Megaloblastic anemia

Symptom Information:

Symptom ID: HPO:0001889
Synonyms:
Megaloblastic anemia (disorder) [Orphanet:48280]
Anemia, Megaloblastic [Orphanet:48280]
Megaloblastic anemia [OMIM:Megaloblastic anemia]
Megaloblastic anemia [Orphanet:48280]
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:0001980 "Megaloblastic bone marrow" [Orphanet:48280]
Orphanet:48280 "Megaloblastic anemia" [Orphanet:48280]
OMIM: "Megaloblastic anemia" [OMIM:Megaloblastic anemia]
OMIM: "Megaloblastosis" [OMIM:Megaloblastosis]
UMLS:C0002888 "Anemia, Megaloblastic" [Orphanet:48280]
Is a (Direct Parents):
HPO         Macrocytic anemia
MedDRA Vitamin deficiencies NEC
Orphanet Anemia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of erythrocytes(HPO:0001877)
             Anemia(HPO:0001903)
                Anemia of inadequate production(HPO:0010972)
                   Macrocytic anemia(HPO:0001972)
                      Megaloblastic anemia(HPO:0001889)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Vitamin related disorders(MedDRA:10047635)
       Vitamin deficiencies NEC(MedDRA:10047627)
          Megaloblastic anemia(HPO:0001889)
Database Frequency: 28 / 7739
Resource:

All diseases associated with this symptom:

3-phosphoglycerate dehydrogenase deficiency (Orphanet:79351)
Acute erythroid leukemia (Orphanet:318)
Congenital intrinsic factor deficiency (Orphanet:332)
Constitutional megaloblastic anemia with severe neurologic disease (Orphanet:319651)
Cystic fibrosis - gastritis - megaloblastic anemia (Orphanet:2575)
Formiminoglutamic aciduria (Orphanet:51208)
Gräsbeck-Imerslund disease (Orphanet:35858)
Hereditary folate malabsorption (Orphanet:90045)
Hereditary orotic aciduria (Orphanet:30)
Homocystinuria without methylmalonic aciduria (Orphanet:622)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
INTRINSIC FACTOR AND R BINDER, COMBINED CONGENITAL DEFICIENCY OF (OMIM:243320)
INTRINSIC FACTOR DEFICIENCY (OMIM:261000)
LESCH-NYHAN SYNDROME (OMIM:300322)
Lesch-Nyhan syndrome (Orphanet:510)
Methylcobalamin deficiency type cblDv1 (Orphanet:308380)
Methylcobalamin deficiency type cblE (Orphanet:2169)
Methylcobalamin deficiency type cblG (Orphanet:2170)
Methylmalonic acidemia with homocystinuria (Orphanet:26)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Methylmalonic acidemia with homocystinuria, type cblD (Orphanet:79283)
Methylmalonic acidemia with homocystinuria, type cblF (Orphanet:79284)
PERNICIOUS ANEMIA (OMIM:170900)
Permanent neonatal diabetes mellitus (Orphanet:99885)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
Vitamin B12-responsive methylmalonic acidemia, type cblDv2 (Orphanet:308442)
Wolfram syndrome 1 (OMIM:222300)
Wolfram syndrome, mitochondrial form (OMIM:598500)