Macrocytic anemia

Symptom Information:

Symptom ID: HPO:0001972
Synonyms:
Macrocytic anemia (disorder) [Orphanet:48260]
Anemia, Macrocytic [Orphanet:48260]
Macrocytic anemia [OMIM:Macrocytic anemia]
Macrocytic anemia [Orphanet:48260]
Anaemia macrocytic [Orphanet:48260]
Anaemia macrocytic [MedDRA:10002064]
Anemia macrocytic [MedDRA:10002064]
Macrocytic anaemia NOS [MedDRA:10002064]
Macrocytic anemia [MedDRA:10002064]
Macrocytic anaemia [MedDRA:10002064]
Anemia, macrocytic [OMIM:Anemia, macrocytic]
Macrocytic anemia (folate or rarely B12 deficiency) [OMIM:Macrocytic anemia (folate or rarely B12 deficiency)]
Quality:
Cross references:
Orphanet:48260 "Macrocytic anemia" [Orphanet:48260]
OMIM: "Macrocytic anemia" [OMIM:Macrocytic anemia]
OMIM: "Anemia, macrocytic" [OMIM:Anemia, macrocytic]
OMIM: "Macrocytic anemia (folate or rarely B12 deficiency)" [OMIM:Macrocytic anemia (folate or rarely B12 deficiency)]
UMLS:C0002886 "Anemia, Macrocytic" [Orphanet:48260]
Is a (Direct Parents):
Orphanet Anemia
MedDRA Vitamin deficiencies NEC
HPO         Anemia of inadequate production
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)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Vitamin related disorders(MedDRA:10047635)
       Vitamin deficiencies NEC(MedDRA:10047627)
          Macrocytic anemia(HPO:0001972)
Database Frequency: 26 / 7739
Resource:

All diseases associated with this symptom:

16q24.3 microdeletion syndrome (Orphanet:261250)
AARSKOG SYNDROME, AUTOSOMAL DOMINANT (OMIM:100050)
Aarskog-Scott syndrome (Orphanet:915)
Acute infantile liver failure-multisystemic involvement syndrome (Orphanet:370088)
Blackfan-Diamond anemia (Orphanet:124)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
CHROMOSOME 15q25 DELETION SYNDROME (OMIM:614294)
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18 (OMIM:615578)
Cartilage-hair hypoplasia (Orphanet:175)
Congenital dyserythropoietic anemia type III (Orphanet:98870)
DIAMOND-BLACKFAN ANEMIA 10 (OMIM:613309)
DIAMOND-BLACKFAN ANEMIA 12 (OMIM:615550)
DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS (OMIM:300946)
DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS (OMIM:606164)
DIAMOND-BLACKFAN ANEMIA 3 (OMIM:610629)
DIAMOND-BLACKFAN ANEMIA 4 (OMIM:612527)
DIAMOND-BLACKFAN ANEMIA 5 (OMIM:612528)
DIAMOND-BLACKFAN ANEMIA 6 (OMIM:612561)
DIAMOND-BLACKFAN ANEMIA 7 (OMIM:612562)
DIAMOND-BLACKFAN ANEMIA 8 (OMIM:612563)
Pearson syndrome (Orphanet:699)
Shwachman-Diamond syndrome (Orphanet:811)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
Transcobalamin deficiency (Orphanet:859)
X-linked dyserythropoetic anemia with abnormal platelets and neutropenia (Orphanet:363727)
X-linked sideroblastic anemia (Orphanet:75563)