Any holoprosencephaly in which the cause of the disease is a mutation in the PTCH1 gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
holoprosencephaly 3
MONDO:0007733
holoprosencephaly 4
MONDO:0007734
holoprosencephaly 2
MONDO:0007999
holoprosencephaly 1
MONDO:0009349
holoprosencephaly 6
MONDO:0011616
holoprosencephaly 8
MONDO:0012267