Band keratopathy

Summary

Band keratopathy (MONDO:0009016) is a disease. A subtype of corneal degeneration — 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

Field	Value
Canonical name	band keratopathy
Mondo ID	MONDO:0009016
MeSH	C562399
OMIM	217500
DOID	DOID:11164
ICD-10-CM	H18.42
ICD-11	184627034
NCIT	C118765
SNOMED CT	35055000
UMLS	C0155120
MedGen	56354
GARD	0024645
Is cancer (heuristic)	no

Also known as: band keratopathy · band-shaped keratopathy

Disease family

This is a subtype of corneal degeneration. 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 body system or component › disorder of orbital region › eye disorder › corneal disorder › corneal degeneration › band keratopathy

Related subtypes (4): phthisical cornea, peripheral degeneration of cornea, nodular degeneration of cornea, arcus senilis

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.