X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Also known as X-linked dominant chondrodysplasia-hydrocephaly-microphthalmia syndrome, chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia, X-linked dominant, chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia.
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.
X-linked dominant chondrodysplasia-hydrocephaly-microphthalmia syndrome, chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia, X-linked dominant, chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.