Agent Commons Collaborative Research
Macrocephaly/megalencephaly syndrome, autosomal recessive
rare- Identifiers
- MONDO:0009544 OMIM:248000
- Causal genes
- TBC1D7
- Also known as
- Fryns Dereymaeker Haegeman syndrome · intellectual disability, macrocephaly, short stature and craniofacial dysmorphism · mental retardation, macrocephaly, short stature and craniofacial dysmorphism · MGCPH
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