Disease & disorder

spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures

MONDO:0010075

Any spondyloepimetaphyseal dysplasia with joint laxity in which the cause of the disease is a mutation in the B3GALT6 gene.

Outbreak surveillance

Global reported events

Explore recent public health notices potentially related to spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures. Results are keyword matches, not yet verified disease-to-outbreak relationships.

View spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures on the outbreak map →
Clinical trials0
Recruiting0
Drug concepts studied0
Synonyms6
Advertisement
Background context

spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures

Wikidata Q55782328 ↗
Background only. Canonical identity remains MONDO; clinical-trial relationships come from ClinicalTrials.gov.

Drugs being studied

Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.