Hepatocellular clear cell carcinoma

Summary

Hepatocellular clear cell carcinoma (MONDO:0003243) is a cancer. A subtype of clear cell adenocarcinoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Classification: Cancer

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	hepatocellular clear cell carcinoma
Mondo ID	MONDO:0003243
DOID	DOID:5016
NCIT	C5754
UMLS	C1266020
MedGen	690059
GARD	0023418
Is cancer (heuristic)	yes

Also known as: clear cell carcinoma of liver cells · clear cell carcinoma of the liver cells · clear cell hepatocellular cancer · clear cell hepatocellular carcinoma · hepatocellular clear cell carcinoma · liver cell clear cell carcinoma

Disease family

This is a subtype of clear cell adenocarcinoma. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › carcinoma › adenocarcinoma › clear cell adenocarcinoma › hepatocellular clear cell carcinoma

Related subtypes (10): fallopian tube clear cell adenocarcinoma, bladder clear cell adenocarcinoma, urethra clear cell adenocarcinoma, glycogen-rich clear cell breast carcinoma, extrahepatic bile duct clear cell adenocarcinoma, clear cell renal carcinoma, ovarian clear cell adenocarcinoma, cervical clear cell adenocarcinoma, endometrial clear cell adenocarcinoma, hidradenocarcinoma

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.