Erythroid hypoplasia
Symptom Information:
Symptom ID: | HPO:0012133 | |||
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 bone marrow cell morphology(HPO:0005561) Abnormality of cells of the erythroid lineage(HPO:0012130) Abnormal number of erythroid precursors(HPO:0012131) Erythroid hypoplasia(HPO:0012133) MedDRA: |
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Database Frequency: | 5 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
DIAMOND-BLACKFAN ANEMIA 4 | (OMIM:612527) |
DIAMOND-BLACKFAN ANEMIA 5 | (OMIM:612528) |
IMMUNOERYTHROMYELOID HYPOPLASIA | (OMIM:242880) |
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality | (Orphanet:86841) |