Leukopenia
Symptom Information:
Symptom ID: | HPO:0001882 | |||||||||||
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 the immune system(HPO:0002715) Abnormality of cellular immune system(HPO:0010987) Abnormality of leukocytes(HPO:0001881) Abnormal leukocyte count(HPO:0011893) Leukopenia(HPO:0001882) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormality of leukocytes(HPO:0001881) Abnormal leukocyte count(HPO:0011893) Leukopenia(HPO:0001882) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Abnormality of leukocytes(HPO:0001881) Leukopenias NEC(MedDRA:10024385) Leukopenia(HPO:0001882) |
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Database Frequency: | 51 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Acute interstitial pneumonia | (Orphanet:79126) |
Adams-Oliver syndrome | (Orphanet:974) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
BONE MARROW FAILURE SYNDROME 2 | (OMIM:615715) |
Babesiosis | (Orphanet:108) |
Camurati-Engelmann disease | (Orphanet:1328) |
Chédiak-Higashi syndrome | (Orphanet:167) |
Cohen syndrome | (Orphanet:193) |
Common variable immunodeficiency | (Orphanet:1572) |
Crimean-Congo hemorrhagic fever | (Orphanet:99827) |
DIAMOND-BLACKFAN ANEMIA 5 | (OMIM:612528) |
DK1-CDG | (Orphanet:91131) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 | (OMIM:613989) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 | (OMIM:613990) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 5 | (OMIM:615190) |
Dengue fever | (Orphanet:99828) |
Ebola hemorrhagic fever | (Orphanet:319218) |
Familial hemophagocytic lymphohistiocytosis | (Orphanet:540) |
Fanconi anemia | (Orphanet:84) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Ghosal hematodiaphyseal dysplasia | (Orphanet:1802) |
Griscelli disease | (Orphanet:381) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 | (OMIM:267700) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
Hereditary folate malabsorption | (Orphanet:90045) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
Isovaleric acidemia | (Orphanet:33) |
Lassa fever | (Orphanet:99824) |
Leprechaunism | (Orphanet:508) |
Lysinuric protein intolerance | (Orphanet:470) |
MYELOLYMPHATIC INSUFFICIENCY | (OMIM:310350) |
Marburg hemorrhagic fever | (Orphanet:99826) |
Mixed connective tissue disease | (Orphanet:809) |
Osteopetrosis | (Orphanet:2781) |
PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE | (OMIM:167850) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Recurrent infections-myelofibrosis-nephromegaly syndrome | (Orphanet:369852) |
Reticular dysgenesis | (Orphanet:33355) |
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET | (OMIM:615934) |
SYSTEMIC LUPUS ERYTHEMATOSUS | (OMIM:152700) |
Systemic mastocytosis | (Orphanet:2467) |
Tyrosinemia type 1 | (Orphanet:882) |
Viral hemorrhagic fever | (Orphanet:341) |
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) |