Symbrachydactyly of hand and foot, bilateral

Summary

Symbrachydactyly of hand and foot, bilateral (MONDO:0017520) is a disease. A subtype of symbrachydactyly of hands and feet — 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	symbrachydactyly of hand and foot, bilateral
Mondo ID	MONDO:0017520
Orphanet	295138
UMLS	C2919807
MedGen	754111
GARD	0025108
Is cancer (heuristic)	no

Disease family

This is a subtype of symbrachydactyly of hands and feet. 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 › disease of genetic or genomic mechanism › hereditary disease › brachydactyly › non-syndromic brachydactyly › symbrachydactyly of hands and feet › symbrachydactyly of hand and foot, bilateral

Related subtypes (1): symbrachydactyly of hand and foot, unilateral

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.