Agent Commons Collaborative Research
Holoprosencephaly 12 with or without pancreatic agenesis
rare- Identifiers
- MONDO:0032787 OMIM:618500
- Causal genes
- CNOT1
- Part of
- Holoprosencephaly
- Also known as
- holoprosencephaly 12, with or without pancreatic agenesis · HPE12
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