Acute leukemia
Symptom Information:
Symptom ID: | HPO:0002488 | |||||||||||||||||||||||||||
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 leukocytes(HPO:0001881) Leukemia(HPO:0001909) Acute leukemia(HPO:0002488) Hematological neoplasm(HPO:0004377) Leukemia(HPO:0001909) Acute leukemia(HPO:0002488) Abnormality of the immune system(HPO:0002715) Abnormality of cellular immune system(HPO:0010987) Abnormality of leukocytes(HPO:0001881) Leukemia(HPO:0001909) Acute leukemia(HPO:0002488) Neoplasm(HPO:0002664) Neoplasm by anatomical site(HPO:0011793) Hematological neoplasm(HPO:0004377) Leukemia(HPO:0001909) Acute leukemia(HPO:0002488) MedDRA: Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104) Leukemia(HPO:0001909) Leukaemias acute NEC(MedDRA:10024292) Acute leukemia(HPO:0002488) |
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Database Frequency: | 29 / 7739 | |||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Aggressive systemic mastocytosis | (Orphanet:98850) |
Alpha-thalassemia - myelodysplastic syndrome | (Orphanet:231401) |
Ataxia - pancytopenia | (Orphanet:2585) |
Blackfan-Diamond anemia | (Orphanet:124) |
Bloom syndrome | (Orphanet:125) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
Down syndrome | (Orphanet:870) |
Ellis Van Creveld syndrome | (Orphanet:289) |
Essential thrombocythemia | (Orphanet:3318) |
Familial thrombocytosis | (Orphanet:71493) |
Hashimoto-Pritzker syndrome | (Orphanet:99872) |
LEUKEMIA, ACUTE, ?X-LINKED | (OMIM:308960) |
LI-FRAUMENI SYNDROME 1 | (OMIM:151623) |
LIG4 syndrome | (Orphanet:99812) |
Li-Fraumeni syndrome | (Orphanet:524) |
Mastocytosis | (Orphanet:98292) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
N syndrome | (Orphanet:2608) |
Nasu-Hakola disease | (Orphanet:2770) |
Nijmegen breakage syndrome | (Orphanet:647) |
Noonan syndrome | (Orphanet:648) |
Platelet storage pool disease | (Orphanet:98454) |
Poland syndrome | (Orphanet:2911) |
Polycythemia vera | (Orphanet:729) |
Shwachman-Diamond syndrome | (Orphanet:811) |
Syndromic X-linked ichthyosis | (Orphanet:281090) |
Systemic mastocytosis | (Orphanet:2467) |
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease | (Orphanet:98849) |
Zunich-Kaye syndrome | (Orphanet:3474) |