Holoprosencephaly 3

MONDO:0007733

Any holoprosencephaly in which the cause of the disease is a mutation in the SHH gene.

Also known as: HLP3, HPE3, SHH holoprosencephaly, Shh holoprosencephaly, holoprosencephaly 3, holoprosencephaly caused by mutation in SHH, holoprosencephaly caused by mutation in Shh, holoprosencephaly type 3

0 clinical trials for this condition and its sub-types, 0 tagged with Holoprosencephaly 3 itself.

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Sub-types of Holoprosencephaly 3

Solitary median maxillary central incisor syndrome 0 trials

Including sub-types (0) Tagged with Holoprosencephaly 3 (0)

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