Clinical Signs and Symptoms
ORPHA:324636 Autoerythrocyte sensitization syndrome
The phenotypic description of this disease is based on an analysis of the biomedical literature and uses the terms of the Human Phenotype Ontology (HPO). Phenotypic abnormalities are presented by order of frequency of occurrence in the patient population, then by alphabetical order inside each frequency group.
- Bruising susceptibility HP:0000978
- Ecchymosis HP:0031364
Very frequent
- Abnormality of limbs HP:0040064
- Behavioral abnormality HP:0000708
- Pain HP:0012531
- Superficial dermal perivascular inflammatory infiltrate HP:0031190
Frequent
- Abnormality of the face HP:0000271
- Abnormality of the nervous system HP:0000707
- Anxiety HP:0000739
- Arthralgia HP:0002829
- Asthenia HP:0025406
- Borderline personality disorder HP:0012076
- Depressivity HP:0000716
- Diarrhea HP:0002014
- Edema HP:0000969
- Emotional lability HP:0000712
- Epigastric pain HP:0410019
- Epistaxis HP:0000421
- Erythematous plaque HP:0025474
- Fatigue HP:0012378
- Fever HP:0001945
- Headache HP:0002315
- Hematuria HP:0000790
- Impaired platelet adhesion HP:0008352
- Intramuscular hematoma HP:0012233
- Menorrhagia HP:0000132
- Myalgia HP:0003326
- Nausea HP:0002018
- Obsessive-compulsive trait HP:0008770
- Oral cavity bleeding HP:0030140
- Posttraumatic stress symptom HP:0033676
- Prolonged partial thromboplastin time HP:0003645
- Pruritus HP:0000989
- Self-injurious behavior HP:0100716
- Vertigo HP:0002321
- Vomiting HP:0002013
Occasional
- Abnormal erythrocyte morphology HP:0001877
- Autoimmune thrombocytopenia HP:0001973
- Gastrointestinal hemorrhage HP:0002239
- Intracranial hemorrhage HP:0002170
- Joint hemorrhage HP:0005261
- Thrombocytosis HP:0001894
Rare
Additional information
Further information
Specialised Social Services
Warning
The information provided is based on published scientific articles.
The information provided is estimated for the entire population of patients in routine care. Some phenotypic abnormalities reported here may occur individually with a variable temporality or severity, while others, not listed, may still be encountered. Phenotypic annotations are not yet available for all rare diseases; the annotation process is ongoing.
The information contained in Orphanet is regularly updated. It is possible that discoveries have been made since the last update and have not yet been incorporated.
Professionals are encouraged to always consult the latest scientific publications before making a decision based on the information provided. The information contained in Orphanet is not intended to replace the services of a healthcare professional. Orphanet cannot be held responsible for the deleterious, truncated or erroneous use of any information found in the Orphanet database.