Heinz body anemia
General Information (adopted from Orphanet):
| Synonyms, Signs: |
|
| Number of Symptoms | 6 |
| OrphanetNr: | 178330 |
| OMIM Id: |
140700
|
| ICD-10: |
D58.2 |
| UMLs: |
C0700299 |
| MeSH: |
|
| MedDRA: |
10002058 |
| Snomed: |
|
Prevalence, inheritance and age of onset:
| Prevalence: | < 10 cases [Orphanet] |
| Inheritance: |
Autosomal dominant [Orphanet] |
| Age of onset: |
|
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Rare constitutional hemolytic anemia
-Rare genetic disease -Rare hematologic disease |
Symptom Information:
|
|
(HPO:0001930) | Nonspherocytic hemolytic anemia | 10 / 7739 | ||||
|
|
(HPO:0005511) | Heinz body anemia | 4 / 7739 | ||||
|
|
(HPO:0001939) | Abnormality of metabolism/homeostasis | 328 / 7739 | ||||
|
|
(OMIM) | Heat-labile hemoglobin | 1 / 7739 | ||||
|
|
(OMIM) | Heinz bodies in erythrocytes after splenectomy | 1 / 7739 | ||||
|
|
(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|