Myelodysplasia

Symptom Information:

Symptom ID: HPO:0002863
Synonyms:
Hypoplastic myelodysplasia [HPO:0002863]
Myelodysplastic syndrome [HPO:0002863]
Myelodysplastic syndrome [Orphanet:51090]
Myelodysplastic syndrome (disorder) [Orphanet:51090]
Myelodysplastic syndrome (morphologic abnormality) [Orphanet:51090]
Dysmyelopoietic Syndromes [Orphanet:51090]
Preleukemia [Orphanet:51090]
Hypoplastic myelodysplasia [OMIM:Hypoplastic myelodysplasia]
Myelodysplasia [OMIM:Myelodysplasia]
Myelodysplastic syndrome [OMIM:Myelodysplastic syndrome]
Myelodysplastic syndrome [MedDRA:10028533]
Marrow dysplasia [MedDRA:10028533]
Myelodysplasia [MedDRA:10028533]
Myelodysplastic syndrome NOS [MedDRA:10028533]
Myeloid dysplasia [MedDRA:10028533]
Preleukaemia [MedDRA:10028533]
Bone marrow dysplasia [MedDRA:10028533]
Preleukemia [MedDRA:10028533]
Osteomyelodysplasia [MedDRA:10028533]
MDS [MedDRA:10028533]
Myelodysplastic syndromes [MedDRA:10028536]
Quality:
Cross references:
Orphanet:51090 "Myelodysplastic syndrome" [Orphanet:51090]
OMIM: "Hypoplastic myelodysplasia" [OMIM:Hypoplastic myelodysplasia]
OMIM: "Myelodysplasia" [OMIM:Myelodysplasia]
OMIM: "Myelodysplastic syndrome" [OMIM:Myelodysplastic syndrome]
UMLS:C1963099 "Myelodysplasia" [HPO:0002863]
UMLS:C0026986 "Dysmyelopoietic Syndromes" [Orphanet:51090]
UMLS:C0033027 "Preleukemia" [Orphanet:51090]
Is a (Direct Parents):
Orphanet Haematological malignancy
HPO         Hematological neoplasm
MedDRA Leukemia
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)
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)