Myelodysplasia
Symptom Information:
Symptom ID: | HPO:0002863 | |||||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Neoplasm(HPO:0002664) Neoplasm by anatomical site(HPO:0011793) Hematological neoplasm(HPO:0004377) Myelodysplasia(HPO:0002863) Abnormality of blood and blood-forming tissues(HPO:0001871) Hematological neoplasm(HPO:0004377) Myelodysplasia(HPO:0002863) MedDRA: Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104) Leukemia(HPO:0001909) Myelodysplasia(HPO:0002863) |
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Database Frequency: | 30 / 7739 | |||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Alpha-thalassemia | (Orphanet:846) |
Alpha-thalassemia - myelodysplastic syndrome | (Orphanet:231401) |
Autosomal dominant aplasia and myelodysplasia | (Orphanet:314399) |
Blackfan-Diamond anemia | (Orphanet:124) |
DIAMOND-BLACKFAN ANEMIA 1 | (OMIM:105650) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 | (OMIM:127550) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
Dyskeratosis congenita | (Orphanet:1775) |
Essential thrombocythemia | (Orphanet:3318) |
FANCONI ANEMIA, COMPLEMENTATION GROUP G | (OMIM:614082) |
Familial platelet syndrome with predisposition to acute myelogenous leukemia | (Orphanet:71290) |
Familial thrombocytosis | (Orphanet:71493) |
Fanconi anemia | (Orphanet:84) |
Gray platelet syndrome | (Orphanet:721) |
Hereditary neutrophilia | (Orphanet:279943) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hyper-IgM syndrome type 4 | (Orphanet:101091) |
Kostmann syndrome | (Orphanet:99749) |
MONOSOMY 7 OF BONE MARROW | (OMIM:252270) |
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY | (OMIM:601347) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality | (Orphanet:86841) |
Myelodysplastic syndromes | (Orphanet:52688) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Platelet storage pool disease | (Orphanet:98454) |
Polycythemia vera | (Orphanet:729) |
Relapsing polychondritis | (Orphanet:728) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Rothmund-Thomson syndrome type 2 | (Orphanet:221016) |
Shwachman-Diamond syndrome | (Orphanet:811) |