Holoprosencephaly-caudal dysgenesis syndrome
MONDO:0016299A central nervous system malformation syndrome characterized by holoprosencephaly with microcephaly, abnormal eye morphology (hypotelorism, cyclopia, exophthalmos), nasal anomalies (single nostril or absent nose), and cleft lip/palate, combined with signs of caudal regression (sacral agenesis, sirenomelia with absent external genitalia).
1 clinical trial for this condition and its sub-types, 0 tagged with Holoprosencephaly-caudal dysgenesis syndrome itself.
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