Clinical Signs and Symptoms
ORPHA:199241 Pulmonary capillary hemangiomatosis
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.
- Capillary malformation HP:0025104
- Decreased DLCO HP:0045051
- Ground-glass opacification on pulmonary HRCT HP:0025179
- Interlobular septal thickening on pulmonary HRCT HP:0030879
- Lymphadenopathy HP:0002716
- Pulmonary capillary hemangiomatosis HP:0005954
Very frequent
- Abnormal pulmonary vein morphology HP:0030968
- Centrilobular ground-glass opacification on pulmonary HRCT HP:0025180
- Clubbing of fingers HP:0100759
- Cyanosis HP:0000961
- Diffuse alveolar hemorrhage HP:0025420
- Dyspnea HP:0002094
- Elevated pulmonary artery pressure HP:0004890
- Exertional dyspnea HP:0002875
- Hemoptysis HP:0002105
- Hemothorax HP:0012151
- Hypoxemia HP:0012418
- Mediastinal lymphadenopathy HP:0100721
- Pedal edema HP:0010741
- Right ventricular failure HP:0001708
Frequent
- Pleural effusion HP:0002202
- Pulmonary edema HP:0100598
Occasional
- Pericardial effusion HP:0001698
Rare
- Antinuclear antibody positivity HP:0003493
- Cytoplasmic antineutrophil antibody positivity HP:0032230
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.