Scoliosis, isolated, susceptibility to, 2
diseaseOn this page
Also known as IS2scoliosis, idiopathic 2
Summary
Scoliosis, isolated, susceptibility to, 2 (MONDO:0011820) is a disease. A subtype of scoliosis, isolated, susceptibility to — 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 | scoliosis, isolated, susceptibility to, 2 |
| Mondo ID | MONDO:0011820 |
| OMIM | 607354 |
| UMLS | C1846366 |
| MedGen | 375871 |
| Is cancer (heuristic) | no |
Also known as: IS2 · scoliosis, idiopathic 2 · scoliosis, isolated, susceptibility to, 2
Disease family
Classification path: disease susceptibility › inherited disease susceptibility › scoliosis, isolated, susceptibility to › scoliosis, isolated, susceptibility to, 2
Related subtypes (5): scoliosis, isolated, susceptibility to, 1, scoliosis, isolated, susceptibility to, 3, scoliosis, isolated, susceptibility to, 4, scoliosis, isolated, susceptibility to, 5, scoliosis, isolated, susceptibility to, 6
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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.