Thrombocytopenia
Symptom Information:
Symptom ID: | HPO:0001873 | |||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormality of thrombocytes(HPO:0001872) Abnormal platelet count(HPO:0011873) Thrombocytopenia(HPO:0001873) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Abnormality of thrombocytes(HPO:0001872) Thrombocytopenia(HPO:0001873) |
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Database Frequency: | 224 / 7739 | |||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
16q24.3 microdeletion syndrome | (Orphanet:261250) |
22q11.2 deletion syndrome | (Orphanet:567) |
3-methylglutaconic aciduria type 4 | (Orphanet:67048) |
3-phosphoglycerate dehydrogenase deficiency | (Orphanet:79351) |
AICARDI-GOUTIERES SYNDROME 1 | (OMIM:225750) |
AICARDI-GOUTIERES SYNDROME 3 | (OMIM:610329) |
AICARDI-GOUTIERES SYNDROME 4 | (OMIM:610333) |
AICARDI-GOUTIERES SYNDROME 7 | (OMIM:615846) |
Action myoclonus - renal failure syndrome | (Orphanet:163696) |
Acyl-CoA dehydrogenase 9 deficiency | (Orphanet:99901) |
Adams-Oliver syndrome | (Orphanet:974) |
Alpha-thalassemia - myelodysplastic syndrome | (Orphanet:231401) |
Alport syndrome | (Orphanet:63) |
Atypical Gaucher disease due to saposin C deficiency | (Orphanet:309252) |
Atypical hemolytic uremic syndrome | (Orphanet:2134) |
Atypical hemolytic uremic syndrome with B factor anomaly | (Orphanet:93578) |
Atypical hemolytic uremic syndrome with C3 anomaly | (Orphanet:93575) |
Atypical hemolytic uremic syndrome with DGKE deficiency | (Orphanet:357008) |
Atypical hemolytic uremic syndrome with H factor anomaly | (Orphanet:93579) |
Atypical hemolytic uremic syndrome with I factor anomaly | (Orphanet:93580) |
Atypical hemolytic uremic syndrome with MCP/CD46 anomaly | (Orphanet:93576) |
Atypical hemolytic uremic syndrome with anti-factor H antibodies | (Orphanet:93581) |
Atypical hemolytic uremic syndrome with thrombomodulin anomaly | (Orphanet:217023) |
Autosomal recessive lymphoproliferative disease | (Orphanet:238505) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Autosomal thrombocytopenia with normal platelets | (Orphanet:168629) |
BERNARD-SOULIER SYNDROME | (OMIM:231200) |
BLEEDING DISORDER, PLATELET-TYPE, 15 | (OMIM:615193) |
BLEEDING DISORDER, PLATELET-TYPE, 17 | (OMIM:187900) |
BONE MARROW FAILURE SYNDROME 2 | (OMIM:615715) |
Babesiosis | (Orphanet:108) |
Beemer-Ertbruggen syndrome | (Orphanet:1237) |
Beta-thalassemia | (Orphanet:848) |
Beta-thalassemia - X-linked thrombocytopenia | (Orphanet:231393) |
Bilateral striopallidodentate calcinosis | (Orphanet:1980) |
Blackfan-Diamond anemia | (Orphanet:124) |
Bleeding diathesis due to a collagen receptor defect | (Orphanet:73271) |
Blue rubber bleb nevus | (Orphanet:1059) |
CREST syndrome | (Orphanet:90290) |
Castleman disease | (Orphanet:160) |
Central nervous system calcification - deafness - tubular acidosis - anemia | (Orphanet:3240) |
Cernunnos-XLF deficiency | (Orphanet:169079) |
Chédiak-Higashi syndrome | (Orphanet:167) |
Coats plus syndrome | (Orphanet:313838) |
Combined immunodeficiency due to CRAC channel dysfunction | (Orphanet:169090) |
Combined immunodeficiency due to STIM1 deficiency | (Orphanet:317430) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Common variable immunodeficiency | (Orphanet:1572) |
Congenital amegakaryocytic thrombocytopenia | (Orphanet:3319) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Congenital erythropoietic porphyria | (Orphanet:79277) |
Congenital intrauterine infection-like syndrome | (Orphanet:1229) |
Congenital rubella syndrome | (Orphanet:290) |
Congenital short bowel syndrome | (Orphanet:2301) |
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency | (Orphanet:93583) |
Congenital toxoplasmosis | (Orphanet:858) |
Constitutional megaloblastic anemia with severe neurologic disease | (Orphanet:319651) |
Cornelia de Lange syndrome | (Orphanet:199) |
Crimean-Congo hemorrhagic fever | (Orphanet:99827) |
Cyclic neutropenia | (Orphanet:2686) |
DIAMOND-BLACKFAN ANEMIA 1 | (OMIM:105650) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 | (OMIM:127550) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 | (OMIM:613989) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 | (OMIM:613990) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 | (OMIM:224230) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2 | (OMIM:613987) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
Dengue fever | (Orphanet:99828) |
Diabetic embryopathy | (Orphanet:1926) |
Diffuse neonatal hemangiomatosis | (Orphanet:2123) |
Dubowitz syndrome | (Orphanet:235) |
Dyskeratosis congenita | (Orphanet:1775) |
ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNELDEFICIENCY | (OMIM:614520) |
EPSTEIN SYNDROME | (OMIM:153650) |
Early-onset familial noncirrhotic portal hypertension | (ORPHA:494348) |
Ebola hemorrhagic fever | (Orphanet:319218) |
FANCONI ANEMIA, COMPLEMENTATION GROUP A | (OMIM:227650) |
FANCONI ANEMIA, COMPLEMENTATION GROUP C | (OMIM:227645) |
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 | (OMIM:227646) |
FANCONI ANEMIA, COMPLEMENTATION GROUP E | (OMIM:600901) |
FANCONI ANEMIA, COMPLEMENTATION GROUP G | (OMIM:614082) |
FECHTNER SYNDROME | (OMIM:153640) |
FORSYTHE-WAKELING SYNDROME | (OMIM:613606) |
Familial hemophagocytic lymphohistiocytosis | (Orphanet:540) |
Familial platelet syndrome with predisposition to acute myelogenous leukemia | (Orphanet:71290) |
Fanconi anemia | (Orphanet:84) |
Felty syndrome | (Orphanet:47612) |
Fetal Gaucher disease | (Orphanet:85212) |
Fetal parvovirus syndrome | (Orphanet:295) |
GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA | (OMIM:137560) |
Gamma heavy-chain disease | (Orphanet:100026) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Ghosal hematodiaphyseal dysplasia | (Orphanet:1802) |
Good syndrome | (Orphanet:169105) |
Gray platelet syndrome | (Orphanet:721) |
Griscelli disease | (Orphanet:381) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 | (OMIM:267700) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4 | (OMIM:603552) |
HERMANSKY-PUDLAK SYNDROME 5 | (OMIM:614074) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Hereditary folate malabsorption | (Orphanet:90045) |
Hermansky-Pudlak syndrome with neutropenia | (Orphanet:183678) |
Holocarboxylase synthetase deficiency | (Orphanet:79242) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY | (OMIM:614700) |
INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED | (OMIM:300048) |
IVIC syndrome | (Orphanet:2307) |
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | (Orphanet:37042) |
Immune thrombocytopenic purpura | (Orphanet:3002) |
Immunoglobulin-mediated membranoproliferative glomerulonephritis | (Orphanet:329903) |
Isolated agammaglobulinemia | (Orphanet:229717) |
Isovaleric acidemia | (Orphanet:33) |
Jacobsen syndrome | (Orphanet:2308) |
Kasabach-Merritt syndrome | (Orphanet:2330) |
LYMPHOPROLIFERATIVE SYNDROME 1 | (OMIM:613011) |
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1 | (OMIM:308240) |
Lassa fever | (Orphanet:99824) |
Lathosterolosis | (Orphanet:46059) |
Letterer-Siwe disease | (Orphanet:99870) |
Lyell syndrome | (Orphanet:537) |
Lysinuric protein intolerance | (Orphanet:470) |
MAY-HEGGLIN ANOMALY | (OMIM:155100) |
MONOSOMY 7 OF BONE MARROW | (OMIM:252270) |
MYH9-related thrombocytopenia | (Orphanet:182050) |
Marburg hemorrhagic fever | (Orphanet:99826) |
Methylmalonic acidemia with homocystinuria | (Orphanet:26) |
Methylmalonic acidemia with homocystinuria, type cblC | (Orphanet:79282) |
Methylmalonic acidemia with homocystinuria, type cblF | (Orphanet:79284) |
Methylmalonic acidemia with homocystinuria, type cblJ | (Orphanet:369955) |
Mevalonic aciduria | (Orphanet:29) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Myopathy, lactic acidosis, and sideroblastic anemia 2; MLASA2 | (OMIM:613561) |
NOONAN SYNDROME 1 | (OMIM:163950) |
Neonatal hemochromatosis | (Orphanet:446) |
Nijmegen breakage syndrome | (Orphanet:647) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
OSTEOCHONDRODYSPLASIA, RHIZOMELIC, WITH CALLOSAL AGENESIS, THROMBOCYTOPENIA,HYDROCEPHALUS, AND HYPERTENSION | (OMIM:166990) |
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2 | (OMIM:259710) |
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8 | (OMIM:615085) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Omenn syndrome | (Orphanet:39041) |
Osteogenesis imperfecta | (Orphanet:666) |
Osteopetrosis | (Orphanet:2781) |
Osteopetrosis with renal tubular acidosis | (Orphanet:2785) |
PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE | (OMIM:167850) |
PELGER-HUET ANOMALY | (OMIM:169400) |
PLATELET DISORDER, UNDEFINED | (OMIM:173420) |
PLATELET GLYCOPROTEIN IV DEFICIENCY | (OMIM:608404) |
PLATELET SIGNAL PROCESSING DEFECT | (OMIM:173590) |
PREECLAMPSIA/ECLAMPSIA 1 | (OMIM:189800) |
Paris-Trousseau thrombocytopenia | (Orphanet:851) |
Pearson syndrome | (Orphanet:699) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Polycythemia vera | (Orphanet:729) |
Preeclampsia | (Orphanet:275555) |
Primary hypereosinophilic syndrome | (Orphanet:314950) |
Prolidase deficiency | (Orphanet:742) |
Propionic acidemia | (Orphanet:35) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
Quebec platelet disorder | (Orphanet:220436) |
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia | (Orphanet:71289) |
Recurrent infections-myelofibrosis-nephromegaly syndrome | (Orphanet:369852) |
Reticular dysgenesis | (Orphanet:33355) |
Retinopathy - anemia- central nervous system anomalies | (Orphanet:3088) |
Rhabdoid tumor | (Orphanet:69077) |
Roberts syndrome | (Orphanet:3103) |
SEBASTIAN SYNDROME | (OMIM:605249) |
SLC35A1-CDG | (Orphanet:238459) |
STT3B-CDG | (Orphanet:370924) |
SYSTEMIC LUPUS ERYTHEMATOSUS | (OMIM:152700) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Sea-blue histiocytosis | (Orphanet:158029) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Shwachman-Diamond syndrome | (Orphanet:811) |
Stevens-Johnson syndrome | (Orphanet:36426) |
Stormorken-Sjaastad-Langslet syndrome | (Orphanet:3204) |
Sweet syndrome | (Orphanet:3243) |
Systemic mastocytosis | (Orphanet:2467) |
THROMBOCYTOPENIA 3 | (OMIM:273900) |
THROMBOCYTOPENIA 4 | (OMIM:612004) |
THROMBOCYTOPENIA 5 | (OMIM:616216) |
THROMBOCYTOPENIA WITH ELEVATED SERUM IgA AND RENAL DISEASE | (OMIM:314000) |
THROMBOCYTOPENIA, CYCLIC | (OMIM:188020) |
TMEM165-CDG | (Orphanet:314667) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |
Thrombocytopenia - Robin sequence | (Orphanet:3323) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Thrombocytopenia with congenital dyserythropoietic anemia | (Orphanet:67044) |
Thrombotic thrombocytopenic purpura | (Orphanet:54057) |
Thyrocerebrorenal syndrome | (Orphanet:3327) |
Transaldolase deficiency | (Orphanet:101028) |
Transcobalamin deficiency | (Orphanet:859) |
Typical hemolytic uremic syndrome | (Orphanet:90038) |
Tyrosinemia type 1 | (Orphanet:882) |
Viral hemorrhagic fever | (Orphanet:341) |
Vitamin B12-responsive methylmalonic acidemia | (Orphanet:28) |
Vitamin B12-responsive methylmalonic acidemia type cblA | (Orphanet:79310) |
Vitamin B12-responsive methylmalonic acidemia type cblB | (Orphanet:79311) |
Vitamin B12-unresponsive methylmalonic acidemia | (Orphanet:27) |
Vitamin B12-unresponsive methylmalonic acidemia type mut- | (Orphanet:79312) |
Vitamin B12-unresponsive methylmalonic acidemia type mut0 | (Orphanet:289916) |
Von Voss-Cherstvoy syndrome | (Orphanet:3439) |
Von Willebrand disease type 3 | (Orphanet:166096) |
WISKOTT-ALDRICH SYNDROME | (OMIM:277970) |
WISKOTT-ALDRICH SYNDROME | (OMIM:301000) |
WISKOTT-ALDRICH SYNDROME 2 | (OMIM:614493) |
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM | (OMIM:600903) |
WT limb-blood syndrome | (Orphanet:3466) |
Wiskott-Aldrich syndrome | (Orphanet:906) |
Wolfram syndrome 1 | (OMIM:222300) |
Wolfram syndrome, mitochondrial form | (OMIM:598500) |
X-linked Alport syndrome | (Orphanet:88917) |
X-linked agammaglobulinemia | (Orphanet:47) |
X-linked dyserythropoetic anemia with abnormal platelets and neutropenia | (Orphanet:363727) |
X-linked hyper-IgM syndrome | (Orphanet:101088) |
[DEL] NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4 | (OMIM:612541) |
[DEL] SENGERS SYNDROME | (OMIM:212350) |