Megaloblastic bone marrow

Symptom Information:

Symptom ID: HPO:0001980
Synonyms:
Megaloblastic anemia [Orphanet:48280]
Megaloblastic anemia (disorder) [Orphanet:48280]
Anemia, Megaloblastic [Orphanet:48280]
Megaloblastic bone marrow [OMIM:Megaloblastic bone marrow]
Anaemia megaloblastic [Orphanet:48280]
Anaemia megaloblastic [MedDRA:10002065]
Anemia megaloblastic [MedDRA:10002065]
Megaloblastic anaemia NOS [MedDRA:10002065]
Megaloblastic anemia [MedDRA:10002065]
Megaloblastosis [MedDRA:10002065]
Other specified megaloblastic anaemias, not elsewhere classified [MedDRA:10002065]
Other specified megaloblastic anemias not elsewhere classified [MedDRA:10002065]
Other specified megaloblastic anemias, not elsewhere classified [MedDRA:10002065]
Megaloblastic anaemia [MedDRA:10002065]
Megaloblastosis [OMIM:Megaloblastosis]
Quality:
Cross references:
HPO:0001889 "Megaloblastic anemia" [Orphanet:48280]
Orphanet:48280 "Megaloblastic anemia" [Orphanet:48280]
OMIM: "Megaloblastic bone marrow" [OMIM:Megaloblastic bone marrow]
OMIM: "Megaloblastosis" [OMIM:Megaloblastosis]
UMLS:C0002888 "Anemia, Megaloblastic" [Orphanet:48280]
Is a (Direct Parents):
MedDRA Vitamin deficiencies NEC
Orphanet Anemia
HPO         Abnormality of multiple cell lineages in the bone marrow
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of bone marrow cell morphology(HPO:0005561)
             Abnormality of multiple cell lineages in the bone marrow(HPO:0012145)
                Megaloblastic bone marrow(HPO:0001980)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Vitamin related disorders(MedDRA:10047635)
       Vitamin deficiencies NEC(MedDRA:10047627)
          Megaloblastic bone marrow(HPO:0001980)
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Acute erythroid leukemia (Orphanet:318)
Pearson syndrome (Orphanet:699)
Transcobalamin deficiency (Orphanet:859)
Wolfram syndrome 1 (OMIM:222300)
Wolfram syndrome, mitochondrial form (OMIM:598500)