Human Gene Set: HP_MILD_FETAL_VENTRICULOMEGALY


Standard name HP_MILD_FETAL_VENTRICULOMEGALY
Systematic name M49927
Brief description Mild fetal ventriculomegaly
Full description or abstract A kind of ventriculomegaly occurring in the fetal period and usually diagnosed by prenatal ultrasound. Cerebral ventriculomegaly is defined by atrial measurements 10 mm or more. Mild ventriculomegaly (MVM) is defined as measurements between 10 and 15 mm. Measurements are obtained from an axial plane at the level of the thalamic nuclei just below the standard image to measure the BPD (PMID:16100637). [https://orcid.org/0000-0002-0736-9199, PMID:16100637]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0010952
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External links https://hpo.jax.org/app/browse/term/HP:0010952
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
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Version history 2026.1.Hs: Updated to HPO Release 2026-01-08.


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