Autoimmune hemolytic anemia

General Information (adopted from Orphanet):

Synonyms, Signs: AHA
AIHA
Number of Symptoms 16
OrphanetNr: 98375
OMIM Id:
ICD-10: D59.0
D59.1
UMLs: C0002880
MeSH: D000744
MedDRA: 10002046
Snomed: 413603009

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: Rare acquired hemolytic anemia
 -Rare hematologic disease

Symptom Information: Sort by abundance 

1
 (HPO:0012086) Abnormal urinary color Occasional [Orphanet] 19 / 7739
2
 (HPO:0002315) Headache Very frequent [Orphanet] 175 / 7739
3
 (HPO:0002027) Abdominal pain Occasional [Orphanet] 184 / 7739
4
 (HPO:0001744) Splenomegaly Occasional [Orphanet] 337 / 7739
5
 (HPO:0001396) Cholestasis Frequent [Orphanet] 136 / 7739
6
 (HPO:0000980) Pallor Very frequent [Orphanet] 52 / 7739
7
 (HPO:0001635) Congestive heart failure Occasional [Orphanet] 232 / 7739
8
 (HPO:0011675) Arrhythmia Occasional [Orphanet] 226 / 7739
9
 (HPO:0002665) Lymphoma Frequent [Orphanet] 60 / 7739
10
 (HPO:0001877) Abnormality of erythrocytes Very frequent [Orphanet] 18 / 7739
11
 (HPO:0001878) Hemolytic anemia Very frequent [Orphanet] 83 / 7739
12
 (HPO:0001945) Fever Occasional [Orphanet] 218 / 7739
13
 (HPO:0002093) Respiratory insufficiency Very frequent [Orphanet] 410 / 7739
14
 (HPO:0010978) Abnormality of immune system physiology Frequent [Orphanet] 148 / 7739
15
 (HPO:0002960) Autoimmunity Very frequent [Orphanet] 78 / 7739
16
 (HPO:0001324) Muscle weakness Very frequent [Orphanet] 859 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: