Drug-induced autoimmune hemolytic anemia
General Information (adopted from Orphanet):
|
Synonyms, Signs:
|
Drug-induced AIHA
|
|
Number of Symptoms
|
10
|
|
OrphanetNr:
|
90037
|
|
OMIM Id:
|
|
|
ICD-10:
|
D59.0
|
|
UMLs:
|
C0391817
|
|
MeSH:
|
|
|
MedDRA:
|
|
|
Snomed:
|
309742004
|
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
|
|
|
|
|
|
|
|
|
|
|
1
|
(HPO:0012086)
|
Abnormal urinary color |
Occasional [Orphanet]
|
|
|
|
19 / 7739
|
|
2
|
(HPO:0002315)
|
Headache |
Very frequent [Orphanet]
|
|
|
|
175 / 7739
|
|
3
|
(HPO:0001396)
|
Cholestasis |
Occasional [Orphanet]
|
|
|
|
136 / 7739
|
|
4
|
(HPO:0001744)
|
Splenomegaly |
Occasional [Orphanet]
|
|
|
|
337 / 7739
|
|
5
|
(HPO:0000980)
|
Pallor |
Very frequent [Orphanet]
|
|
|
|
52 / 7739
|
|
6
|
(HPO:0011675)
|
Arrhythmia |
Occasional [Orphanet]
|
|
|
|
226 / 7739
|
|
7
|
(HPO:0001635)
|
Congestive heart failure |
Occasional [Orphanet]
|
|
|
|
232 / 7739
|
|
8
|
(HPO:0001877)
|
Abnormality of erythrocytes |
Very frequent [Orphanet]
|
|
|
|
18 / 7739
|
|
9
|
(HPO:0002093)
|
Respiratory insufficiency |
Very frequent [Orphanet]
|
|
|
|
410 / 7739
|
|
10
|
(HPO:0001324)
|
Muscle weakness |
Very frequent [Orphanet]
|
|
|
|
859 / 7739
|
ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |