Schizoid personality disorder

disease
On this page

Summary

Schizoid personality disorder (MONDO:0001161) is a disease with 1 GWAS associations across 3 studies. A subtype of personality disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • GWAS associations: 1

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameschizoid personality disorder
Mondo IDMONDO:0001161
MeSHD012557
DOIDDOID:10936
ICD-10-CMF60.1
ICD-111524611454
NCITC92631
SNOMED CT52954000
UMLSC0036339
MedGen20662
Is cancer (heuristic)no

Data availability: 1 GWAS association (3 studies).

Disease family

This is a subtype of personality disorder. 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 developmental or physiological process › psychiatric disorderpersonality disorderschizoid personality disorder

Related subtypes (9): schizotypal personality disorder, borderline personality disorder, dependent personality disorder, obsessive-compulsive personality disorder, paranoid personality disorder, antisocial personality disorder, avoidant personality disorder, narcissistic personality disorder, histrionic personality disorder

Genetics & variants

GWAS landscape

1 GWAS associations across 3 studies. Top hits map to 1 distinct genes (as reported by GWAS).

Top associations by p-value

rsIDp-valueGeneRisk alleleOdds ratio
rs5375497047e-12LINC02782C3.12

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST90481792Verma A20241,772448,169Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90480757Verma A2024385121,112Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90481791Verma A2024385121,112Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.

Variant details and genetic-evidence tiers

Tier distribution (top 50 variants)

TierVariants
Tier 1: coding0
Tier 2: splice/UTR0
Tier 3: regulatory0
Tier 4: intronic/intergenic1

MAF distribution

BucketVariants
common (>=0.05)0
low_freq (0.01-0.05)0
rare (<0.01)1
unknown0

Functional consequences

ConsequenceCount
intron_variant1

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
rs53754970415086791C>T0intron_variantLINC027827e-12Tier 4: intronic/intergenic

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.