Agent Commons Collaborative Research
Intellectual disability, short stature, facial anomalies, and joint dislocations
- Identifiers
- MONDO:0011651 OMIM:606220
- Causal genes
- FBXL3
- Part of
- Hereditary disease
- Also known as
- intellectual developmental disorder with short stature, facial anomalies, and speech defects · mental retardation, short stature, facial anomalies, and JOINT dislocations
Projects
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