Appendix mucinous cystadenocarcinoma

disease
On this page

Also known as appendiceal colloid cystadenocarcinomaappendiceal colloidal cystadenocarcinomaappendiceal mucinous cystadenocarcinomaappendix colloid cystadenocarcinomaappendix colloidal cystadenocarcinomacolloid cystadenocarcinoma of appendixcolloid cystadenocarcinoma of the appendixcolloidal cystadenocarcinoma of appendixcolloidal cystadenocarcinoma of the appendixmucinous cystadenocarcinoma of appendixmucinous cystadenocarcinoma of the appendixvermiform appendix mucinous cystadenocarcinoma

Summary

Appendix mucinous cystadenocarcinoma (MONDO:0002703) is a disease. A subtype of mucinous cystadenocarcinoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameappendix mucinous cystadenocarcinoma
Mondo IDMONDO:0002703
DOIDDOID:3607
NCITC5511
UMLSC1096639
MedGen204256
GARD0023218
Anatomy (UBERON)UBERON:0001154
Is cancer (heuristic)no

Also known as: appendiceal colloid cystadenocarcinoma · appendiceal colloidal cystadenocarcinoma · appendiceal mucinous cystadenocarcinoma · appendix colloid cystadenocarcinoma · appendix colloidal cystadenocarcinoma · appendix mucinous cystadenocarcinoma · colloid cystadenocarcinoma of appendix · colloid cystadenocarcinoma of the appendix · colloidal cystadenocarcinoma of appendix · colloidal cystadenocarcinoma of the appendix · mucinous cystadenocarcinoma of appendix · mucinous cystadenocarcinoma of the appendix · vermiform appendix mucinous cystadenocarcinoma

Disease family

Classification path: human disease › disease by etiologic mechanism › cancer or benign tumorneoplastic disease or syndromeneoplasmcancercarcinomaadenocarcinomamucinous adenocarcinoma › mucinous cystadenocarcinoma › appendix mucinous cystadenocarcinoma

Related subtypes (3): ovarian mucinous cystadenocarcinoma, breast mucinous cystadenocarcinoma, pancreatic mucinous cystadenocarcinoma

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 0.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.