Holoprosencephaly 11

Definition

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

Also known as CDON holoprosencephaly, holoprosencephaly 11, holoprosencephaly caused by mutation in CDON, holoprosencephaly type 11, HPE11 — per MONDO

Also identified as

• DOID 0110877 per MONDO
• OMIM 614226 per MONDO
• UMLS C3280215 per MONDO