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midline interhemispheric variant of holoprosencephaly
Disease Summary
Associated Targets (2)
Tchem
1
Tbio
1
Mondo Description Midline interhemispheric variant of holoprosencephaly (MIH) or syntelencephaly is a form of holoprosencephaly (HPE) characterized by non-separation of the posterior frontal and parietal lobes, normally-formed callosal genu and splenium, absence of the callosal body, normally-separated hypothalamus and lentiform nucleus, and frequent heterotopic gray matter.
Mondo Term and Equivalent IDs
MONDO:0019758: midline interhemispheric variant of holoprosencephaly