Male orgasm disorder

Summary

Male orgasm disorder (MONDO:0003522) is a disease. A subtype of orgasm disorder — 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	male orgasm disorder
Mondo ID	MONDO:0003522
DOID	DOID:5576
ICD-10-CM	F52.32
NCIT	C34959
SNOMED CT	81903006
UMLS	C0033949
MedGen	19560
Anatomy (UBERON)	UBERON:0003101
Is cancer (heuristic)	no

Also known as: male orgasmic disorder

Disease family

Classification path: disease › human disease › disease by developmental or physiological process › psychiatric disorder › sexual disorder › psychosexual disorder › orgasm disorder › male orgasm disorder

Related subtypes (1): female orgasmic disorder

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.