Clinical Signs and Symptoms
ORPHA:228123 Coccidioidomycosis
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.
- Fever HP:0001945
- Immunodeficiency HP:0002721
- Increased circulating IgG level HP:0003237
- Increased circulating IgM level HP:0003496
- Pneumonia HP:0002090
Frequent
- Abnormality of the nervous system HP:0000707
- Abscess HP:0025615
- Arthritis HP:0001369
- Atypical scarring of skin HP:0000987
- CSF lymphocytic pleiocytosis HP:0200149
- CSF pleocytosis HP:0012229
- Chest pain HP:0100749
- Cough HP:0012735
- Eosinophilia HP:0001880
- Erythema nodosum HP:0012219
- Exudative pleural effusion HP:0011921
- Fatigue HP:0012378
- Folliculitis HP:0025084
- Granuloma HP:0032252
- Hemoptysis HP:0002105
- Hypoglycorrhachia HP:0011972
- Increased CSF protein HP:0002922
- Indurated nodule HP:0032217
- Lymphadenopathy HP:0002716
- Mediastinal lymphadenopathy HP:0100721
- Morbilliform rash HP:0012282
- Myalgia HP:0003326
- Panniculitis HP:0012490
- Papule HP:0200034
- Parenchymal consolidation HP:0032177
- Pleural empyema HP:0011919
- Pruritus HP:0000989
- Pulmonary infiltrates HP:0002113
- Respiratory distress HP:0002098
- Skin plaque HP:0200035
- Skin rash HP:0000988
- Unusual CNS infection HP:0011450
- Urticarial plaque HP:0030351
- Verrucous papule HP:0012500
Occasional
- Abnormal retinal morphology HP:0000479
- Abnormal sperm morphology HP:0012864
- Abnormality of blood and blood-forming tissues HP:0001871
- Abnormality of long bone morphology HP:0011314
- Abnormality of the bladder HP:0000014
- Abnormality of the endocrine system HP:0000818
- Abnormality of the female genitalia HP:0010460
- Abnormality of the genitourinary system HP:0000119
- Abnormality of the kidney HP:0000077
- Abnormality of the liver HP:0001392
- Abnormality of the male genitalia HP:0010461
- Abnormality of the metacarpal bones HP:0001163
- Abnormality of the spleen HP:0001743
- Abnormality of the vertebral column HP:0000925
- Blurred vision HP:0000622
- Broad metatarsal HP:0001783
- Broad ribs HP:0000885
- Broad skull HP:0002682
- Cerebral ischemia HP:0002637
- Coccidioidal meningitis HP:0032161
- Cognitive impairment HP:0100543
- Headache HP:0002315
- Hearing impairment HP:0000365
- Hydrocephalus HP:0000238
- Invasive fungal infection HP:0020101
- Nuchal rigidity HP:0031179
- Osteolysis HP:0002797
- Osteomyelitis HP:0002754
- Pancreatitis HP:0001733
- Pericarditis HP:0001701
- Peritonitis HP:0002586
- Personality changes HP:0000751
- Photophobia HP:0000613
- Renal insufficiency HP:0000083
- Seizures HP:0001250
- Vasculitis HP:0002633
- Vasospasm HP:0025637
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.