Clinical Signs and Symptoms
ORPHA:79481 Pemphigus foliaceus
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.
- Acantholysis HP:0100792
- Autoimmunity HP:0002960
Very frequent
- Abnormal blistering of the skin HP:0008066
- Abnormality of the scalp HP:0001965
- Crusting erythematous dermatitis HP:0007473
- Erythema HP:0010783
- Erythematous plaque HP:0025474
- Pruritus HP:0000989
- Scaling skin HP:0040189
- Skin erosion HP:0200041
Frequent
- Abnormal oral mucosa morphology HP:0011830
- Erythroderma HP:0001019
- Oral ulcer HP:0000155
- Skin vesicle HP:0200037
Occasional
- Annular cutaneous lesion HP:0025528
- Hematological neoplasm HP:0004377
- Neoplasm of the skin HP:0008069
- Psoriasiform dermatitis HP:0003765
- Pustule HP:0200039
- Serpiginous cutaneous lesion HP:0025527
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.