of ambiguous lineage 9.5
1391 aminoaciduria 9.5
1392 angioimmunoblastic lymphadenopathy with dysproteinemia 9.5
1393 angiosarcoma of the scalp 9.5
1394 asherman's syndrome 9.5
1395 autoimmune myocarditis 9.5
1396 bone marrow necrosis 9.5
1397 broken heart syndrome 9.5
1398 bronchopulmonary dysplasia 9.5
1399 chromosome 4p deletion 9.5
1400 congenital human immunodeficiency virus 9.5
1401 congenital mumps 9.5
1402 cutaneous sclerosis 9.5
1403 dextrocardia with situs inversus 9.5
1404 diffuse neonatal hemangiomatosis 9.5
1405 eisenmenger syndrome 9.5
1406 exfoliative dermatitis 9.5
1407 fasting hypoglycemia 9.5
1408 fournier gangrene 9.5
1409 gianotti crosti syndrome 9.5
1410 glucagonoma 9.5
1411 growth hormone deficiency 9.5
1412 idiopathic neutropenia 9.5
1413 lathyrism 9.5
1414 laugier-hunziker syndrome 9.5
1415 lymphoma aids related 9.5
1416 macrophage activation syndrome 9.5
1417 meningococcal infection 9.5
1418 meningoencephalocele 9.5
1419 mercury poisoning 9.5
1420 mollaret meningitis 9.5
1421 myelodysplastic syndrome with excess blasts 9.5
1422 myelodysplastic syndrome with single lineage dysplasia 9.5
1423 nephrogenic systemic fibrosis 9.5
1424 nonseminomatous germ cell tumor 9.5
1425 orbital lymphangioma 9.5
1426 paroxysmal cold hemoglobinuria 9.5
1427 pemphigus foliaceus 9.5
1428 plasmablastic lymphoma 9.5
1429 pure autonomic failure 9.5
1430 pustular psoriasis 9.5
1431 ring chromosome 21 9.5
1432 rosai-dorfman disease 9.5
1433 scleromyxedema 9.5
1434 shapiro syndrome 9.5
1435 sickle beta thalassemia 9.5
1436 single ventricular heart 9.5
1437 stevens-johnson syndrome/toxic epidermal necrolysis 9.5
1438 superficial siderosis of the central nervous system 9.5
1439 transverse myelitis 9.5
1440 triploidy 9.5
1441 tuberculous meningitis 9.5
1442 undifferentiated connective tissue disease 9.5
1443 virus associated hemophagocytic syndrome 9.5
1444 cryptogenic cirrhosis 9.5
1445 isolated pierre robin sequence 9.5
1446 autonomic dysfunction 9.5
1447 cavernous malformation 9.5
1448 cerebral atrophy 9.5
1449 myoclonus 9.5
1450 paresthesia 9.5
1451 spasticity 9.5
1452 immuno-osseous dysplasia 9.5
1453 mixed germ cell tumor 9.5
1454 obsolete: heinz body anemia 9.5
1455 b-cell non-hodgkin lymphoma 9.5
1456 t-cell non-hodgkin lymphoma 9.5
1457 differentiated thyroid carcinoma 9.5
1458 endotheliitis 9.5
1459 epithelioid hemangioendothelioma 9.5
1460 hemimelia 9.5
1461 hemophagocytic syndrome associated with an infection 9.5
1462 secondary hemophagocytic lymphohistiocytosis 9.5
1463 rare hemorrhagic disorder 9.5
1464 superficial siderosis 9.5
1465 autosomal recessive malignant osteopetrosis 9.5
1466 occipital encephalocele 9.5
1467 pulmonary arterial hypertension associated with portal hypertension 9.5
1468 autoimmune polyendocrinopathy type 4 9.5
1469 virus-associated trichodysplasia spinulosa 9.5
1470 acute pandysautonomia 9.5
1471 bilateral massive adrenal hemorrhage 9.5
1472 ring chromosome 9.5
1473 fixed drug eruption 9.5
1474 epstein-barr virus-associated malignant lymphoproliferative disorder 9.5
1475 neonatal lupus erythematosus 9.5
1476 neonatal dermatomyositis 9.5
1477 secondary sclerosing cholangitis 9.5
1478 acquired prothrombin deficiency 9.5
1479 longitudinal limb defect 9.5
1480 digitalis poisoning 9.5
1481 congenital amyoplasia 9.5
1482 benign idiopathic neonatal seizures 9.5
1483 recurrent acute pancreatitis 9.5
1484 classic hairy cell leukemia 9.5
1485 rare chromosomal anomaly 9.5
1486 moderate and severe traumatic brain injury 9.5
1487 mixed-type autoimmune hemolytic anemia 9.5
1488 autoimmune hemolytic anemia, warm type 9.5
1489 lymphedema 9.5
1490 erythrokeratoderma 9.5
1491 x-linked intellectual disability-macrocephaly-macroorchidism syndrome 9.5
1492 primary hypophysitis 9.5
1493 light and heavy chain deposition disease 9.5
1494 heavy chain deposition disease 9.5
1495 rare coagulation disorder 9.5
1496 rickettsial disease 9.5
1497 aregenerative anemia 9.5
1498 streptococcal toxic-shock syndrome 9.5
1499 acute megakaryoblastic leukemia in down syndrome 9.5

Graphical network of the top 20 diseases related to Thrombocytopenia:



Diseases related to Thrombocytopenia

Symptoms & Phenotypes for Thrombocytopenia

GenomeRNAi Phenotypes related to Thrombocytopenia according to GeneCards Suite gene sharing:

26 (showing 1, show less)
# Description GenomeRNAi Source Accession Score Top Affiliating Genes
1 Reduced mammosphere formation GR00396-S 9.17 ETV6 GATA1 GP1BA ITGA2 ITGA2B RBM8A

MGI Mouse Phenotypes related to Thrombocytopenia:

45 (showing 5, show less)
# Description MGI Source Accession Score Top Affiliating Genes
1 cellular MP:0005384 10.17 CYCS ETV6 GATA1 GP1BA HOXA11 ITGA2
2 hematopoietic system MP:0005397 10 ADAMTS13 CYCS ETV6 GATA1 GP1BA GP1BB
3 embryo MP:0005380 9.91 CYCS ETV6 GATA1 ITGA2B ITGB3 MASTL
4 homeostasis/metabolism MP:0005376 9.77 ADAMTS13 ANKRD26 ETV6 GATA1 GP1BA GP1BB
5 immune system MP:0005387 9.36 ADAMTS13 CYCS ETV6 GATA1 GP1BB ITGA2B

Drugs & Therapeutics for Thrombocytopenia

PubMed Health treatment related to Thrombocytopenia: 62

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 544, 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
Sodium citrate Approved, Investigational Phase 4 68-04-2
4
Hydroxychloroquine Approved Phase 4 118-42-3 3652
5
Atorvastatin Approved Phase 4 134523-00-5 60823
6
Hydrocortisone acetate Approved, Vet_approved Phase 4 50-03-3
7
Hydrocortisone Approved, Vet_approved Phase 4 50-23-7 5754
8
Peginterferon alfa-2b Approved Phase 4 215647-85-1, 99210-65-8
9
Estradiol Approved, Investigational, Vet_approved Phase 4 50-28-2 5757
10
Polyestradiol phosphate Approved Phase 4 28014-46-2
11
Ethinyl Estradiol Approved Phase 4 57-63-6 5991
12
Bupivacaine Approved, Investigational Phase 4 38396-39-3, 2180-92-9 2474
13
Acetaminophen Approved Phase 4 103-90-2 1983
14
Abciximab Approved Phase 4 143653-53-6
15
Phylloquinone Approved, Investigational Phase 4 84-80-0
16
Cefpirome Approved Phase 4 84957-29-9 5479539
17
Norgestimate Approved, Investigational Phase 4 35189-28-7 6540478
18
Moxifloxacin Approved, Investigational Phase 4 151096-09-2, 354812-41-2 152946
19
Tirofiban Approved Phase 4 144494-65-5 60947
20 Bemiparin Approved, Investigational Phase 4 91449-79-5
21
Acenocoumarol Approved, Investigational Phase 4 152-72-7 9052 54676537
22
Ketorolac Approved Phase 4 74103-06-3, 66635-83-4 3826
23
Diphenhydramine Approved, Investigational Phase 4 147-24-0, 58-73-1 3100
24
Promethazine Approved, Investigational Phase 4 60-87-7 4927
25
Pancrelipase Approved, Investigational Phase 4