Neuroendocrine neoplasm of appendix

Endocrine tumor of the appendix is the most common sporadic neoplasm of the appendix and the second most common type of digestive endocrine tumor, often with no specific clinical presentation. They are divided into either classic endocrine tumor of the appendix or the more aggressive goblet cell carcinoma (GCC; see these terms).



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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)		 PMID
(PMCID)
        

Phenotype(s) retrieved from Orphanet

    Total: 30

HPO ID Term Frequency
HP:0006723 Intestinal carcinoid Obligate (100%)
HP:0002017 Nausea and vomiting Frequent (79-30%)
HP:0002574 Episodic abdominal pain Frequent (79-30%)
HP:0004396 Poor appetite Frequent (79-30%)
HP:0005249 Functional intestinal obstruction Frequent (79-30%)
HP:0010676 Mechanical ileus Frequent (79-30%)
HP:0011848 Abdominal colic Frequent (79-30%)
HP:0012701 Bowel urgency Frequent (79-30%)
HP:0030142 Abnormal bowel sounds Frequent (79-30%)
HP:0030144 Hypoactive bowel sounds Frequent (79-30%)
HP:0002019 Constipation Occasional (29-5%)
HP:0002039 Anorexia Occasional (29-5%)
HP:0002240 Hepatomegaly Occasional (29-5%)
HP:0002730 Chronic noninfectious lymphadenopathy Occasional (29-5%)
HP:0002910 Elevated hepatic transaminase Occasional (29-5%)
HP:0003148 Elevated serum acid phosphatase Occasional (29-5%)
HP:0004385 Protracted diarrhea Occasional (29-5%)
HP:0030412 Ileal adenocarcinoma Occasional (29-5%)
HP:0040276 Adenocarcinoma of the colon Occasional (29-5%)
HP:0001579 Primary hypercortisolism Very rare (4-1%)
HP:0001962 Palpitations Very rare (4-1%)
HP:0002099 Asthma Very rare (4-1%)
HP:0002615 Hypotension Very rare (4-1%)
HP:0003144 Increased serum serotonin Very rare (4-1%)
HP:0005211 Midgut malrotation Very rare (4-1%)
HP:0010446 Tricuspid stenosis Very rare (4-1%)
HP:0011749 Adrenocorticotropic hormone excess Very rare (4-1%)
HP:0030148 Heart murmur Very rare (4-1%)
HP:0031499 Appendiceal mucinous neoplasm Very rare (4-1%)
HP:0100615 Ovarian neoplasm Very rare (4-1%)


Phenotype(s) retrieved from case reports

    Total: 0

HPO ID Term # of case reports


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID