Macrocytic anemia
Symptom Information:
Symptom ID: | HPO:0001972 | ||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |