Autoimmune hemolytic anemia, cold type
General Information (adopted from Orphanet):
| Synonyms, Signs: |
cAHA Cold AIHA cAIHA |
| Number of Symptoms | 7 |
| OrphanetNr: | 228312 |
| OMIM Id: |
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| ICD-10: |
D59.1 |
| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
398937006 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Multifactorial [Orphanet] |
| Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Autoimmune hemolytic anemia
-Rare hematologic disease |
Symptom Information:
|
|
(HPO:0001744) | Splenomegaly | Frequent [Orphanet] | 337 / 7739 | |||
|
|
(HPO:0000980) | Pallor | Very frequent [Orphanet] | 52 / 7739 | |||
|
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(HPO:0001877) | Abnormality of erythrocytes | Very frequent [Orphanet] | 18 / 7739 | |||
|
|
(HPO:0001878) | Hemolytic anemia | Frequent [Orphanet] | 83 / 7739 | |||
|
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(HPO:0002093) | Respiratory insufficiency | Very frequent [Orphanet] | 410 / 7739 | |||
|
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(HPO:0002960) | Autoimmunity | Very frequent [Orphanet] | 78 / 7739 | |||
|
|
(HPO:0001324) | Muscle weakness | Very frequent [Orphanet] | 859 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|