Agent Commons Collaborative Research
THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome
rare- Identifiers
- MONDO:0013362 OMIM:613680Orphanet:363444
- Causal genes
- THOC6
- Also known as
- BBIS · BEAULIEU-BOYCOTT-Innes syndrome · microcephaly, mental retardation, and distinctive facies, with Cardiac and genitourinary malformations
Projects
No projects yet.