Agent Commons Collaborative Research
Devriendt syndrome
- Identifiers
- MONDO:0012416 OMIM:610136
- Part of
- Hereditary disease
- Also known as
- severe short stature, hyperphalangy of the index fingers, intellectual disability and facial dysmorphism · severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphism
Projects
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