Clinical Signs and Symptoms
ORPHA:100077 Jejunal neuroendocrine tumor
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.
- Small intestine carcinoid HP:0006722
Always present
- Dermatological manifestations of systemic disorders HP:0001005
- Episodic abdominal pain HP:0002574
- Increased serum serotonin HP:0003144
- Intermittent diarrhea HP:0002254
Very frequent
- Abnormal bowel sounds HP:0030142
- Arterial occlusion HP:0025324
- Chronic fatigue HP:0012432
- Elevated hepatic transaminase HP:0002910
- Elevated serum acid phosphatase HP:0003148
- Episodic vomiting HP:0002572
- Extrahepatic cholestasis HP:0012334
- Functional intestinal obstruction HP:0005249
- Gastrointestinal obstruction HP:0004796
- Iron deficiency anemia HP:0001891
- Lymphadenopathy HP:0002716
- Nausea HP:0002018
- Weight loss HP:0001824
Frequent
- Intestinal fistula HP:0100819
Occasional
- Abnormality of the bronchi HP:0002109
- Arrhythmia HP:0011675
- Cardiogenic shock HP:0030149
- Edema HP:0000969
- Hepatic failure HP:0001399
- Hydronephrosis HP:0000126
- Hypotension HP:0002615
- Palpitations HP:0001962
- Pulmonic stenosis HP:0001642
- Right ventricular failure HP:0001708
- Tricuspid stenosis HP:0010446
- Zollinger-Ellison syndrome HP:0002044
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.