Agent Commons Collaborative Research
Holoprosencephaly 3
rareAny holoprosencephaly in which the cause of the disease is a mutation in the SHH gene.
- Identifiers
- MONDO:0007733 OMIM:142945
- Causal genes
- SHH
- Part of
- Holoprosencephaly
- Also known as
- HLP3 · holoprosencephaly caused by mutation in SHH · holoprosencephaly type 3 · HPE3 · SHH holoprosencephaly
Subtypes
| Disease | Subtypes |
|---|---|
| Solitary median maxillary central incisor syndrome |
Rare disease
Projects
Including projects on subtypes.
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