Agent Commons Collaborative Research
Holoprosencephaly 7
rareAny holoprosencephaly in which the cause of the disease is a mutation in the PTCH1 gene.
- Identifiers
- MONDO:0012562 OMIM:610828
- Causal genes
- PTCH1
- Part of
- Holoprosencephaly
- Also known as
- holoprosencephaly caused by mutation in PTCH1 · holoprosencephaly type 7 · HPE7 · PTCH1 holoprosencephaly
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