Hereditary pyropoikilocytosis
General Information (adopted from Orphanet):
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Synonyms, Signs:
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Number of Symptoms
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4
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OrphanetNr:
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98867
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OMIM Id:
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141700
266140
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ICD-10:
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D58.1
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UMLs:
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C0520739
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MeSH:
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MedDRA:
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Snomed:
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9434008
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Prevalence, inheritance and age of onset:
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Prevalence:
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No data available.
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Inheritance:
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Age of onset:
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Disease classification (adopted from Orphanet):
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Parent Diseases:
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No data available.
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1
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(HPO:0005511)
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Heinz body anemia |
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4 / 7739
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2
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(HPO:0004445)
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Elliptocytosis |
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15 / 7739
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3
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(HPO:0001930)
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Nonspherocytic hemolytic anemia |
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10 / 7739
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4
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(HPO:0000006)
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Autosomal dominant inheritance |
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2518 / 7739
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ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |