Human Gene Set: HP_ALOBAR_HOLOPROSENCEPHALY


Standard name HP_ALOBAR_HOLOPROSENCEPHALY
Systematic name M46121
Brief description Alobar holoprosencephaly
Full description or abstract A type of holoprosencephaly characterized by the presence of a single ventricle and no separation of the cerebral hemisphere. The single midline ventricle is often greatly enlarged. [HPO_CONTRIBUTOR:GC_HPE]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0006988
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0006988
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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
Dataset references  
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Version history 2023.1.Hs: Updated to HPO Release 2023-01-27.

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