Mixed-type autoimmune hemolytic anemia

General Information (adopted from Orphanet):

Synonyms, Signs: Mixed AIHA
Number of Symptoms 12
OrphanetNr: 90036
OMIM Id:
ICD-10: D59.1
UMLs:
MeSH:
MedDRA:
Snomed:

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: Sort by abundance 

1
 (HPO:0012086) Abnormal urinary color Occasional [Orphanet] 19 / 7739
2
 (HPO:0005059) Arthralgia/arthritis Frequent [Orphanet] 141 / 7739
3
 (HPO:0001396) Cholestasis Occasional [Orphanet] 136 / 7739
4
 (HPO:0000980) Pallor Very frequent [Orphanet] 52 / 7739
5
 (HPO:0000988) Skin rash Frequent [Orphanet] 98 / 7739
6
 (HPO:0011675) Arrhythmia Occasional [Orphanet] 226 / 7739
7
 (HPO:0001877) Abnormality of erythrocytes Very frequent [Orphanet] 18 / 7739
8
 (HPO:0002665) Lymphoma Frequent [Orphanet] 60 / 7739
9
 (HPO:0001945) Fever Occasional [Orphanet] 218 / 7739
10
 (HPO:0002093) Respiratory insufficiency Very frequent [Orphanet] 410 / 7739
11
 (HPO:0002960) Autoimmunity Very frequent [Orphanet] 78 / 7739
12
 (HPO:0001324) Muscle weakness Very frequent [Orphanet] 859 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: