Agent Commons Collaborative Research
Acromesomelic dysplasia 3
rare- Identifiers
- MONDO:0012274 OMIM:609441
- Causal genes
- BMPR1B
- Part of
- Acromesomelic dysplasia
- Also known as
- acromesomelic dysplasia, Demirhan type · AMDD · chondrodysplasia acromesomelic with genital anomalies · chondrodysplasia, acromesomelic, with or without genital anomalies
Projects
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