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MIM:610828 - HOLOPROSENCEPHALY 7; HPE7
Xenbase Genes: ptch1
Human Disease Resource: MIM
| MONDO:0012562 - holoprosencephaly 7 |
| MONDO:0016296 - holoprosencephaly |
| DOID:0110876 - holoprosencephaly 7 |
|
| MONDO:0012562 - holoprosencephaly 7 |
| MONDO:0016296 - holoprosencephaly |
| DOID:0110876 - holoprosencephaly 7 |