Human Gene Set: HP_THIN_CORPUS_CALLOSUM


Standard name HP_THIN_CORPUS_CALLOSUM
Systematic name M48892
Brief description Thin corpus callosum
Full description or abstract An abnormally thin corpus callous, due to atrophy, hypoplasia or agenesis. This term is intended to be used in situations where it is not known if thinning of the corpus callosum (for instance, as visualized by magnetic resonance tomography) is due to abnormal development (e.g. a leukodystrophy) or atrophy following normal development (e.g. neurodegeneration). [https://orcid.org/0000-0002-1735-8178]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0033725
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0033725
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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 2024.1.Hs: Updated to HPO Release 2024-04-26.

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