Semilobar holoprosencephaly
MONDO:0700419A form of holoprosencephaly characterized by fusion of the left and right frontal and parietal lobes with only a posterior interhemispheric fissure. Craniofacial features variably include ocular hypotelorism, midline cleft lip (complete or partial) and a flat nose.
10 clinical trials for this condition and its sub-types.
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Disease
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Nervous system disorder
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Hereditary disease
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Endocrine system disorder
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Syndromic disease
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Hereditary endocrine growth disease
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Human disease
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Developmental defect during embryogenesis
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Hereditary neurological disease
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Disease of genetic or genomic mechanism
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