Microphthalmia, syndromic 12
Also known as RARB syndromic microphthalmia, microphthalmia, syndromic type 12, syndromic microphthalmia caused by mutation in RARB, MCOPS12+2 more
RARB syndromic microphthalmia, microphthalmia, syndromic type 12, syndromic microphthalmia caused by mutation in RARB, MCOPS12, microphthalmia with or without pulmonary hypoplasia, diaphragmatic hernia, and/or Cardiac defects, syndromic microphthalmia-12.
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.
RARB syndromic microphthalmia, microphthalmia, syndromic type 12, syndromic microphthalmia caused by mutation in RARB, MCOPS12, microphthalmia with or without pulmonary hypoplasia, diaphragmatic hernia, and/or Cardiac defects, syndromic microphthalmia-12
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.