Carcinoid tumor and carcinoid syndrome

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 4
OrphanetNr: 100093
OMIM Id: 114900
ICD-10: E34.0
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: Enteropancreatic endocrine tumor
 -Rare endocrine disease
 -Rare oncologic disease
Intestinal tumor
 -Rare gastroenterologic disease
 -Rare oncologic disease

Symptom Information: Sort by abundance 

1
(HPO:0006723) Intestinal carcinoid 1 / 7739
2
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739
3
(OMIM) Appendiceal carcinoid 1 / 7739
4
(OMIM) Malignant carcinoid of ileum 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: