Human Gene Set: HP_PATHOLOGICAL_INCLUSION_BODY


Standard name HP_PATHOLOGICAL_INCLUSION_BODY
Systematic name M50930
Brief description Pathological inclusion body
Full description or abstract Pathological inclusion bodies are are composed of glycogen, proteins, nucleic acids, lipids, hemosiderin, and calcium, that accumulate as metabolic by-products, catabolic products of macromolecular complexes, or in the context of cell injury. []
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:6001025
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:6001025
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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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