Erythrocyte macrocytosis
Symptom Information:
Symptom ID: | HPO:0005518 | |||
Synonyms: |
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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) Erythrocyte macrocytosis(HPO:0005518) MedDRA: |
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Database Frequency: | 13 / 7739 | |||
Resource: |
All diseases associated with this symptom:
DIAMOND-BLACKFAN ANEMIA 3 | (OMIM:610629) |
DIAMOND-BLACKFAN ANEMIA 6 | (OMIM:612561) |
DIAMOND-BLACKFAN ANEMIA 7 | (OMIM:612562) |
DIAMOND-BLACKFAN ANEMIA 8 | (OMIM:612563) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
INTRINSIC FACTOR DEFICIENCY | (OMIM:261000) |
MONOSOMY 7 OF BONE MARROW | (OMIM:252270) |
Methylcobalamin deficiency type cblDv1 | (Orphanet:308380) |
Methylmalonic acidemia with homocystinuria, type cblD | (Orphanet:79283) |
Methylmalonic acidemia with homocystinuria, type cblJ | (Orphanet:369955) |
Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
Pearson syndrome | (Orphanet:699) |
Vitamin B12-responsive methylmalonic acidemia, type cblDv2 | (Orphanet:308442) |