Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome
Also known as SMED short limb-hand type, SMED type 2, Smed short limb-abnormal calcification type, Smed, short limb-abnormal calcification type+9 more
SMED short limb-hand type, SMED type 2, Smed short limb-abnormal calcification type, Smed, short limb-abnormal calcification type, Smed, short limb-hand type, Smed, type 2, Smed-SL, Smed-SL/Ac, spondyloepimetaphyseal dysplasia - short limb - abnormal calcification, spondylometaepiphyseal dysplasia short limb-abnormal calcification type, spondylometaepiphyseal dysplasia short limb-hand type, spondylometaepiphyseal dysplasia, short limb-abnormal calcification type, spondylometaepiphyseal dysplasia, short limb-hand type.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
SMED short limb-hand type, SMED type 2, Smed short limb-abnormal calcification type, Smed, short limb-abnormal calcification type, Smed, short limb-hand type, Smed, type 2, Smed-SL, Smed-SL/Ac, spondyloepimetaphyseal dysplasia - short limb - abnormal calcification, spondylometaepiphyseal dysplasia short limb-abnormal calcification type, spondylometaepiphyseal dysplasia short limb-hand type, spondylometaepiphyseal dysplasia, short limb-abnormal calcification type, spondylometaepiphyseal dysplasia, short limb-hand type
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.